Highlights
- The functional receptors of CBD and their distribution in oral cavity are briefly reviewed.
- The potentials of CBD in the treatment of several oral diseases are summarized.
- The administration routes of CBD are introduced to provide reference for the treatment of oral diseases.
- The challenges, related solutions and prospects of clinically applying CBD are discussed.
Abstract
Cannabidiol (CBD), one of the most important active ingredients in cannabis, has been reported to have some pharmacological effects such as antibacterial and analgesic effects, and to have therapeutic potential in the treatment of oral diseases such as oral cancer, gingivitis and periodontal diseases. However, there is a lack of relevant systematic research and reviews. Therefore, based on the etiology and clinical symptoms of several common oral diseases, this paper focuses on the therapeutic potential of CBD in periodontal diseases, pulp diseases, oral mucosal diseases, oral cancer and temporomandibular joint diseases. The pharmacological effects of CBD and the distribution and function of its receptors in the oral cavity are also summarized. In order to provide reference for future research and further clinical application of CBD, we also summarize several possible routes of administration and corresponding characteristics. Finally, the challenges faced while applying CBD clinically and possible solutions are discussed, and we also look to the future.
Graphical Abstract
Keywords
1. Introduction
In traditional Asian medicine, the cannabis plant is often used to treat toothaches, prevent dental caries and treat tumors without exploring the main active ingredients that are functioning. In recent years, with more and more in-depth studies, it has been found that the cannabis plant contains more than 400 molecules of medicinal value, about a quarter of which are cannabinoids [1]. And Δ9 tetrahydrocannabinol (Δ9-THC), cannabidiol (CBD) and cannabinol (CBN) are the three major cannabinoids that are most frequently discussed (Fig. 1 A-C). CBD and Δ9-THC are also the focus of research in recent years.
As the main representatives of plant cannabinoids, CBD and Δ9-THC play an important role in anti-inflammatory, analgesic, osteoporosis and cancer treatment [2]. Being different from the psychoactive Δ9-THC, CBD does not cause hallucinogenic addiction, and has been fully evaluated for drug safety, thus being approved by the FDA for the prevention and treatment of intractable epilepsy [3]. The chemical activity of CBD is mainly attributed to the hydroxyl group in the C-1′ and C-5′positions of the phenol ring, and the methyl group in the C-1 ′position of the cyclohexene ring and the amyl group in the C-3′position of the phenol ring [4]. Typically, through firstly synthesizing cannabigerolic acid (CBGA), and then combined with biochemical reactions, CBD can be gained. CBGA, derived from its aromatic precursor olivanic acid and surrounded by resorcinol with a carbon skeleton of different lengths, is the structural hallmark of plant cannabinoids and a key precursor for CBD synthesis [4]. To be exact, with the help of cannabidiolic acid(CBDA) synthetase, CBGA is converted into CBDA, which in turn generates CBD through a photochemical reaction, as shown in Fig. 1 D.
In recent years, relevant studies have revealed the important roles of CBD in bone tissue repair, oral health maintenance and cancer prevention and treatment. Particularly with the discovery of oral cannabinoid receptor (CBR), solid progress has been made in the study of applying CBD to oral diseases. However, considering the diversity of CBR’s distribution and activation mechanism, combined with the fact that there is a lack of research on CBD in the field of stomatology Therefore, based on the introduction of the distribution and function of CBR in the oral cavity, we review the therapeutic potential of CBD in periodontal diseases, pulp diseases, oral mucosal diseases, oral tumors and temporomandibular joint diseases in this paper. Furthermore, we discussed several possible routes of administration according to the pathogenesis and clinical characteristics of above oral diseases, aiming to provide reference for further application of CBD in oral diseases treatment. In addition, the difficulties and challenges that researchers may encounter while applying CBD and corresponding possible solutions are also presented. In conclusion, it is hoped that this review may inspire researchers to explore more innovated treatment methods aimed for oral diseases.
2. CBD and its receptors
2.1. Overview of pharmacological effects of CBD
Hemp, an annual herbaceous plant of the Mulberry family, has a long history of cultivation in China. And most of them are dioecious. CBD and Δ9-THC, the main chemical components of plant cannabinoids, play an important role in analgesia, anti-inflammatory [5], antioxidant [6], antidepressant [7], vasodilation [8], epilepsy, and cancer prevention. CBD has a low affinity for CB1 and CB2 receptors compared with Δ9-THC, and its safety and lack of psychoactivity making CBD a hot topic in recent years. CBD has many pharmacological effects in several pathological models, ranging from inflammatory and neurodegenerative diseases, to epilepsy, autoimmune diseases such as multiple sclerosis, arthritis, schizophrenia, and cancer(Table 1). As is known to all, CBD research mainly focuses on anti-anxiety and anti-depression aspects. For example, CBD was found to significantly reduce anxiety in patients due to its effects on the edge and marginal regions revealed by single photon emission computed tomography [9]. In addition, given its rare adverse reaction properties, it is also regarded as an drug to treat diseases such as cancer, inflammation and neurodegeneration. It exerts its effects as a painkiller [10], anticonvulsant [11], [12], anti-inflammatory, and antioxidant [13], [14]. In terms of anti-cancer, it has an inhibitory effect on breast cancer cells and can slow down the invasion of tumor cells to normal cells [15]. In terms of anti-inflammatory and acesodyne, CBD also shows significant potentials in mouse models [16]. CBD has also been shown to be a key factor in the treatment of tumor pain in patients who do not respond to opioids [17]. In addition, CBD in animal models of rheumatoid arthritis can also antagonize tumor necrosis factor-α (TNF-α) [18], increase A2A adenosine receptor signaling by inhibiting adenosine transporters, and prevent neurotoxicity and prion accumulation [19]. Furthermore, CBD possesses a powerful effect against methicillin-resistant Staphylococcus aureus [20]. In conclusion, based on current research, the possibility of using CBD for the treatment of cardiovascular diseases, cancer, arthritis, anxiety disorders, psychosis, epilepsy, neurodegenerative diseases (i. e., Alzheimer’s disease) and skin diseases is being explored [21], [22].
Table 1. Overview of CBD pharmacological effects.
Disease | Effects | References |
---|---|---|
Cancer | In a variety of cancer models, with anti-proliferation and anti-invasion effects; inhibits angiogenesis; enhances immune killing; induces autophagy-mediated cancer cell death; alleviates cancer pain; protects the body’s normal cells, etc. | [23], [24], [25], [26], [27], [28], [29] |
Infection | Inhibits the activity of Porphyromonas gingivalis; inhibit the activity of methicillin-resistant Staphylococcus aureus (Gram-positive bacteria or optionally anaerobic bacteria have a certain inhibitory effect) | [20], [30] |
Depression | Antidepressant effects in a genetic rodent model of depression. | [31], [32], [33] |
Anxiety disorder | Reduce patients’ social anxiety, relaxes muscle tension, improve patients’ sleep; reduces restlessness and inattention; regulates mu and delta opioid receptors in cerebral cortical membrane homogenate. | [3], [34], [35], [36], [37], [38] |
Pain | Treatment of patients with refractory central or peripheral nerve pain; attenuation of behavioral and glial changes in animal models of schizophrenia; analgesia and improvement of sleep quality in cancer patients. | [39], [40], [41] |
Epilepsy | Reduce the frequency of seizures, anticonvulsant. | [42], [43] |
Parkinson’s syndrome | Anti-inflammatory and antioxidant effects and neuroprotective effects; improves sleep, sedation and reduces mood swings. | [44], [45], [46] |
Rheumatoid arthritis | Inhibition of inflammatory TNF-alpha, reducing swelling and pain | [18], [30] |
Diabetic complications | Anti-inflammatory and antioxidant, protects peripheral nerves; reduces the risk of infection; improves cardiac function. | [47], [48], [49], [50] |
Cardiovascular disease | Anti-inflammatory and antioxidant slows heart muscle damage; reduces cardiovascular disease infection | [51], [52], [53] |
Alzheimer’s disease | Anti-inflammatory, antioxidant, and anti-apoptotic models of Aβ-induced neuroinflammation and neurodegeneration in vitro and in vivo. | [54], [55], [56], [57], [58], [59] |
Periodontal disease | In a rat model of periodontitis, alveolar bone absorption was slowed down;inhibits the expression of inflammatory NF-kB and inhibits the activity of periodontal microorganisms. | [60], [61], [62], [63], [64] |
2.2. Receptors of CBD
2.2.1. Cannabinoid receptor
As described in the study, two major cannabinoid receptors were discovered in the early 1990 s, namely cannabinoid type 1 (CB1) receptors and cannabinoid type 2 (CB2) receptors, which play an important role in mediating the biological effects of plant-derived and endogenous cannabinoids [65]. The CB1 and CB2 receptors share 44% homology in amino acid sequence, but differ in function. CB1 receptors are mainly expressed in the brain and central nervous system, while CB2 receptors in immune cells, microglia and brain neurons [66], [67]. CBD has been shown to be a weak agonist of CB1 receptors in humans, mice, and rats [68]. Despite its low affinity, studies have shown that CBD is a negative allosteric regulator of CB1 receptor, thus activating CB1 receptor, increasing ROS level and promoting inflammatory response [69], [70]. In contrast to CB1 receptors, activation of CB2 receptors by CBD leads to lower levels of ROS and TNF-α, which inhibits inflammation [70]. The anti-inflammatory activity of CBD can be antagonized by selective CB2 receptor antagonists. CBD acts on cannabinoid receptors, inhibits the activities of adenylate cyclase and voltage-gated calcium channels and activates potassium channels and mitogen-activated protein kinase (MAPK), inositol 3-phosphate kinase (PI3K) /AKT and mammalian rapamycin target (mTOR) signaling pathways, thus playing an important role in regulating cell survival, proliferation and apoptosis [71], [72].
2.2.2. GPR receptors
GPR55, a member of the orphan receptors, is involved in actin cytoskeleton processes during cells movement and migration [73]. This receptor has been reported to be associated with vascular function, motor coordination, metabolic disorders, bone physiology, pain, and cancer [74]. Studies have shown that GPR55 has a variety of biological regulatory functions such as: (1) Participate in intracellular signaling;(2) Regulate angiogenesis;(3) Regulate inflammatory response;(4) Regulate the release of calcium ions; (5) Regulate the movement and migration of target cells; (6) Control of relevant transcription factors and activators, etc [75], [76]. CBD is a GPR55 antagonist that regulates neuronal Ca2+ levels, thus playing an anticonvulsant role [77]. Furthermore, CBD is also a reverse agonist of GPR3, GPR6, and GPR12, which is related to cell survival, proliferation, and neurite growth, as well as neuropathic pain [78]. The effects of CBD on these orphan receptors reveal its therapeutic potentials in diseases such as Alzheimer’s disease, Parkinson’s disease and cancer.
2.2.3. PPARγ receptors
PPARγ receptors are found in adipose tissue and macrophages and are primarily involved in glucose energy metabolism and lipid storage [79]. PPARγ, a ubiquitin E3 ligase, is involved in the regulation of inflammation by inducing the degradation of ubiquitination proteomes of p65, thereby inhibiting the expression of pro-inflammatory genes such as cyclooxygenase (COX2) and some pro-inflammatory mediators such as TNF-α, IL-1β, and IL-6 [80]. CBD is an agonist for PPARγ receptors, through which anti-inflammatory and antioxidant effects can be exerted. It has been found that CBD can activate PPARγ in multiple sclerosis (MS) models and prevent neurodegeneration in AD rat models by reducing pro-inflammatory molecules and stimulating nerve production [81], [82]. In addition, CBD is also reported to significantly induce the transcriptional activity of PPARγ, thereby regulating the occurrence and development of tumors, which lays a foundation for the treatment of tumors with CBD [83].
2.2.4. TRP receptors
TRP channels exist in mammals and are expressed in a variety of body tissues, playing an important role in peripheral neurons [79]. TRP channels are divided into 6 families, namely canonical (TRPC), rekyrin (TRPA), polycystin (TRPP), mucolipin (mucolipin), Rekyrin (TRPA), mucolipin (TRPML), melastatin (TRPM) and vanilloid (TRPV) [84]. CBD acts on transient receptor potential vanillin receptors (TRPV), especially TRPV1, TRPV2, TRPV3, TRPV4, Anka protein 1 receptor subtype (TRPA1), and TRP-8 receptor (TRPM8), and is involved in neurotransmitter release, temperature perception, and pain regulation [85]. CBD mainly interacts with TRPV-1, showing similar effects in vitro to the natural TRPV-1 agonist(capsaicin) [86]. In addition, CBD activates other vanillin receptors, such as TRPV2 and potentially TRPA1, while antagonizing TRPM8 [87]. It has been proposed that CBD activates TRPV2 by binding the small hydrophobic gap between the S5 and S6 helices of adjacent subunits [88]. CBD regulates calcium homeostasis in immune cells and inflammatory cells through TRPV3, a temperature sensor widely expressed in the brain, skin, and tongue [89]. However, CBD was less responsive to TRPV3 than TRPV1 and TRPV2, which may be attributed to differences in the sequence homology of CBD binding sites [84].
2.2.5. 5-HT receptors
Serotonin receptors are widely expressed in multiple brain regions, and specific neurons can express several different serotonin receptors. Serotonin receptors are divided into seven families (5-HT1–7R) with at least 14 different receptor subtypes. They play an important role in physiological regulatory processes, including body temperature regulation, breathing, vomiting, cognitive and emotional regulation, etc [90]. Studies in Wistar rats by Resstel et al. [91] showed that CBD reduces physiological and behavioral responses to restrictive stress by activating 5-HT1 amperometric receptors. Notably, it has been observed that CBD, as an agonist, binds to the 5-HT1A receptor, enhancing its activity and regulating the μ and δ opioid receptors in the cerebral cortex membrane homogenate, thereby reducing anxiety and improving the emotional state of patients [92].
2.2.6. Other receptors
Adenosine A2 ampere-receptors are also G-protein-coupled receptors, for which CBD is an agonist. Some studies have shown that CBD can reduce the level of vascular cell adhesion molecule (VCAM-1) in SJL/J mouse endothelial cells by activating A2 ampere adenosine receptors, which provides a reference for the treatment of multiple sclerosis (MS) [93]. CBD also acts on voltage-gated calcium Cav3. 1/Cav3. 2 and sodium channels Cav3. 3, inhibiting cationic current and reducing the conductance of voltage-dependent anion channel 1 (VDAC1) [94], [95]. In addition, CBD can play a regulatory role in physiological functions through some inflammatory mediators. For example, CBD is able to block the activation of nucleotide-binding oligomerized domain-like receptor (NLR) inflammasome complexes involved in the NF-κB, MAPK, and IFN pro-inflammatory pathways, thereby reducing pro-inflammatory cytokines such as IL-1β and IL-18 [96]. Interestingly, CBD may also interact with various lipid metabolizing enzymes, such as lipoxygenase (LOXs) [97]. Furthermore, many studies have proposed other GI coupled receptors as binding sites for CBD, such as μ and δ opioids, as well as the high-affinity D2 and D3 dopamine receptors [98].
2.3. Distribution and function of CBD receptors in oral cavity
Through the brief description of the receptors of CBD, we have a certain understanding of related pharmacological function. Therefore, summarizing the distribution and function of CBD action receptors in oral activity is the key to revealing CBD-based treatment of oral diseases. Table 2 lists the distribution and function of oral receptors.
Table 2. Tissue distribution and role of CBR in oral and craniofacial tissues.
Receptor name | Distribution in oral tissue cells | Effects | References |
---|---|---|---|
CB1R | Oral mucosa (epithelial cells) | Inhibition of proliferation and differentiation of human epidermal keratinocytes | [99], [100] |
Tongue (epithelial cells) | Feedback on the pathological and physiological state of the tongue | [100] | |
Salivary gland (parietal membrane or adjacent striated duct cells) | Regulation of Salivary Secretion | [60] | |
Dental pulp tissue (nerve fibers and odontoblasts within dental pulp tissue) | It may be involved in regulating tooth pain, promoting dentin formation, and repairing dental pulp tissue | [61], [62] | |
Periodontal tissue (periodontal ligament) | Cell growth and differentiation, inflammatory regulation, and tissue healing | [63] | |
CB2R | Oral mucosa (epithelial cells) | Promote the proliferation and differentiation of human epidermal keratinocytes | [64], [99] |
Tongue taste buds (epithelial cells) | Feedback on the pathological and physiological state of the tongue | [61], [100] | |
Salivary glands (myoepithelial cells around acini, ganglion neurons in secretory ducts) | Regulation of salivary gland secretion | [64], [101] | |
Periodontal tissue (periodontal ligament) | Cell growth and differentiation, inflammatory regulation, and tissue healing | [102], [103] | |
TRPV-1 | Oral mucosa (lamina propria connective tissue) | Physiology and pathophysiology of oral mucosal health and diseases | [100] |
Tongue (epithelial basal layer) | Related to the pathological and physiological state of the tongue | [100], [104] |
CB1R, cannabinoid type 1 receptor; CB2R, cannabinoid type 2 receptor; TRPV-1, transient receptor potential vanillic acid receptor 1.
2.3.1. Oral mucosa
Histologically, the oral mucosa consists of an upper squamous epithelium and a lower connective tissue. The layer of connective tissue contains salivary glands, blood vessels, nerve endings, and immune cells. The cannabinoid receptors, CB1, CB2 and TRPV1, can be identified in the connective tissue of the lamina propria [105]. However, there is limited scientific data on the effects of cannabinoids on oral mucosal tissue receptors [106]. Although there are no clear reports of direct expression of cannabinoid receptors in the oral mucosa, CB1 and CB2 receptors have been found in epithelial cells. It has been reported that the CB2 receptor stimulates the proliferation and differentiation of human epithelial keratinocytes, while the CB1 receptor has the opposite effect [107]. Oral mucosa is at the frontline to contact with cannabis products during consumption, making it the target of oral diseases treatment. The discovery of CB1 and CB2 receptors in oral mucosa is of great significance for the treatment and health maintenance of oral mucosal diseases.
2.3.2. Tongue
The tongue is the most flexible organ in the mouth. CB1 and CB2 receptors are found in the epithelial cells and taste buds of the tongue, and their function appears to be regulated by the physiological and pathological conditions of the tongue. For example, Marincsak et al. [108] found that TRPV1 exists in the basal layer of the lingual epithelium. Theocharis et al. [109]demonstrated that the expression levels of CB1 and CB2 receptors are enhanced in tongue squamous cell carcinoma. And Borsani found that the expression levels of TRPV1 and CB2 in tongue epithelial cells of patients with burning mouth syndrome increased, while that of CB1 decreased [110]. Therefore, in the future, monitoring the expression levels of CB1 and CB2, as well as changes in the ratio of CB1/CB2, may be a means to diagnose and evaluate tongue health.
2.3.3. Pulp tissue
There is little research data on the existence and function of CB1 receptor and CB2 receptor in pulp tissue. Some scholars only detected the expression of CB1 receptor in nerve fibers in pulp tissue at the pulp-dentin boundary [62]. This suggests that cannabinoids may play a role in the mechanisms of toothache and that CB1 receptors may be therapeutic targets for toothache disease.
2.3.4. Periodontal tissue
CB1 and CB2 receptors can be expressed in periodontal tissues, and their distribution varies with periodontal tissue status [64]. In healthy periodontal tissues, the expression level of CB1 receptor in the periodontal ligament (PDL) was significantly higher than that of CB2 receptor [103]. In the presence of infection and inflammation, the expression of CB1 receptor was down-regulated, while that of CB2 receptor was up-regulated in PDL [111]. The differential expression of CB1 and CB2 in PDL may be related to their different cellular functions, especially in regulating periodontal cell migration, proliferation and differentiation. Meanwhile, the changes in expression of CB1 and CB2 are also a direct manifestation of the occurrence of periodontal diseases, and can also be used as a method to monitor the oral periodontal health status in the future.
2.3.5. Salivary gland tissue
In the salivary glands, the distribution of CB1 and CB2 receptors is specific. For example, CB1 receptor is expressed in striatal duct cells, while CB2 receptor is found in acinar cells, especially myoepithelial cells responsible for salivary secretion [61], [112]. In animal experiments, CB1 receptors were found in the major salivary glands of dogs and localized to striate duct cells on or near the parietal membrane, but CB1 receptors were not observed in acinar cells [113]. In addition, Pirino et al. [61]. detected CB2 receptors in ganglion neurons near major secretory ducts in pigs. Interestingly, the presence and distribution of CB1 and CB2 receptors in the salivary glands play a crucial role in saliva secretion, which appears to be regulated by the type and amount of food [114]. Therefore, regulating the expression of CB1 and CB2 receptors may be an effective way to solve oral salivary gland dyssecretion and treat Sjogren’s syndrome.
3. The therapeutic potential of CBD for oral diseases
3.1. Periodontal therapy
Periodontal disease is an inflammatory disease caused by plaque that, if left untreated, can lead to the loss of alveolar bone and eventually the loss of teeth. Fortunately, some scholars have found that the endocannabinoid system can regulate the inflammatory response of periodontal ligament cells and inhibit the progression of inflammation, and also plays an important role in the immunosuppression of porphyromonas gingivalis lipopolysaccharide (LPS) [115]. Therefore, the study of the interaction between CBD and oral endocannabinoid system opens up new ideas for the prevention and treatment of periodontal diseases. Oral biofilm is a complex structure formed by continuous accumulation of more than 600 kinds of bacteria [116]. Dental plaque includes supragingival plaque and subgingival plaque. Supragingival plaques mainly contain aerobic bacteria, while subgingival plaques mainly contain anaerobic bacteria [116]. The accumulation of supragingival plaques eventually leads to the formation of subgingival plaques. Some scholars believe that supragingival dental plaque is a reservoir of periodontal pathogens, which may spread to the subgingival area and cause periodontal disease [117]. Therefore, removal of supragingival and subgingival plaque is the key to controlling and treating periodontal diseases. In clinical work, we take different ways to remove plaque on the tooth surface, but cannot effectively inhibit the bacteria that form dental plaque. As a matter of fact, according to the results of in vitro bacterial culture, there are still active bacteria on the treated tooth surface, which increases the difficulty of the treatment and maintenance of periodontal disease. Fortunately, the study of Vasudevan et al. [118] found that adding CBD to polishing powder can effectively improve the tooth polishing effect, and can inhibit and reduce the recombination ability of bacteria and the formation of new dental plaque, which provides ideas for the control of bacteria and the maintenance of periodontal health after plaque removal. In recent years, with the deepening of research, Blaskovich et al. [30] found that CBD also has a selective inhibitory effect on gram-negative bacteria, and CBD does not produce drug resistance. Therefore, the use of CBD in combination with other anti-gram-negative bacteria or facultative anaerobic drugs may have potential application value in periodontal infection control and periodontal health maintenance. In the future, CBD can also be applied to the treatment of periodontal diseases in the form of drug load sustained release, such as the synthesis of CBD complex drugs similar to minocycline hydrochloride (Palio) and the preparation of CBD drug strips in the form of nanofiber scaffolds.
CBD has also been shown to stimulate calcium ions in transfected HEK-293 cells via TRPV3 and to regulate calcium homeostasis in immune and inflammatory cells primarily through TRP channels [89], thereby regulating cell proliferation and secretion of pro-inflammatory-related cytokine [119]. Petrosino et al. [120] demonstrated that CBD effectively inhibits the production of MCP-2 chemokines and other pro-inflammatory cytokines (such as IL-6, IL-8, and TNF-α) in polymers. It is worth noting that the predictor of pulmonary complications of COVID-19 is the increase of IL-6 level [121]. However, periodontitis will increase the local and systemic IL-6 level, which means that the prevention and treatment of periodontal disease by CBD can reduce the level of IL-6, thereby improving the pulmonary complications caused by COVID-19 and reducing its mortality. In addition, CBD also plays an important role in the prevention and treatment of systemic diseases related to periodontal diseases. For instance, CBD can reduce the incidence of diabetes, regulate the response of diabetes-related inflammation and alleviate the condition of leukemia. Furthermore, CBD’s antagonism to NF-kB prevents the production of interleukin and other inflammatory mediators such as cytokines, chemokines and pro-inflammatory growth factors, thereby alleviating stress responses like inflammation [63]. Among them, CBD exerts anti-inflammatory and antioxidant effects mainly through the receptors related to its action, as shown in Table 3. In animal experiments, Napimoga et al. [122]used 5 mg/kg CBD to treat and treat a rat model of induced periodontitis for 30 days. After morphological analysis of alveolar bone loss, it was found that animals treated with CBD showed regional reduction of bone loss and lower expression of NF-kB. These studies show that CBD has certain potential in controlling periodontal inflammation, removing plaque, inhibiting the further development of periodontitis, and inhibiting the bone resorption of periodontitis.
Table 3. CBD exerts antioxidant and anti-inflammatory effects through related effector receptors.
Receptor name | Mechanisms and roles in regulating inflammation | References |
---|---|---|
CB1R | Activation of CB1R by CBD increases ROS production and pro-inflammatory response | [70], [123] |
CB2R | Activation of CB2R by CBD leads to ROS and TNF- α Reduced levels, reducing oxidative stress and inflammation | [70], [120] |
TRPV1 | CBD binds to TRPV1 and causes desensitization, leading to a “conflicting analgesic activity” similar to capsaicin, reducing the level of oxidative stress to activate TRP | [10], [124] |
TRPV2 | CBD activates TRPV2 and potential subcategories of the Ankarin 1 receptor (TRPA1), while also antagonizing the TRP-8 receptor (TRPM8), playing a role in inflammatory regulation | [86] |
TRPV3 | CBD stimulates calcium ions in HEK-293 cells transfected with TRPV3 and regulates calcium homeostasis in immune and inflammatory cells primarily through TRP channels | [89], [125] |
PPARγ | CBD roles PPAR γ to induce the degradation of p65 ubiquitinated proteasomes involved in the regulation of inflammation, inhibiting the expression of pro-inflammatory genes such as cyclooxygenase (COX2) and some pro-inflammatory mediators | [80], [126] |
GPR55 | CBD is a GPR55 antagonist that can regulate neuronal calcium 2+levels depending on cell excitability, regulate ROS and anti-inflammatory interleukin levels, and thus regulate inflammatory responses | [127], [128] |
5-HT-1 | Activation of 5-HT1 receptor by CBD reduces physiological and behavioral responses to restrictive stress and alleviates inflammatory response | [[92], [129]] |
A2AR | Activation of adenosine A2A receptor by CBD reduces the level of vascular cell adhesion molecule (VCAM-1) in endothelial cells of SJL/J mice and alleviates mitochondrial oxidative stress | [130], [131], [132] |
CB1R, cannabinoid Type 1 Receptor; CB2R, cannabinoid type 2 receptor; GPR55, orphan G protein coupled receptor 55; TRPV, transient receptor potential vanillic acid receptor; TRPV-1, transient potential vanillin receptor type 1; TRPV-2, transient potential vanillin receptor type 2; TRPV-3, transient potential vanillin receptor type 3; ECS, endogenous cannabinoid system; PPAR γ, peroxisome proliferator activated receptor γ; 5-HT1, 5-hydroxytryptamine receptor-1; VCAM-1, vascular cell adhesion molecule 1; COX2, cyclooxygenase 2; TRPA1, ankarin 1 receptor subtype; A2AR, adenosine A2A receptor; ROS, reactive oxygen species; TRP, transient receptor potential.
3.2. Endodontic treatment
It is well known that dental caries is the result of a combination of factors, including bacteria in biofilms and plaque (such as Streptococcus mutans or Lactobacillus), regular intake of sugary foods that lead to acid accumulation, and insufficient cleaning of teeth for a long time, among which bacterial factors are the main factors in the development of dental caries. Studies have shown that CBD can significantly inhibit the bacterial activity in dental plaque and biofilm, and can effectively prevent the formation of oral biofilm and dentin decay, and its antibacterial effect is even the same as chlorhexidine [118]. Streptococcus mutans is a common cariogenic bacteria in oral cavity, which can produce lactic acid through the metabolism of carbohydrates, leading to the occurrence and progression of tooth decay. Aqawi et al. [133] found that CBG can reduce the expression of basic metabolic pathways related to the cariogenic properties of Streptococcus mutans biofilm and various genes involved, and proved that CBG has anti-biofilm activity against Streptococcus mutans, making it a potential drug for the prevention and treatment of dental caries. Therefore, CBD, as one of the main components of cannabinoids, may also have potentials in oral antibacterial as CBG, which needs to be verified by researchers. In addition, promoting the mineralization and repair of dental tissue is the key to the treatment of caries. Petrescu et al. [98]combined CBD with vitamin D3 and found that the addition of CBD can better promote the osteogenic differentiation of mesenchymal stem cells and accelerate the formation and mineralization of calcium nodules. These properties suggest that CBD may have potential therapeutic applicability in preventing and treating dental caries. With the progression of dental caries and the exposure to bacterial infection, pulpitis or even tooth loss may occur [134]. CBD, as a non-psychoactive factor, also has potential advantages in the anti-inflammatory analgesia of pulpitis. CBD can act on the endocannabinoid system in oral cavity, thereby inhibiting the release of inflammatory factors and relieving pain [135]. Meanwhile, CBD can effectively relieve anxiety during pain and improve patients’ sleep. In addition, the regeneration of dentin and the preservation of pulp vitality are crucial problems to be faced in endodontic treatment. For example, studies have found that CB1 receptor and CB2 receptor can be expressed in dental pulp cells and tissues, and activation of CB1 receptor can regulate the entry of extracellular Ca2+ and promote the formation of repaired dentin in odontoblast cells [136]. Qi et al. [137]induced the proliferation and differentiation of human dental pulp cells through CBD, and found that CBD could bind to CB2 receptor, promote osteogenic differentiation of human dental pulp cells through MAPK signaling pathway, and enhance the production of type I and Type III collagen, as shown in Fig. 2. The study suggests that CBD may become a new therapeutic product in dental pulp therapy. More importantly, studies have found that the combined use of CBD and moringa significantly reduces the expression level of inflammatory factors, and promotes the vascular neuralization of dental pulp and periodontal stem cells, indicating that CBD is likely to become a key drug in the treatment of dental pulp regeneration while promoting dentin repair [138].
3.3. Oral mucosa therapy
In recent years, with the acceleration of the pace of life and the increase of related risk exposure factors, the incidence of oral mucosal diseases has been increasing. Various opportunistic pathogens, such as Candida albicans, are present in various parts of the human body including the mouth, vagina and lungs. Some studies have found that CBD can change the structure of fungal biofilms by reducing the thickness of fungal biofilms and the production of extracellular polysaccharide (EPS) [139]. Importantly, it can also inhibit the expression of virulence related genes of bacteria and slow down the damage of bacteria to the body [139]. The pathogenicity of fungi is largely attributed to their ability to adhere and accumulate on various surfaces, and novel anti-fungal strategies focus on developing agents that prevent biofilm formation and eradicate existing biofilms. Therefore, it is of great value to explore CBD as an alternative therapy against fungal infections and oral mucosal diseases. It is worth noting that the use of CBD mouthwash and 0. 2% chlorhexidine can better inhibit the formation of bacterial biofilm, and with the extension of time, there will be no mucosal color change and abnormal taste caused by chlorhexidine [118]. Interestingly, researchers have measured bacterial growth over a 24-hour period using CBD alone or in combination with bacitracin (BAC) [118]. It was found that the combination of 2 μg/mLCBD and 16 μg/mLBAC inhibited the growth of Staphylococcus aureus compared to monotherapy with a single compound. The results showed that CBD could enhance the antibacterial action of BAC [122]. Based on this, CBD can also be used as an auxiliary to enhance component of antibacterial agents in the future. In addition, CBD blocks NT-kB, a regulator of immune and inflammatory responses that is often activated by endotoxins from bacterial lipopolysaccharides, and is also able to reduce the production of inflammatory mediators such as interleukins [140]. This anti-inflammatory and antioxidant properties of CBD may be more effective than classical antioxidants [141]. Taken together, these make CBD possible as a potential therapy for the treatment of mucosal inflammation, because CBD is conducive to epithelialization and promotes the healing of ulcerative lesions in the body.
3.4. Oral tumor therapy
Oral and maxillofacial tumors bring heavy economic burden to patients and society, but also bring great pain to patients. Among them, the two main factors that reduce the quality of life of patients with oral tumors are nausea and vomiting after chemotherapy and cachexia. Researchers face several challenges in fighting oral and maxillofacial tumors, including poor prognosis and intense pain in advanced stages, which require new treatment techniques and drugs. In recent years, studies have found that CBD can interfere with different stages of tumor processes, such as interfering with the invasion and metastasis of tumor cells, promoting the apoptosis of tumor cells, regulating the body’s immune capacity, blocking the formation of blood vessels, and so on [28]. As shown in Table 4, studies on the role of CBD in cancer. The PI3K/AKT/mTOR pathway is one of the basic pathways necessary for physiological protein synthesis and induction of other intracellular pathways, such as the MAPK pathway, which plays an important role in regulating cell survival, proliferation and apoptosis [70]. Some studies have found that CBD can induce apoptosis of leukemia cells by reducing p38-MAPK level [123]. In addition, CBD has also been shown to promote apoptosis in human breast cancer cell lines (T-231D and MDA-MB-1) by inhibiting the expression of carcinogenic and pro-survival cyclins D47 and mTOR, and increasing the expression of PPARγ receptors [120].
Table 4. Research and mechanism of CBD action in tumors
Studies | Tumor types | Tumor cells | Contents and mechanisms | The effect of CBD on tumors |
---|---|---|---|---|
[142] Petrovici et al., 2021 | Malignant melanoma (MeWo), adenocarcinoma (HeLa), hepatocellular carcinoma (HepG2) and osteosarcoma (HOS) | Malignant melanoma (MeWo), adenocarcinoma (HeLa), hepatocellular carcinoma (HepG2) and osteosarcoma (HOS) cells | CBD-enriched hemp oil induces apoptosis in tumor cells by ROS-related mechanisms | The results show that hemp oil enriched in CBD exhibits antioxidant properties in oxidative conditions and has significant anticancer effects on MeWo, HeLa, HepG2 and HOS cells |
[143] Raup-Konsavage et al., 2020 | Colorectal cancer, /glioblastomas, /melanoma | CRC lines (SW480 and HCT116) /GBM cell lines (T98G and U87MG) /melanoma cell lines (1205Lu and A375M) | CBD inhibits the proliferation and activity of SW480 CRC cells, 1205Lu melanoma cells and T98G GBM cells | CBD is not inducing apoptosis, but restricting growth |
[144] Rožanc et al., 2021 | Colon cancer | Caco2 (human colorectal adenocarcinoma cells) | CBD decrease cancer cell viability | CBD decrease cancer cell viability |
[145] Cerretani et al., 2020 | Colorectal cancer | HT-29 Colorectal Adenocarcinoma Cells | CBD appears to induce oxidative stress in HT-29 cells, possibly through ROS production, which causes GSH consumption and inhibits CAT, GR, and GPx activities | Induce Cytotoxicity and Inhibit the Viability of HT-29 Cells |
[146] Sainz-Cort et al., 2020 | Colorectal Cancer | HT-29 Colorectal Adenocarcinoma Cells;SW480 and AGS cells | A low concentration, CBD increases mitochondrial Ca2+ augmenting mitochondrial metabolism and cell growth, but at high concentration, it leads to excessive mitochondrial Ca2+, mitochondrial dysfunction and cell death | CBD (5–20 μg/mL) reduces the viability of cancer cells |
[147] Kargl et al., 2016 | Colon cancer | Colon cancer cell line HCT116 mouse model | GPR55 is involved in the migratory behaviour of colon carcinoma cells and may serve as a pharmacological target for the prevention of metastasis | HCT116 cells showes a significant decrease in adhesion to endothelial cells and in migration after blockade with CBD |
[148] Romano et al., 2014 | Colon cancer | Colon adenocarcinoma cells (i. e. HCT 116 and DLD-1) /mouse model | CBD inhibits the proliferation of colon cancer cells through CB1 and CB2 | CBD reduces cell proliferation in tumoral, but not in healthy, cells |
[149] Jeong et al., 2019 | Colorectal cancer | Human CRC HCT116 and DLD-1 cells/mouse model | CBD induces apoptosis in a Noxa-and-ROS-dependent manner. /CBD-induced noxa regulation leads to apoptosis by causing excessive ROS and ER stress/CBD inhibits tumor growth in vivo by upregulating the expression of noxa, thereby inducing apoptosis | CBD inhibits cell viability and induces apoptosis in human CRC cells |
[150] Sreevalsan et al., 2011 | Prostate and colon cancer | Human LNCaP prostate carcinoma cells/Human SW480 colon carcinoma cell lines | CBD induces phosphatase mRNA expression in LNCaP and SW480cells/CBD-induced apoptosis is phosphatase dependent: the role of CB receptors is ligand dependent | Inhibition of cancer cell proliferation, and induction of apoptosis with CBD |
[151] Zhang et al., 2019 | Gastric cancer | Human gastric cancer SGC-7901 cells | CBD significantly upregulates ataxia telangiectasia-mutates gene (ATM) and p53 protein expression and downregulates p21 protein expression in SGC-7901 cells, which subsequently inhibited the levels of CDK2 and cyclin E, thereby resulting in cell cycle arrest at the G0–G1 phase. In addition, CBD significantly increases Bax expression levels, decreased Bcl-2 expression levels and mitochondrial membrane potential, and then upregulates the levels of cleaved caspase-3 and cleaved caspase-9, thereby inducing apoptosis in SGC-7901 cells. | CBD could induce G0–G1 phase cell cycle arrest and apoptosis by increasing ROS production, leading to the inhibition of SGC-7901 cell proliferation |
[152] Yang et al., 2020 | Pancreatic cancer | Human pancreatic cancer cells, PANC1, CFPAC1, Capan2, SW1990, HPAF11, and MiaPaCa2 /mouse model | CBD and THC exerted their inhibitory effects on PC via a PAK1-dependent pathway, suggesting that CBD and THC suppress Kras activated pathway by targeting PAK1. The suppression of PD-L1 expression by these cannabinoids could enhance the immune checkpoint blockade in PC. | CBD and/or THC not only inhibites PC cells or PSC cells separately, but also suppresses the PSC activity towards stimulation of PC |
[153] Desprez et al., 2021 | The cancer inculding breast, brain, head and neck, and prostate. | Human breast cancer cell lines MDA-MB231 and MDA-MB436 (ATCC), human glioblastoma (GBM) U251 and SF126 (ATCC), human oral squamous cell carcinoma SAS and human salivary gland cancer cell line ACCM (Japanese Collection of Research Bioresources), and human prostate cancer cell lines PC3 and DU145 (ATCC). | CBD inhibits FOXM1 (Forkhead box M1), a transcriptional activator involved in cell proliferation, while simultaneously upregulating GDF15 (growth differentiation factor 15), a cytokine associates with tissue differentiation | CBD leads to inhibition of human cancer cell proliferation, migration, and invasiveness |
[154] Huang et al., 2020 | Human tongue squamous cell carcinoma | The tongue squamous cell carcinoma (SCC-25) | CBD inhibits the proliferation of cancer cells and promotes their apoptosis | CBD significantly increase of the apoptotic cells in a concentration-dependent manner |
[155] Deng et al., | Glioblastoma | Mouse PDGF-GBM Cells and NPCs | CBD decrease cancer cell viability | CBD inhibits the proliferation and migration of cancer cells, induces apoptosis |
[156] Gross et al., 2021 | Prognosis | Canine glioma cell lines SDT3G and J3TBG as well as the human glioma cell lines U87MG and U373MG | Dysregulation of calcium homeostasis and mitochondrial activity. | CBD anti-proliferative, cytotoxic, and induces the formation of intracellular vesicles in glioma cells |
[157] Massi et al., 2004 | Human glioma | U87 and U373 human glioma cell lines | CBD decreases cancer cell viability | CBD inhibits the proliferation and activity of tumor cells |
[158] Solinas et al., 2013 | Malignant gliomas | U87-MG and T98G cell | CBD treatment causes a dose-related down-regulation of ERK and Akt prosurvival signaling pathways in U87-MG and T98G cells and decreases hypoxia inducible factor HIF-1α expression in U87-MG cells. | CBD inhibits proliferation and invasion in U87-MG and T98G glioma cells through a multitarget effect |
[159] Amaral et al., 2021 | Breast cancer | MCF-7aro cells, human epithelial ER breast cancer cells (MCF-7 cell line) | CBD not only exhibites high anti-aromatase activity but also induces up-regulation of ERβ | CBD triggeres autophagy to promote apoptotic cell death |
[160] Elbaz et al., 2015 | Breast cancer | Human TNBC cell line SUM159, murine TNBC cell line 4T1 cells, MDA-MB-231 cells, MVT-1 cell line, MDA-MB-231 and RAW 264. 7 cell lines | CBD inhibits breast cancer growth and metastasis through novel mechanisms by inhibiting EGF/EGFR signaling and modulating the tumor microenvironment. | CBD significantly inhibits epidermal growth factor (EGF) -induced proliferation and chemotaxis of breast cancer cells |
[161] Lukhele et al., 2016 | Cervical cancer | ME-180 and SiHa | CBD induces the increase of subG0/G1 and the apoptosis of Annexin V, the increase of Caspase 3/7 and the decrease of ATP level, which promotes the apoptosis of cancer cells | CBD inhibits the proliferation and activity of tumor cells |
[162] Milian et al., 2020 | Non-small cell lung cancer | A549, H460 and H1792 human lung cancer cells | CBD inhibites the proliferation and expression of EGFR in the lung cancer cells studied. Finally, the THC/CBD combination restores the epithelial phenotype in vitro | CBD inhibits the proliferation and expression of EGFR in lung cancer cells |
[163] Maor et al., 2012 | Kaposi sarcoma | Primary HMVECs | CBD inhibites the expression of KSHV viral G protein–coupled receptor (vGPCR), its agonist, the chemokine growth-regulated protein α (GRO-α), vascular endothelial growth factor receptor 3 (VEGFR-3), and the VEGFR-3 ligand, vascular endothelial growth factor C (VEGF-C). | CBD inhibits growth and induces programmed cell death in kaposi sarcoma–associated herpesvirus-infected endothelium |
ATP, adenosine triphosphate;HMVECs, human dermal microvascular endothelial cells;EGF/EGFR, epidermal growth factor receptor;GRO-α, growth-regulated protein α;VEGFR-3, vascular endothelial growth factor receptor 3;vGPCR, viral G protein–coupled receptor;VEGF-C, vascular endothelial growth factor CATM, ataxia telangiectasia-mutates gene.
The antitumor activity of CBD is mainly mediated by plasma membrane-associated receptors, such as GPR55 and TRPV1/2. Relevant studies have found that GPR55 is a key factor in tumor progression, and CBD as a GPR55 antagonist can counteract its role in promoting tumor cell growth, thereby inhibiting tumor progression [164]. A recent study showed that CBD can induce autophagy in glioma stem cells in a TRPV2-dependent manner, and this pathway is regulated by the AKT/mTOR network, in which Beclin-1 protein plays a central role [165]. In addition, the sensitivity of tumor cells to chemotherapy drugs is induced by the action of CBD on TRPV2 [166]. CBD can also be used as a novel GPR12 reverse agonist to inhibit cAMP accumulation stimulated by structurally active GPR12 and regulate the adhesion of metastatic tumor cells [167]. Tumor progression is accompanied by the generation of a large number of microvessels, and the oral cavity is an environment with rich blood circulation, and tumors are often accompanied by rapid metastasis and progression. In recent years, studies have found that CBD has a strong anti-angiogenesis ability in vitro, which can interfere with the protein expression of various regulators involved in the angiogenesis process. As studies have shown, CBD can down-regulate the expression of VEGF, inhibit hypoxia-inducible factor-1 α in U87-MG glioma cells, and inhibit cell angiogenesis under hypoxia environment [158]. On this basis, if CBD drugs that act on GPR12 and down-regulate the angiogenesis of cancer cells can be developed, certain breakthroughs may be made in the treatment of oral cancer invasion. In addition, the activation of the immune system plays an important role in the suppression of tumor cells, and a clinical study found that CBD can stimulate the immune system and enhance the sensitivity of tumor cells to killer cells [168]. More importantly, advanced oral and maxillofacial tumors are often accompanied by severe chronic pain. The use of CBD can better control pain, relieve anxiety and help patients sleep, and patients will not develop drug dependence. Allosteric regulation plays an important role in the signal transduction mechanisms of many proteins, which favor proteins that enhance (i. e., positive allosteric regulators) or reduce (i. e., negative allosteric regulators) activity [169]. At present, it has been reported that CBD can play a certain allosteric regulatory role through at least three plasma membrane targets (GPR55, CB1 and TRPV1), which lays a foundation for CBD to develop drugs for the treatment of oral tumors. In terms of products, at present, epididymol (containing CBD) sold by GW Pharmaceuticals is prescribed as an adjuvant for the treatment of glioma [170].
3.5. Temporomandibular joint treatment
In recent years, the incidence age of oral temporomandibular joint diseases has gradually shown a trend of younger. Factors such as bad oral habits, life and mental pressure have become the important reasons for the occurrence of temporomandibular joint diseases, among which temporomandibular joint disorders (TMD) are the most common. TMD is often associated with restricted mouth opening, swelling, and pain. A study in 2012 found that CBD is an excellent blocker, blocking nerve conduction [171]. In addition, Hammell et al. [172] administered CBD to a rat model of arthritis and found that CBD significantly reduced joint swelling, spontaneous pain, immune cell infiltration, and synovial thickening in a dose-dependent manner. This means that CBD can be used to treat TMD. In mammals, TRPV1 immunoreactivity is located in the injurious primary afferent nerve that innervates the knee joint. After inflammation, TRPV1 expression is not only increased in the primary afferent nerve, but is also detected in synovial cells, which secrete lubrication into the synovial space and function as local immune cells [173]. Therefore, TRPV1 acts as one of CBD’s receptors, and CBD desensitization to TRPV1 may interrupt further progression of this cycle [174], [175]. In conclusion, CBD’s special pharmacological effect may bring good news for the treatment of TMD patients. In addition, CBD has good antibacterial and promoting the migration and osteogenic differentiation of mesenchymal stem cells (MSCs), which will also be a major research highlight in promoting the healing and repair of articular cartilage in the future. Of course, these still need to be excavated and explored by researchers in the future.
3.6. Treatment of maxillofacial bone tissue defect
Bone defects caused by oral and maxillofacial trauma, tumor, radioactive osteonecrosis, jaw osteomyelitis and congenital defects have a great impact on patients’ psychology and physiology [176]. The regeneration and repair of oral and maxillofacial region has always been the focus and difficulty in the field of stomatology. The presence of cannabinoid receptors in bone has brought new ideas for the regeneration and repair of bone defects. CB1 and CB2 receptors are expressed in bone and regulate bone homeostasis in humans. The expression level of CB1 receptor in bone cells is very low, while the expression level of CB1 receptor increases with age, and the upregulation of CB1 receptor expression can protect against age-related bone loss and osteoporosis [177]. CB2 receptor polymorphism is associated with osteoporosis and bone strength. CB2 receptor, as the main receptor of CBD, plays an important role in bone tissue regeneration and repair (such as stimulating cell proliferation and activity). Some studies have found that CBD stimulates bone formation and inhibits bone absorption by acting on CB2 receptors, activating CB2 receptors [178]. These effects may lead to new bone formation and improved biomechanical properties of bone tissue, making CBD a suitable therapeutic adjuvant for bone loss caused by oral and maxillofacial surgery or trauma. For example, in our current study, we extracted human jaw bone marrow mesenchymal stem cells for culture, proving that a certain concentration of CBD can promote the proliferation and biomineralization of human jaw bone marrow mesenchymal stem cells. Furthermore, human jawbone marrow mesenchymal stem cells and CBD were loaded together on the electrospinning fiber scaffold to construct an extracellular matrix (ECM) space supporting cell growth, and to study its influence on the repair and healing of bone defects, providing a basis for the future clinical application of CBD, as shown in Fig. 3.
In animal experiments, CBD administration has been shown to reduce subcutaneous cancellous bone loss in rats with severe spinal cord injury [179]. In oral studies, Li et al. [180] studied the effects of different concentrations of CBD on the osteogenic differentiation of human periodontal stem cells, and found that a certain concentration of CBD can effectively promote the proliferation and osteogenic differentiation of human periodontal stem cells, and proposed that CBD may down-regulate the main inhibitory factor of Wnt/β-catenin pathway, GSK-3β. The Wnt/β-catenin pathway is activated, which may be related to the anti-inflammatory and antioxidant stress properties of cannabidiol. In terms of scaffold materials, Kamali et al. [181] created a gelatin/nano-hydroxyapatite (G/nHAp) scaffold that delivers CBD-loaded poly (lactate-co-glycolic acid) (PLGA) microspheres to critical size radial bone defects in a rat model. This study found that the incorporation of CBD significantly increased the migration of MSCs and improved the healing of bone defects, demonstrating that the combined use of CBD plays a key role in promoting the migration of MSCs and the process of bone regeneration. It is well known that bone reconstruction often relies on replacement grafts, with disadvantages including limited available bone substitutes, complications, inflammatory responses, immune rejection, and limited endogenous bone regeneration. Among them, chronic inflammation of bone tissue usually leads to bone defects and harm to tissue repair and regeneration. Li et al. [182] stimulated bone marrow mesenchymal stem cells (BMCs) with lipolysaccharide (LPS) to induce an inflammatory microenvironment, and found that CBD intervention down-regulated the mRNA expression of inflammatory cytokines in LPS-treated BMSCs and promoted cell proliferation, and also reversed the downregulation trend of protein and mRNA levels of osteogenic markers induced by LPS treatment. In conclusion, CBD has potential application potential in oral and maxillofacial defect reconstruction. Table 5 shows research and application of CBD in regeneration of oral and craniofacial tissues in recent years.
Table 5. Recent research and application of CBD in the regeneration of oral and craniofacial tissues.
Studies | Cells | Materials | Research contents | Applications |
---|---|---|---|---|
[183] Sangiovann et al., 2019 | HaCaT and HDF | – | CBD inhibit in vitro mediators of skin inflammation and wound injury | Wound dressing Inflammation treatment |
[181] Kamali et al., 2019 | MSCs | CBD-PLGA-G/nHAp | Microspheres loaded with cannabidiol for bone defect regeneration | Tissue engineering |
[184] Yu et al., 2023 | DPSC | – | The effect of CBD on DPSCs proliferation, migration, and osteogenic/odontogenic differentiation | Dental pulp treatment Bone tissue engineering |
[185] Soundara et al., 2017 | hGMSC | – | The effect of CBD on the expression of the genes related to the neural differentiation of hGMSCs | Treatment of neurodegenerative diseases |
[186] Zhang et al., 2022 | NSCs | CMC/CS/CBD | Cannabidiol-loaded hydrogels (CMC/CS/CBD) for the treatment of spinal cord injuries | Spinal cord injury repair |
[187] Zheng et al., 2021 | HUVEC and RAW246. 7 cells | CBD/Alg@Zn | An alginate-based hydrogel loaded with cannabidiol for wound healing | Wound dressing |
[188] Kang et al., 2020 | U2OS and MG-63 | – | Cannabidiol Induces Osteoblast Differentiation via Angiopoietin 1 and p38 MAPK | Bone tissue engineering |
[182] Li et al., 2022 | BMSCs | – | Mechanism of cannabidiol on osteogenic differentiation of bone marrow stem cells in inflammatory state | Inflammation treatment Bone tissue engineering |
[189] Qi et al., 2022 | MC3T3-E1 cells, HUVECs and RAW 264. 7 cells | SA@Cu/CBD hydrogels | Effect of Cannabinol loaded Copper Alginate Hydrogel on Osteogenesis | Bone tissue engineering |
[190] Monou et al., 2022 | HaCaT cell line | SA/CBD-NPs films | The effect of 3D printed alginate film loaded with CBD on wound healing | Wound dressing |
HaCaT, human immortalized epidermal cell; HDF, human dermal fibroblasts; MSCs, mesenchymal stem cells; DPSC, dental pulp stem cells; HGMSC, human gingival mesenchymal stem cells; NSCs, neural stem cells; HUVEC, human umbilical vein endothelial cells; BMSCs, bone marrow mesenchymal stem cells; CBD, cannabinoid; SA, silk fibroin; CS, chitosan; PLGA, polylactic acid hydroxyacetic acid copolymer; CMC, carboxymethyl cellulose.
3.7. Treatment of other oral diseases
In addition to this, CBD also plays an important role in other aspects of the mouth. Angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2) are the key viral channels of oral, lung and intestinal epithelial cells and important pathways of SARS-CoV2 invasion [191]. Studies have reported that in the presence of oral ECS, CBD can down-regulate the expression of oral ACE2 and TMPRSS2 [192]. Therefore, the use of CBD-containing products, such as mouthwashes, to down-regulate ACE2 and TMPRSS2 may serve as a preventive strategy for COVID-19 infection. In addition, CBD, as a drug for the treatment of epilepsy, plays an important role in regulating mental state, relieving mental stress and promoting sleep in patients, and the use of CBD may be of great value in the treatment of oral related psychiatric diseases, such as burning mouth syndrome, trigeminal neuralgia and hysteria. It is worth noting that CBD, with its good antibacterial and bone-promoting ability, may also have certain therapeutic potential in the future in promoting implant bone adhesion and preventing and treating implant mucosal and peripheral inflammation.
4. The administration route of CBD for oral disease treatment
This paper summarized the potential of CBD in the treatment of oral diseases, and discussed the research status of CBD in the field of oral diseases. However, there is still a long way to go for CBD to be truly applied in oral clinic in the future, and the analysis and selection of administration routes for CBD oral disease treatment are also important issues. Therefore, this part summarized the administration routes of oral, intravenous, sublingual, transdermal and nasal administration (as shown in Table 6) and preliminarily discussed the possible administration routes of CBD while treating oral diseases in the future, hoping to provide some reference for its clinical application in oral medicine.
Table 6. The advantages and limitations of different routes of administration.
Route of administration | Advantages | Limitations | References |
---|---|---|---|
Oral administration | Easy to administer, easy to use, self-managing and non-invasive. | High-fat drugs are not easily absorbed; drugs are affected by digestive tract enzymes; it is difficult for people with difficulty swallowing or diseases of the mouth, pharynx, and esophagus to choose oral administration. | [193], [194], [195], [196], [197] |
Intravenous administration | Can be used in acute indications requiring rapid, high systemic concentrations. | Unsuitable for patients who receive frequent medication and is invasive. | [198], [199], [200], [201] |
Sublingual administration | Non-invasive administration methods that avoid first-pass metabolism; safe and effective. | The scope of application is limited, and it is more suitable for oral local ulcer diseases. | [202], [203], [204], [205] |
Nasal administration | Non-invasive, can quickly achieve passive diffusion of drugs, avoid the influence of gastrointestinal enzymes, alternative administration methods with abnormal swallowing function. | The dosage is limited, making it unsuitable for high-dose drug therapy; the molecular weight of the drug is limited; the drug utilization rate is affected by nasal mucus, cilia and respiratory conditions. | [193], [206], [207], [208], [209], [210], [211] |
Pulmonary administration | Ideal for treating respiratory diseases. | Drug type, drug molecular weight, and wettability are limited. | [193], [199], [212], [213] |
Transdermal administration | Non-invasive, avoids first-pass metabolism, and maintains local subcutaneous drug concentrations for a long time. | It is not the first choice for the treatment of acute diseases; treatment is concentrated on local treatment; drug absorption is incomplete. | [[207], [214], [215], [216]] |
Vaginal administration | Avoiding the first-pass effect; effective in the treatment of reproductive system diseases; reducing gastrointestinal reactions. | Requires strong adherence; applies only to low-molecular-weight drugs; drug availability is susceptible to motion and enzymes. | [217], [218], [219], [220], [221] |
Rectal administration | Avoiding the first-pass effect; suitable for gastrointestinal diseases (cancer, ulcers, etc.) | Strong compliance is required; the method of administration is difficult; it is easy to cause discomfort. | [193], [222], [223] |
Ocular administration | Non-invasive; very suitable for treating local eye diseases. | Drug retention in the anterior pocket of the cornea; strong adherence is required; drug absorption is affected by tears and eye movements. | [224], [225], [226], [227], [228] |
Ear administration | Local ear disease treatment; Avoiding severe side effects of oral, intravenous, and intramuscular therapy for inner ear infections; Invasive or non-invasive administration. | Strong compliance is required; the blood-inner ear barrier leads to poor drug permeability; higher doses of drugs are required and the probability of toxicity is high; side effects such as hearing impairment are associated. | [229], [230], [231], [232] |
4.1. Oral administration
For most therapeutic molecules, the oral route is the most common and patient preferred route of administration. Because its main advantages include convenience, ease of use, self-management and non-invasiveness [193]. Currently, a variety of oral CBD preparations are available, such as oil drops and capsule oils [205]. Oral administration usually takes place through the mouth, pharynx, esophagus, stomach, duodenum, small intestine, and large intestine. Among them, the gut plays a key role in the absorption of drug molecules. However, the physicochemical properties of drug molecules, such as water solubility, stability, lipophilicity, fraction size and crystallinity, affect the degree of drug absorption. Therefore, the high lipophilicity of CBD may precipitate directly in the gastrointestinal tract, leading to CBD malabsorption and low drug availability [195]. In animal models of mice, dogs, horses, and dairy calves, there was a delay ranging from 2 to 7 hours in reaching a predetermined peak plasma concentration of CBD after oral administration [194], [196], [205], [213], [233], [234]. The low absorption of CBD in the blood limits the therapeutic effectiveness of acute central neurological diseases of the brain. This delay in the treatment of sudden oral and maxillofacial cancer pain means that early prophylactic administration may be necessary. Some scholars have proposed that the absorption of CBD can be improved by taking it with a high-fat diet [235]. In other areas, after taking CBD orally, the researchers detected CBD in the brains of rats and mice, as well as in synovial fluid and joint tissue (articular cartilage and subpatellar fat pads) in horses and guinea pigs [236], [237]. The location of CBD after oral administration, as well as the distribution of its action receptors as described above, support CBD’s potential use in central nervous system diseases and musculoskeletal pain. In particular, it supports the treatment of joint tissue areas by oral administration, which makes it possible to treat oral temporomandibular joint diseases.
4.2. Sublingual administration
The tongue is the most flexible organ in the mouth, and its abundant taste buds and blood vessels play a key role in it. The mucosa under the tongue is very thin and accompanied by a large number of capillaries, which provides the basis for systemic treatment with drugs. Therefore, sublingual administration is one of the important ways to treat local or systemic diseases [202]. Vitetta et al. [238] found that CBD was rapidly absorbed within 1 hour when ingested sublingual, but bioavailability was not reported. So sublingual administration is feasible for the treatment of local or systemic acute symptoms, and can be used to relieve the pain of oral mucosal diseases, oral muscle spasms, oral area infections, and tongue cancer symptoms. For example, some researchers have classified CBD and THC as 1;1 Mix to make an oral mucosal spray to relieve moderate to severe multiple sclerosis spasms [202]. However, the inevitable entry of CBD into the intestinal system during sublingual ingestion means that the ultimate pharmacological pathway of CBD is still controversial. It is necessary to adopt a standardized and standardized way to conduct research on the pharmacological pathway of CBD in order to determine the best route of CBD administration. Secondly, sublingual ingestion of CBD will be affected by oral saliva and swallowing. In order to ensure the continuity of sublingual CBD uptake and drug effectiveness, it is necessary to extend the retention time of CBD mucosa in the form of mucosal adhesives [238]. This method can be used to treat local oral ulcers and associated mucosal lesions. Secondly, the discovery of oral cannabinoid receptors also makes it possible for sublingual CBD to treat oral tongue diseases (such as burning mouth syndrome and fungal glossitis, etc.) and salivary gland diseases (such as Schergren syndrome, salivary gland inflammation and salivary gland secretion abnormalities, etc.).
4.3. Intravenous administration
Intravenous injection is a common drug delivery method in clinical practice. Intravenous administration can quickly reach the therapeutic concentration of the drug throughout the body, and can effectively maintain the therapeutic effect. And it can quickly make the drug directly into the systemic circulation, bypassing the first pass of metabolism, and has positive therapeutic significance for patients with shock, pain or acute infection [203]. For example, Xu et al. [198] injected 10 mg CBD into each kg of mice intravenously and found that the drug concentration in the body quickly reached 18 times that of oral administration. Similarly, Meyer et al. [199] demonstrated that intravenous CBD was found to reach drug action concentrations in humans within 10 minutes. However, CBD is a highly lipophilic drug with low solubility and is difficult to administer intravenously by proportionally mixing it with saline. Therefore, this means that CBD can only be administered intravenously if it is soluble in lipids (such as soybean oil and fat emulsions, etc.), organic solvents (anhydrous ethanol) and polymers (polyethylene glycol) [199], [200], [201]. These solvents will have more or less toxic effects on the body, which is obviously difficult to meet the clinical principles of treatment, and most of the current experiments only stay in the animal experiment research stage. In addition, in terms of the clearance rate of drugs in vivo, Paudel et al. [200] conducted relevant studies on rats, and the results showed that the CBD plasma concentration decreased from 3596 ng/mL to 18. 9 ng/mL and 9 ng/mL respectively in 1 h and 2 h. This means that in order to maintain the therapeutic concentration of CBD in the body for a certain time in the future, it has to be repeatedly administered on time and quantitatively, which is obviously not in line with the non-invasive and convenient clinical treatment. Therefore, intravenous administration is difficult to choose for the treatment of oral diseases, and other ways of administration for oral diseases may be more routine in the future.
4.4. Transdermal administration
The skin is the body’s largest organ and consists of three layers: the epidermis, dermis, and subcutaneous tissue. The skin not only plays an important role in protecting the body and maintaining physiological functions, but also plays a key role in drug therapy. Local skin administration can be defined as the local treatment of skin diseases, while transdermal administration is the use of the skin as the site of local and systemic administration [239]. Transdermal administration has two main advantages over oral administration: low patient compliance requirements and high cost effectiveness; This is followed by a lower first-pass metabolic rate and the ability to terminate the drug delivery system at any time [240]. According to relevant studies, transdermal administration of CBD drugs has a good therapeutic effect in the persistent treatment of rat models with chronic inflammation, such as arthritis [193]. Some researchers also use CBD in band-Aids, creams and gels for wound treatment. For example, Lodzki et al. [215], after applying 3%w/w CBD patch on the skin of mice, found a large amount of CBD accumulation in the skin of mice. Interestingly, after transdermal, CBD was also detected in other locations, such as the buttock skin, abdominal skin, muscle, liver, and pancreas of mice. Transdermal delivery gives the advantage of storing drugs locally in the skin and maintaining drug concentrations over a period of time. For example, Paudel et al. [200] found the transdermal reservoir effect of CBD in the skin of guinea pigs. Steady-state CBD levels of 6. 3 ng/mL were reached 15. 5 hours after gel application and continued for 48 hours [200]. This phenomenon is very useful in the treatment of local skin lesions, infections and tumors. However, transdermal administration cannot enter the systemic circulation as quickly as intravenous administration to exert systemic effects. First, the drug needs to pass through multiple layers of tissue, and when it passes through the lipophilic stratum corneum, it accumulates and is difficult to penetrate deep. Second, it takes time to reach and cross the blood-brain barrier, and the clearance of drugs as described above after entering the systemic circulation is also very high. Therefore, the treatment of some oral and maxillofacial chronic local diseases is more suitable, systemic and acute symptoms of disease treatment is often limited.
4.5. Intranasal administration
Thousands of years ago, ancient people had records of intranasal administration of drugs to treat diseases. The earliest record of nasal drug delivery dates from the 16th century BC, with ancient Egyptians inhaling steam from the heated herb Hyoscyamus niger to ease breathing difficulties [241]. Some drugs for nasal delivery are well established and have been in use for decades. Nasal administration is non-invasive and can be self-administered by the patient. Major challenges of nasal administration include controlling particle/droplet size, the small amount of mucosal fluid available for drug dissolution, removal of undissolved particles, the effects of disease on respiratory anatomy and physiology, and local metabolic enzymes [193], [242]. However, compared with oral administration, the enzyme activity of the nasal cavity is relatively lower than that of the gastrointestinal tract, which can avoid drug degradation caused by the harsh environment of the gastrointestinal tract (such as stomach acidity, digestive enzymes, food contents). In addition, it has a well-vascularized and thin mucous membrane that allows passive diffusion into the blood and enhances drug absorption [206], [207]. Therefore, intranasal administration is ideal for local treatments such as allergic rhinitis. Paudel et al. [200] developed various nasal preparations, and found in the rat model study that CBD preparations were absorbed quickly in the nasal cavity (t Max ≤10 min), avoiding the degradation of CBD in the gastrointestinal tract. However, the current research only stays in the animal research stage, and future human clinical studies still need to be carried out, of course, which requires a large number of animal experiments in the early stage to determine its safety and effectiveness. In addition, the nasal cavity can also be used for systemic administration, depending on the nasal mucosa and the large number of capillaries in the lungs. However, this requires the molecular size of inhaled drugs to be limited, and generally (>5μm) drug particles have difficulty entering the lungs [193]. Therefore, nasal treatments in 5–10μm drugs are common in nasal products [193]. The nasal sense of smell and the trigeminal nerve pathway are connected to the brain, and perhaps in the future, the nasal administration of CBD is a potential treatment for central nerve diseases of the brain (such as trigeminal neuralgia and Bell’s palsy).
4.6. Other routes of administration
In addition to the routes described above, a number of other routes may also be used for systemic CBD administration, such as pulmonary, eye, ear, and recto-vaginal administration. Pulmonary administration is ideal for the treatment of respiratory diseases because it achieves high drug concentrations directly and quickly at the target site and can be administered throughout the body [193]. The ancient Chinese have records of using opium to treat severe coughs, diarrhea, and pain [193]. However, although smoking marijuana can get molecules into the lungs and brain quickly, the toxic products produced are far more powerful than the drug. Certainly this is not in accordance with the law and clinical treatment basis. In addition, formulation strategies using CBD dry powder need to overcome the challenges of poor wettability and low solubility, both of which are due to the high lipophilicity of the drug. Therefore, aerodynamic small particles should be generated for deep lung deposition to facilitate whole-body delivery of CBD [243]. When drugs are administered through the eye, the first thing that comes to mind is the treatment of glaucoma. The ocular route is mainly used for local treatment, but systemic absorption of the eye is also possible due to the elevation of the conjunctival vessels [236]. CBD, which is usually highly lipophilic, can be absorbed into the aqueous humor through the cornea and then enter the systemic circulation to play a therapeutic role [244]. At present, there are no studies on the administration of CBD in the eye, but Chiang et al. [226] studied THC administration in the eye of rabbits. Owing to the chemical similarity of CBD and THC, it is possible to systematically deliver CBD through the eye, but this is something that needs to be studied and validated. In patients where oral and inhalation administration is not possible, systemic administration in the rectum or vagina may also be attempted in the form of suppositories. However, it is difficult to achieve drug concentration in this way. For example, some scholars tried to study the PK curve of 100 mg CBD suppository in healthy dogs, and the results showed that the plasma CBD level was below the quantitative limit, so the data could not be analyzed [208]. Perhaps in the future CBD could be attempted to be administered through the rectum like diazepam and levetiracetam for rapid and effective seizure treatment, but this needs to be studied. Vaginal administration of CBD has not yet been reported, but oral Bethell’s disease is often accompanied by vaginal ulcers, and vaginal CBD suppository treatment may be a major research highlight. In addition, CBD drug injection therapy in local areas is also an important way of CBD administration in the future, such as direct injection therapy for TMD joint cavity, inflammatory space of myofascial and pus cavity.
5. Current challenges and future prospects
5.1. Challenges and possible solutions
Some drawbacks and challenges may limit the research and application of CBD. First, although there is evidence that CBD can be used to treat oral diseases, the scientific evidence for its use in dentistry is limited. The application of CBD in the treatment of oral diseases has almost no scientific literature and patent records [245]. Therefore, in order for CBD to be truly applied to all aspects of the dental medicine field, further rigorous, standard and sound scientific studies are needed to confirm their safety, tolerability, efficacy, optimal dosage and optimal delivery system in the treatment of dental diseases. Including from CBD extraction, purity control and the unification of the way of administration, in vitro and in vivo studies in a strictly standardized manner. In addition, for its safety and rationality, researchers are encouraged to try to start with the development of dental products such as toothpaste, mouthwash and floss for oral health maintenance. Currently, most studies have been conducted in animal models (mice, rats, and rabbits), which means that these results may differ histologically and pathologically from those in humans, which can only be instructive [116]. Therefore, it is necessary to conduct similar studies in large animals such as primates to further verify the safety and effectiveness of CBD. Secondly, most of the research on CBD in tumors focuses on tumors of the nervous system, digestive system and respiratory system, while the research on oral tumors is very urgent [246]. At present, there are only a few studies on tongue squamous cell carcinoma [247] and salivary gland cell carcinoma [118] in oral tumor research. It is worth noting that most clinically available anticancer drugs are non-selective, coupled with the complexity of the tumor itself and the associated tumor microenvironment, as well as the unknown side effects of CBD and the lack of long-term experimental studies, which limit its clinical application in the treatment of tumors. In conclusion, there remain numerous obstacles and challenges in the utilization of CBD for the treatment of oral diseases. For example, the anti-inflammatory effects of CBD in the treatment of periodontitis are intricately linked with immunosuppression. Long-term immunosuppression can disrupt the body’s immune regulatory mechanisms, creating imbalances. Moreover, the distribution of oral endocannabinoid systems throughout different regions of the mouth makes it challenging to ensure that CBD provides a precise therapeutic benefit in targeted tissue. Consequently, from a comprehensive perspective, further research on the optimal administration mode of CBD is warranted to promote precision treatment. Furthermore, there has been a lack of randomized clinical trials with an intervention placebo control, posing a significant challenge for the reliable evaluation of the efficacy of CBD in the management of oral inflammatory diseases [248]. It is worth noting that the anti-inflammatory activity of CBD in the oral cavity depends not only on its effect on periodontal tissue, but also on its interaction with oral microbiota, especially surrounding pathogens. This means that the specific mechanism of CBD in the treatment of oral inflammatory diseases and oral mucosal infectious diseases still needs a lot of research to confirm, and it is also convenient for rational clinical application in the future. In addition, the research on CBD in tooth pulp only stays in the in vitro cell experiment, and the future in vivo experiment is still the mining point of research. Of course, relevant studies have shown that CBD has certain pharmacological effects in anti-inflammatory and analgesic aspects, but its clinical treatment in the temporomandibular joint is still blank and remains in the animal experimental stage. But overall the future is promising, with the Drug Enforcement Administration reclassifying CBD as a drug with low abuse potential, expanding CBD’s research potential in the treatment of oral diseases. At the same time, a large number of studies have shown that the distribution and action of receptors acted by CBD in the mouth make CBD very likely to solve many problems in the treatment of oral diseases. However, more studies on the mechanism of CBD and its receptors are also needed in the future to further lay the foundation for the precision treatment of CBD.
The fact that CBD is allowed for clinical use and deregulated does not assure patients of the quality, effective dose, purity and absence of chemical or microbial contamination of the product itself. It means that CBD pharmaceutical products must be mandatory, like other drugs, need to ensure safety, effectiveness and quality standards of product licensing to protect public health, and all products that have been marketed without permission are illegal and must be withdrawn [21]. It is worth noting that CBD has been approved for use in patients in many countries, and there is still a lack of clinically relevant research and evidence-based medicine in oral medicine, which means that the available evidence is of low quality and prone to the risk of bias [249]. In addition, although we have discussed the possible administration routes of CBD, this is actually achieved based on a large number of animal experimental studies and in-depth analysis of the safety, effectiveness and rationality of various administration routes, and there is a long way to go in the future. Including tracking the long-term clinical efficacy and side effects of CBD, the frequency and extent of adverse reactions may also increase with the increase of dose. Of course, through the summary of the drug administration route, it provides a research idea and reference value for the future application of CBD in the treatment of oral diseases. For example, we found that CBD has high lipophilic properties, and we can carry out drug loading applications in the form of nanocarriers [193]. Among them, liposome is an effective nanocarrier composed of phospholipid bilayer, which can encapsulate hydrophilic and lipophilic drugs, and can provide a good choice for drug delivery of CBD. In addition, the solubility of CBD can be improved through various formulations, such as the use of cyclodextrins [250], [251], [252], mesoporous silica [253], polymers [200], [254], self-emulsifying drug delivery systems [255], [256], [257], [258], and other nanomaterials [259], [260], [261]. By increasing the solubility of CBD through these formulations, oral bioavailability can be improved. At the same time, the different routes of administration indicate the therapeutic range and action characteristics of the drug. According to the type and degree of oral diseases, comprehensive treatment with different or multiple drug administration routes can be adopted. For example, some oral mucosal diseases can be treated effectively and safely simply by gargling and sublingual ingestion of drugs. However, for oral and maxillofacial tumors, we have to take a variety of administration routes such as oral, intravenous and transdermal administration to ensure the concentration and persistence of the drug. In addition, oral and maxillofacial symptoms involved in central nervous system disorders often require continuous drug treatment to maintain their therapeutic effects and prevent recurrence, which can be achieved through intranasal or inhalation administration, as both of these methods allow for non-invasive self-administration [193]. Transdermal administration provides a consistent and stable drug concentration that reduces the frequency of administration and is ideal for the treatment of local oral mucosal lesions, tumors, and infections. In other ways, inhalation of CBD can achieve faster and higher drug absorption than transdermal routes because of the large surface area of the respiratory epithelium. This can be used to treat acute central nervous system symptoms, such as pain and anxiety attacks. Nasal administration can act on the central nervous system quickly, and it also provides a way to treat oral and maxillofacial trigeminal neuralgia. In short, to treat any disease quickly and effectively in order to achieve effective disease management, it is necessary to find an optimal route of CBD administration. But this process obviously has a long way to go and is full of unknowns and challenges. In conclusion, the clinical application of CBD will not be achieved overnight, and it is hoped that these challenges will be addressed through multidisciplinary collaboration among clinicians, pharmacological researchers and biomedical engineers.
5.2. Future prospects
So far, CBD has very few research and patents related to dentistry, and it has a lot of room for dental product development and technology application. First of all, the distribution and existence of cannabinoids and other receptors in the mouth laid the research foundation for CBD treatment of oral diseases. Secondly, a large number of studies have shown that CBD has rich and significant pharmacological effects, such as anti-inflammatory, antioxidant, antibacterial, anti-tumor and neuroprotective aspects [262]. This makes it have positive therapeutic potential in the treatment of oral diseases. In the future, after fully verifying the safety and effectiveness of CBD and establishing a scientific clinical treatment system and program, CBD will bring good news to the treatment of human oral diseases.
The multidisciplinary development has provided a variety of options for the study and application of CBD. Among them, the development of tissue engineering in recent years has provided a reference for CBD loading, release, precision therapy, collaborative therapy and intelligent application. In the future, CBD can be applied in the diagnosis and treatment of oral diseases through tissue engineering technology, such as the research and development of pulp cap agents, regenerative pulp scaffolds, 3D collagen matrix, temporomandibular joint lubrication fluid and jaw defect reconstruction scaffolds. It is even possible to prepare some biomimetic and intelligent 3D nanoscaffolds with 3D printed CBD loads. These scaffolds can be solid, porous, banded, core-shell, hollow, beaded and multi-channel forms to meet the release of CBD in different scenarios and practical applications. By means of electrospinning, 3D printing, hydrogel and nanotechnology, we can give full play to the pharmacological role of CBD to achieve oral and maxillofacial wound repair, tumor treatment, periodontal treatment, dental endodontic treatment and even the prevention and treatment of peri-implant inflammation, as shown in Fig. 4.
In the future, with the deepening of CBD research and the establishment of its clinical evidence-based medicine, many dental products and patents will be generated. The drug delivery route also requires more specificity and refinement to meet the treatment needs of patients with different oral diseases. As the proportion of older people in the global population increases, so does the need for age-related drug delivery systems for older people, it is particularly important to be able to self-administer drugs and provide simpler, more timely and targeted drug delivery systems [193], [197]. At the same time, in order to improve the administration efficiency and bioavailability of CBD, some physicochemical technologies to promote CBD penetration have also become an indispensable way. For example, in chemical methods, excipients are used to promote the distribution and diffusion of CBD drugs in the skin. Other physical methods include electroacoustic therapy, laser and magnetic energy, and can even be thermal, mechanical and pressure-based techniques [263]. In addition, in order to achieve more convenient and effective delivery and treatment of CBD, the future nanomedicine delivery platform is also the highlight of its research. These include liposomes [264], polymer nanoparticles [265], nanoemulsions [266], solid lipid nanoparticles [267], and nanostructured lipid carriers [268], among others [269]. To sum up, with the in-depth research on CBD and its receptors, the extensive pharmacological effects of CBD will provide a new idea and research value for the treatment of oral diseases, and more practical alternative products for CBD oral treatment may be found in the future. These alternative products will also provide accurate, safe, effective and convenient delivery routes for oral disease treatment.
6. Conclusions
In short, with the in-depth study of oral CBD receptors and the disclosure of pharmacological effects, it has a potential application prospect in the treatment of oral diseases. It is worth noting that CBD’s analgesic, antioxidant, anti-inflammatory, antibacterial, antipruritic and anticancer properties can be used for the treatment of dental pulp diseases, periodontal diseases, oral mucosal diseases, oral tumors, temporomandibular joint diseases and trauma infections. However, further studies are needed to verify the safety and efficacy of CBD in the clinic. In addition, CBD also needs in-depth research and excavation in the administration of oral diseases. It is believed that with the research and exploration of a large number of scholars, CBD can be truly applied to the dental field in the form of pharmaceutical or tissue engineering stent load. At the same time, it is hoped that more and more researchers will devote themselves to CBD research, paving the way for the implementation of CBD formulation patents and product development in dentistry.
Ethics approval
No ethical approval was required for this study.
Funding statement
Competitive Projects for Science and Technology Innovation and Development of Gansu Province (2018ZX-10); Gansu provincial key research and development project – International science and technology cooperation (22YF7WA013); Clinical research project of Hospital of Stomatology Lanzhou University (lzukqky-2022-t06); Lanzhou Talent Innovation and Venture Project (2017-RC-31); CSA West China Clinical Research Fund (CSA-W2022-11).
Author statement
All authors wrote the manuscript. All authors have read and approved the final manuscript.
CRediT authorship contribution statement
Zonghao Hu: Writing – original draft, Visualization, Validation. Zishun Qin: Writing – original draft, Visualization. Jinhong Xie: Writing – original draft, Visualization. Yue Qu: Writing – original draft. Lihua Yin: Review and editing, Project administration,Validation, Supervision.
Declaration of Competing Interest
All authors declare no conflict of interest regarding the present work and they have no involvements that might raise the question of bias in the work reported or in the conclusions, implications or opinions stated.
Data availability
No data was used for the research described in the article.
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