Canna~Fangled Abstracts

Tetrahydrocannabinol-Rich Extracts From Cannabis Sativa L. Improve Glucose Consumption and Modulate Metabolic Complications Linked to Neurodegenerative Diseases in Isolated Rat Brains

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Journal List > Front Pharmacol > v.11; 2020 > PMC7774498

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. 2020; 11: 592981.
Published online 2020 Nov 24. doi: 10.3389/fphar.2020.592981
PMCID: PMC7774498
PMID: 33390972
Ochuko L. Erukainure, 1 Motlalepula G. Matsabisa, 1 ,* Veronica F. Salau, 2 and Md. Shahidul Islam 2
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Abstract

Reduced brain glucose consumption arising from impaired glucose uptake and utilization has been linked to the pathogenesis and complications of neurodegenerative diseases. The ability of Cannabis sativa L. tetrahydrocannabinol (THC)-rich extracts to stimulate brain glucose uptake and utilization as well as its modulatory effect on gluconeogenesis, antioxidative, purinergic and cholinergic activities were investigated in isolated rats’ brains. C. sativa leaves were sequentially extracted to yield the hexane and dichloromethane extracts. The extracts were incubated at 37°C with freshly harvested brains in the presence of glucose for 2 h. The control consisted of incubation without the extracts, while brains without the extracts and glucose served as the normal control. Metformin was used as the standard drug. C. sativa extracts caused a significant (p < 0.05) increase in brain glucose uptake, with concomitant elevation of glutathione level, superoxide dismutase, catalase, and ecto-nucleoside triphosphate diphosphohydrolase activities compared to the controls. Incubation with C. sativa extracts also led to depletion in malondialdehyde and nitric oxide levels, acetylcholinesterase, butyrylcholinesterase, glucose 6-phosphatase and fructose-1,6-biphosphatase activities. GC-MS analysis of the extracts revealed the presence of THC. In silico analysis predicted THC to be permeable across the blood-brain-barrier. THC was also predicted to have an oral LD50 and toxicity class values of 482 mg/kg and 4 respectively. These results indicate that C. sativa improves glucose consumption with concomitant suppression of oxidative stress and cholinergic dysfunction, and modulation of purinergic and gluconeogenic activities in brain tissues

 

Keywords: brain glucose consumption, Cannabis sativa, neurodegenerative diseases, tetrahydrocannabinol 3, carbohydrate metabolism

Introduction

The brain’s dependence on glucose for energy generation is well documented. Brain glucose homeostasis has also been reported to be important for neuronal generation and maintenance, regulation of neurotransmitter, cognitive function and synaptic plasticity (). Glucose transporters aid in transporting glucose across the blood brain barrier (BBB) from the blood stream to the brain. Altered glucose homeostasis in the central nervous system (CNS) has been reported in most neurodegenerative diseases such as Alzheimer’s and Parkinson diseases (). This has been attributed to abnormalities in insulin signaling pathways in the brain as well as alteration of the glucose transporters at the BBB (; ). These abnormalities and alterations often cause deceased brain glucose consumption which can lead to a hypometabolic brain state characterized by glucose dysmetabolism (). Thus, making the brain susceptible to degenerative diseases. This is evident in studies which correlated the risk of Alzheimer’s disease with reduced brain glucose metabolism ().

Increased oxidative stress has been linked with decreased brain glucose uptake (). Increased glucose uptake has been shown to improve proteostasis which causes an upregulation of the unfolded protein response that protects against endoplasmic reticulum stress (; ). Oxidative stress has been implicated in the etiology and pathogenesis of neurodegenerative diseases (; ). This is evident in the use of antioxidants in treating and managing most neurodegenerative diseases such as Alzheimer’s and Parkinson’s diseases (; ). Antioxidants have been reported for their ability to scavenge free radicals as well as improve the activities of the endogenous antioxidant enzymes (). Oxidative stress has also been implicated in the disturbances of cholinergic and purinergic enzymes activities of the CNS (; ). These enzymes have been reported for their respective neurotransmission and bioenergetic roles which are critical for normal functioning of the brain (; ).

Cannabis sativa L. is among the medicinal plants used in the treatment and management of neurological diseases. It is an annual herbaceous plant that belongs to the Cannabis genus and Cannabaceae family. It is globally distributed, with Africa accounting for 25% of its global production (). Its common names include weed, Indian hemp and marijuana. C. sativa is utilized for food, therapeutic, recreational and religious purposes (). Phytocannabinoids make up the major phytochemical constituents of C. sativa, with tetrahydrocannabinol (THC), cannabinol, and cannabidiol among the most common (). The therapeutic role of C. sativa against neurodegenerative diseases and other psychopathic ailments have been reported (; ; ). The aqueous and ethanol extracts of the leaves have been reported to confer protective effects on α-motor neurons via antioxidative and anti-apoptotic activities (). Cannabidiol has been reported for its ability to activate metabotropic receptors for serotonin and/or adenosine as well as nuclear receptors of the PPAR family (). The leaves improved tremor, bradykinesia and rigidity in Parkinsonian patients (). The neuroprotective effects of C. sativa have been demonstrated on basal ganglia disorders (). Other reported medicinal properties of C. sativa include anti-diabetes (), anticancer (), pain suppression (), anti-epilepsy (), and sleep management ().

Despite the reported neuroprotective effect of C. sativa and its phytoconstituents, there are still dearth in its ability to promote brain glucose uptake and/or utilization. Thus, this present study was aimed at investigating the ability of the leaves to stimulate glucose uptake and utilization, as well as its modulatory effect on antioxidative, purinergic and cholinergic activities, and gluconeogenesis in isolated brains. The cytotoxic effect of the leaves was also investigated in glioblastoma multiforme (U87 MG) cells.

Materials and Methods

Plant Permit Approval

This research has been undertaken under the permit approval (Permit No. POS 248/2019/2020) from the South African Health Products Regulatory Authority to conduct, collect, posses, transport and store cannabis plant, plant parts and products for research purposes. The study was also conducted to collect cannabis plants in Lesotho under the permit (Permit #: 01/LS/2019/10/02-01).

Plant Material

Cannabis sativa leaves were obtained from Mohale’s Hoek District, Lesotho (GPS coordinates: −30.333776″S and 27.651201″E). They were authenticated by the Geo Potts Herbarium at the University of the Free State, Bloemfontein 9300, South Africa and assigned the voucher number, BLFU MGM 0018. The leaves were pulverized to dry powder, after air drying to a constant weight.

The powdered samples were thereafter sequentially extracted with solvents of increasing polarity vis-à-vis hexane and dichloromethane (DCM) for 48 h with mild agitation of 100 rpm at room temperature. The solvents were respectively decanted and concentrated in vacuo using an R–215 rotary evaporator (Buchi, Switzerland). The extracts were collected in glass vials and stored in the dark at ambient room temperature for further ex vivo studies.

Animals

A day to the experiment, sixteen male albino rats (Sprague Dawley strain) weighing 180 – 200 g were obtained from the Biomedical Research Unit, University of KwaZulu-Natal, Durban, South Africa and housed in plastic cages. They were fasted for 8 h before humanely sacrificed by euthanizing with Isofor. Their brains were harvested and rinsed in normal saline to remove blood stains. Each brain was divided into its hemispheres and used immediately for ex vivo study.

Glucose Uptake in Isolated Rat Brain

Each hemisphere of the freshly harvested rat brains was incubated in 8 ml of Krebs buffer containing 11.1 mM glucose and the different concentrations of C. sativa extracts (hexane and DCM) for 2 h under a 5% CO2, 95% oxygen and 37°C conditions as described in previously published methods (; ). The untreated control consisted of incubation without the extracts, while brains incubated without the extracts and glucose served as the normal control. Metformin was used as the standard drug. Each treatment group consisted of 3 brain hemispheres.

After incubation, the brain tissues were collected and homogenized in 50 mM phosphate buffer (pH 7.5) with 1% triton X-100, and thereafter centrifuged at 15,000 rpm at 4°C for 10 min (). The supernatants were collected and stored at −20°C until further analysis.

The study was carried out under the approved guidelines of the animal ethics committee of the University of KwaZulu-Natal, Durban, South Africa (protocol approval number: AREC/020/017D).

Determination of Glucose Utilization

Aliquots from the incubating buffer was collected prior and after the incubation for determination of glucose utilization. This was carried out by measuring the glucose concentrations using an automated chemistry analyzer (Labmax Plenno, Labtest Inc., Lagoa Santa, Brazil). Glucose utilization was thereafter calculated with the formula:

Glucose uptake=GC1−GC2 Weight of brain tissue (g)

Where GC1 and GC2 are glucose concentrations (mg/dL) before and after incubation, respectively.

Determination of Antioxidative Activity

Reduced glutathione level

The Ellman’s method () was used in determining the GSH level of the brain tissue. Briefly, the resulting supernatant was deproteinized with an equal volume of 10% Trichloroacetic acid (TCA) and centrifuged for 5 min at 3,500 rpm. 200 μl aliquot was collected from the deproteinized sample into a 96 well plate. 50 μl of Ellman reagent was thereafter added and the reaction mixture was allowed to stand for 5 min. Absorbance was read at 415 nm. The GSH concentration was extrapolated from a standard curve.

Superoxide dismutase Activity

The superoxide dismutase (SOD) activity of the brain tissues was determined using a method based on the principle that 6-hydroxydopamine (6-HD) is oxidized by H2O2 from SOD catalyzed dismutation of O2 −, which produces a colored product (). Briefly, 15 μl of the tissue supernatants were dissolved in 170 μl of 0.1 mM diethylenetriaminepentaacetic acid (DETAPAC) in a 96 well plate. Thereafter, 15 μl of 1.6 mM 6-HD was added. Absorbance was measured at 492 nm for 5 min at 1 min interval.

Catalase Activity

The catalase activity of the brain tissue was determined using a previously established protocol (). Briefly, 10 μL of the tissue supernatants was mixed with 340 μL of 50 mM sodium phosphate buffer (pH 7.0). Thereafter, 150 μL of 2 M H2O2 was added to the reaction mixture. Absorbance was read at 240 nm at 1 min interval for 3 mins.

Lipid Peroxidation Level

The lipid peroxidation level of the brain tissues was determined by measuring the thiobarbituric acid reactive substances (TBARS) in the tissues and expressed as malondialdehyde (MDA) equivalent (). Briefly, a reaction mixture consisting of 100 μl of the supernatants, 100 μl of 8.1% SDS solution, 375 μl of 20% acetic acid, 1 ml of 0.25% thiobarbituric acid (TBA), and 425 μL of distilled water was heated at 95°C for 1 h in a water bath. A 200 μl aliquot was thereafter collected from the reaction mixture into a 96 well plate, and absorbance read at 532 nm.

Nitric Oxide Level

The brain tissues were assayed for nitric oxide level using the Griess method as previously described (; ). Briefly, 100 μl of the tissue samples and/or distilled water (blank) were incubated with an equal volume of Griess reagent for 30 min at 25°C in the dark. Absorbance was read at 548 nm.

Cholinergic Enzymes Activities

The brain tissues were assayed for cholinergic activities by analyzing the activities of acetylcholinesterase () and butyrylcholinesterase () respectively in the tissue supernatants. Briefly, 20 μl of the tissue supernatants was incubated with 10 μl of 3.3 mM Ellman’s reagent (pH 7.0) and 50 μl of 0.1 M phosphate buffer (pH 8) for 20 min at 25°C. For acetylcholinesterase activity, the reaction was stopped by adding 10 μl of 0.05 M acetylcholine iodide to the reaction mixture. While 10 μl of 0.05 M butyrylcholine iodide was used to stop the reaction for butyrylcholinesterase activity. Absorbances were read at 412 nm at 3 min intervals.

Purinergic Enzymes Activities

Th brain tissues were assayed for purinergic activities by analyzing for the activity of ecto-nucleoside triphosphate diphosphohydrolase (E-NTPDase) () in the tissue supernatants. Briefly, 20 µl of the tissue supernatants was incubated with 200 µl of the reaction buffer (1.5 mM CaCl2, 5 mM KCl, 0.1 mM EDTA, 10 mM glucose, 225 mM sucrose and 45 mM Tris-HCl) at 37°C for 10 min 20 µl of 50 mM ATP was added to the reaction mixture and further incubated at 37°C for 20 min in a shaker. The reaction was stopped with 200 µl of 10% TCA and incubated on ice for 10 min. Absorbance was read 600 nm.

Determination of Gluconeogenic Enzymes Activities

The gluconeogenic enzymes activities of the brain tissues were determined by analyzing the supernatants for glucose 6 phosphatase (; ), and fructose-1,6-bisphosphatase (; ) activities with slight modifications.

To determine glucose 6 phosphatase activity, 200 µl of the tissue supernatants was incubated with 100 µl of 0.25 M glucose, 200 µl of 5 mM KCl, 1300 µl of 0.1 M Tris-HCl buffer, and 40 µl of 50 mM ATP at 37°C in a shaker for 30 min. The reaction was stopped with 1 ml of distilled water and 1.25% ammonium molybdate. 1 ml of freshly prepared 9% ascorbic acid was then added to the reaction mixture and allowed to stand for 30 min. Absorbance was read at 660 nm. ATPase activity was calculated as the amount of inorganic phosphate (Pi) released/min/mg protein.

For fructose-1,6-biphosphatase activity, 100 µl of the tissue supernatant was incubated with 1,200 μl of Tris–HCl buffer (0.1 M, pH 7.0), 100 μl of fructose (0.05 M), 250 μl 0.1 M MgCl2, 100 μl 0.1 M KCl, and 250 μl 1 mM EDTA at 37°C for 15 min. The reaction was stopped with 1 ml of 10% TCA and incubated on ice for 10 min. Absorbance was read at 680 nm and the activity calculated as the amount of inorganic phosphate (Pi) released/min/mg protein.

3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide Assay

Cell Lines and Cell Culturing

The human U87 MG glioblastoma cancer (ATCC® HTB-14™) cell line was obtained from the American Type Culture Collection (ATCC, Virginia, United States). Dulbecco’s Minimum Essential Media (DMEM), Eagle’s Minimum Essential Media (EMEM), Fetal bovine serum (FBS) and Phosphate Buffer Saline (PBS) were purchased from Life technologies (Pty) Ltd. (Fairlands, Johannesburg, RSA). The 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT), Dimethyl Sulfoxide (DMSO), Trypsin, and all other chemicals and reagents were of analytical grade and acquired from Merck (Pty) Ltd. (Modderfontein, Johannesburg, RSA). The U87 cell line was maintained in DMEM:EMEM (1:1), supplemented with 10% heat-inactivated FBS and grown at 37°C in a humidified incubator set at 5% CO2. Cells were sub-cultured with 0.25% (w/v) trypsin 0.53 mM ethylenediaminetetraacetic acid (EDTA) for a maximum of 15 min every 2 and 3 days after they had formed an 80% confluent monolayer.

Cell Proliferation Assay

To analyze the effect of the samples on the cell viability, the MTT method was utilized. Cells were seeded in 100 µl medium in 96-well microtiter plates at a concentration of 1 × 105. Stock solutions of 4 mg/ml of the samples were prepared in 20% ethanol. The positive control, doxorubicin was dissolved in 50% DMSO to obtain a stock concentration of 10 mg/mL. Serial dilutions were made to achieve target concentrations of the samples and doxorubicin in a of range 30, 60, 120, 240 μg/ml and 12.5–100 μg/ml, respectively. Subsequently, cells were exposed to the samples, doxorubicin and the controls, which included vehicle-treated cells exposed to 1.2% ethanol or 0.5% DMSO and cells propagated in growth medium. After the 48 h treatment period, the cells were subjected to the МТТ reagent (0.5 mg/mL). The colorimetric reaction was measured by means of a plate reader (Multiskan Go, Thermofischer Scientific) at 570 nm wavelength. Color control blanks were included and utilized to normalize the results and the vehicle control treated cells were regarded as 100% cell viability. The samples were evaluated in atleast three independent experimental repeats and each sample was evaluated in triplicate for each experimental repeat. The results given are representative of the average percentage inhibition of all the experimental repeats.

GC-MS analysis of Cannabis sativa Extracts

Apparatus

An Agilent technologies 6890N GC-MS machine coupled with a 5973-network mass selective detector was used for the analysis. An Agilent technologies 7683 Series injector and screw neck glass vials (separations) were used for sample injection.

GC-MS Conditions

The extracts were analyzed using a HP-5ms capillary column phase. The injection volume was set to 2 µl at 80°C. the flow rate of the helium gas was 1 ml/min at a constant flow. The oven program was set at 80°C for 2 min and increased to 300°C at 20°C/min for 3 min. A mass selective detector was used for the detection of the volatile compounds present in the standards and tests samples. The NIST mass spectral library database software was used to analyze the data. The mass spectrometer data system has a reporting software module that combines the data results with the NIST library and ADMIS software search for target compounds into a single report.

In Silico Prediction of Blood Brain Barrier Permeability and Oral Lethal Dose Toxicity

The ability of the GC-MS identified compound to cross the BBB was predicted in silico using the SwissADME online server (http://www.swissadme.ch/index.php) (). Its oral lethal dose toxicity (LD50) and toxicity class were predicted using the PROTOX II online server (http://tox.charite.de/protox_II/) (). These were done by obtaining the Canonical SMILES of the GC-MS identified compound from PubChem (https://pubchem.ncbi.nlm.nih.gov/), and computed into the respective servers for the predictions.

Statistical Analysis

Data were subjected to one-way ANOVA and presented as mean ± SD. Significant differences between means at p < 0.05 were obtained using the Tukey’s HSD-multiple range post-hoc test. Statistical analyses were done using IBM Statistical Package for the Social Sciences (SPSS) for Windows, version 23.0 (IBM Corp., Armonk, NY, United States).

Results

Incubation of brain tissues with glucose in the presence of hexane and DCM extracts of C. sativa leaves led to significant (p < 0.05) increase in glucose utilization, with the DCM extract having a higher activity as depicted in Figure 1. The activity was dose-dependent, with the highest concentration having the highest activity. Incubation with metformin had no significant effect on brain glucose utilization.

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Effect of Cannabis sativa on glucose uptake in brain tissues. *abValues with different letter above the bars for a given extract are significantly (p < 0.05) different from each other.

Incubation of brain tissues with glucose led to significant (p < 0.05) depletion in the levels of GSH, SOD and catalase activities, while significantly elevating MDA level as shown in Figures 2A–D. Incubation with the extracts significantly (p < 0.05) reversed these levels and activities dose-dependently to near normal.

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Effect of Cannabis sativa on (A) glutathione (GSH) level, (B) superoxide dismutase (SOD) activity, (C) catalase activity, and (D) malondialdehyde (MDA) level in brain glucose uptake. Value = mean ± SD; n = 3. *Statistically significant (p < 0.05) compared to glucose-treated tissue; #statistically significant (p < 0.05) compared to normal tissue. Normal, No glucose/C. sativa.

As shown in Figure 3, incubation with glucose led to significant (p < 0.05) elevation of NO level in brain tissues. This level was significantly (p < 0.05) depleted on incubation with C. sativa extracts.

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Effect of Cannabis sativa on NO level in brain glucose uptake. Values = mean ± SD; n = 3. *Statistically significant (p < 0.05) compared to glucose-treated tissue; #statistically significant (p < 0.05) compared to normal tissue. Normal, No glucose/C. sativa.

There was a significant (p < 0.05) elevation in acetylcholinesterase and butyrylcholinesterase activities in brain tissues incubated with glucose as depicted in Figures. 4A,B. The acetylcholinesterase activity was significantly (p < 0.05) reversed dose-dependently on incubation with DCM extract (Figure 4A). However, the hexane extract significantly (p < 0.05) elevated acetylcholinesterase activity dose-dependently (Figure 4A). Both extracts significantly (p < 0.05) depleted butyrylcholinesterase activity in a dose-dependent manner (Figure 4B).

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Effect of Cannabis sativa on (A) acetylcholinesterase and (B) butyrylcholinesterase activities in brain glucose uptake. Values = mean ± SD; n = 3. *Statistically significant (p < 0.05) compared to glucose-treated tissue; #statistically significant (p < 0.05) compared to normal tissue. Normal, No glucose/C. sativa.

As shown in Figure 5, there was a significant (p < 0.05) depletion in E-NTPDase activity in brain tissues incubation with glucose only. Incubation with C. sativa extracts led to significant (p < 0.05) reversion of the activity to levels indistinguishable from the normal tissues.

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Effect of Cannabis sativa on ecto-nucleoside triphosphate diphosphohydrolase activity in brain glucose uptake. Values = mean ± SD; n = 3. *Statistically significant (p < 0.05) compared to glucose-treated tissue; #statistically significant (p < 0.05) compared to normal tissue. Normal, No glucose/C. sativa.

As depicted in Figures. 6A,B, there was a significant (p < 0.05) elevation in the activities of glucose 6-phosphatase and fructose-1,6-biphostase in brain tissues incubated with glucose only. These activities were significantly (p < 0.05) reversed in tissues incubated with C. sativa extracts to levels indistinguishable from the normal tissues.

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Effect of Cannabis sativa on (A) glucose 6-phosphatase and (B) fructose-1,6-biphosphatase activities in brain glucose uptake. Values = mean ± SD; n = 3. *Statistically significant (p < 0.05) compared to glucose-treated tissue; #statistically significant (p < 0.05) compared to normal tissue. Normal, No glucose/C. sativa.

MTT assay revealed C. sativa extracts had little or no cytotoxic effect on U87 MG cells, while doxorubicin significantly (p < 0.05) inhibited the proliferation of the cells as depicted in Figure 7.

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Cytotoxic effect of (A) Cannabis sativa and (B) doxorubicin on glioblastoma multiforme (U87 MG) cells. Values = mean ± SD; n = 3.

GC-MS analysis of the extracts revealed the presence of THC in both extracts as shown in Figure 8; Supplementary Figure S1.

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Tetrahydrocannabinol identified from the hexane and DCM extracts of C. sativa.

In silico BBB permeability prediction revealed THC to be permeable across the BBB as shown in Table 1. THC was further predicted in silico to be in the toxic class of 4, with a LD50 value of 482 mg/kg.

TABLE 1

In silico prediction of BBB permeability and toxicity of tetrahydrocannabinol.

In Silico activity Predictions
LD50 482 mg/kg
Toxicity class 4
BBB permeability Yes

BBB, blood brain barrier; LD50, ethal dose.

Discussion

Impaired brain glucose uptake leading to diminished neuronal glucose consumption has been linked to the pathogenesis and progression of neurodegenerative diseases such as Alzheimer’s and Parkinson’s diseases (; ). In the present study, the increased glucose uptake in brain tissues incubated with C. sativa extracts (Figure 1) indicates an increased glucose utilization which insinuates an increased neuronal glucose consumption. This activity portrays a facilitative uptake potential of C. sativa leaves which corresponds with previous studies on the use of medicinal plant leaves in facilitating brain glucose uptake (). This activity can be attributed to the GC-MS identified compound in the extracts, THC (Figs. 8 and S1) which can bind and activate the cannabinoid receptors of the endocannabinoid anandamide transporters at the BBB (). Thus, facilitating transportation across the BBB.

Oxidative stress and proinflammation have been implicated in the pathogenesis of neurological diseases, and have been reported among the major mechanisms in the etiology of the diseases (; ). The depleted GSH level, SOD and catalase activities on incubation of brain tissues with glucose (Figures. 2A–C) insinuates an oxidative state. This is further revealed by the exacerbated MDA level (Figure 2D) which indicates an occurrence of lipid peroxidation. This is in agreement with previous studies on exacerbated oxidative activities in brain tissues incubated with glucose (). The brain has been reported for its high susceptibility to oxidative stress owing to its polyunsaturated fatty acids contents, redox-active metal load, low endogenous antioxidant system, and auto-oxidizable neurotransmitters dependence (; ; ; ). The increased brain NO level (Figure 3) with concomitant low SOD activity on incubation with glucose may insinuate a proinflammatory effect. In the presence of depleted SOD activity, peroxynitrite (ONOO−) is generated from the reaction of NO and superoxide (O2−) (; ). Peroxynitrite has been reported for its potent proinflammatory roles in several diseases including neuropathy as it has been implicated in the pathogenesis of Alzheimer’s and Parkinson’s diseases, and multiple sclerosis (; ). Antioxidants have been reported for their therapeutic roles in the treatment and management of neurodegenerative diseases (; ). The elevated GSH level, SOD and catalase activities, with concomitant depleted levels of MDA and NO on incubation with C. sativa extracts indicate an antioxidative and anti-proinflammatory effect. THC has been reported for its potent antioxidant and anti-proinflammatory activities in the treatment and management of neurological diseases (; ; ). Thus, may be responsible for the antioxidative effect of the extracts.

Cholinergic dysfunction has been recognized as one of the major defects of neurodegenerative diseases such as Alzheimer’s, Parkinson’s diseases and multiple sclerosis (). It is characterized by increased activities of acetylcholinesterase and butyrylcholinesterase which catalyze the hydrolysis of the neurotransmitter acetylcholine (). Thus, implying that the elevated activities of these enzymes on incubation of brain tissues with glucose (Figures 4A,B) indicates a cholinergic dysfunction and may insinuate a neurodegenerative symptom. Several therapies have targeted the inhibition of these enzymes in the treatment and management of neurodegenerative diseases (; ). Thus, the inhibitory effect of the extracts on these enzymes portrays a neuroprotective activity of C. sativa. This corroborates previous reports on the inhibitory effect of C. sativa and its major phytochemical constituents on acetylcholinesterase and butyrylcholinesterase activities (; ). However, the increasing acetylcholinesterase activity with increasing concentration of the hexane extract (Figure 4A) may insinuate the inhibitory effect of the extract on the enzyme diminishes with increasing concentrations.

The depleted E-NTPDase activity in brain tissues incubated with glucose (Figure 5) indicates a depleted adenosine level which portrays a decreased purinergic activity. Impaired purinergic activity has been implicated in the pathogenesis of neurodegenerative diseases (; ). It is characterized by decreased production of adenosines which are involved in energy transfer reactions and facilitative transportation (). The increased E-NTPDase activity in brain tissues incubated with C. sativa extracts insinuates the ability of C. sativa to improve neuronal purinergic activity.

Diminished brain glucose consumption is often characterized by increased glycogenolysis and impaired glycolytic flux to compensate for the low glucose level (; ). This has been implicated in the pathogenesis of Alzheimer and other neurodegenerative diseases (). In the present study, the depleted brain glucose consumption (Figure 1) corroborates with the exacerbated glucose 6-phosphatase and fructose-1,6-biphosphatase activities in brain tissues incubated in glucose (Figures. 6A,B). Both enzymes are involved in gluconeogenesis, with glucose 6-phosphatase and fructose-1,6-biphosphatase catalyzing the hydrolysis of glucose 6-phosphate to glucose in the glycogenolytic pathway and fructose-1,6-biphosphate to fructose 6-phosphate in the gluconeogenic pathway respectively. The continuous activation of these enzymes will lead to glucose accumulation which can serve as metabolite precursors for the hexosamine, polyol, protein kinase C, and AGE pathways which have been linked to the pathogenesis of neurodegenerative diseases (; ). Glucose has also been reported as an intermediate for the generation of free radicals, as it is oxidized in its enediol form into reactive ketoaldehydes and superoxide anion radicals (). Thus, the dose-dependent inhibited activity of these enzymes in brain tissues incubated with C. sativa extracts further indicates the neuroprotective effect of C. sativa.

Glioblastoma multiforme (GBM) is a malignant primary brain tumor common in young kids (). Studies have reported therapeutic failures in patients owing to difficulty in treatment (). Although medicinal plants have reported to arrest the proliferation of GBM (), C. sativa extracts showed no cytotoxic effect on the cells (Figure 7). Thus, insinuating that the plant may not be beneficial in the treatment of GBM.

The predicted ability of THC to permeate the BBB (Table 1) further connotes the neuroprotective effect of C. sativa and corroborates previous reports on the ability of cannabinoids to modulate the cannabinoid receptors of anandamide transport across the BBB (). The predicted oral LD50 and toxicity class values of THC (Table 1) indicates that the compound is relatively safe when orally consumed.

Conclusion

As portrayed by these results, C. sativa improves glucose consumption with concomitant suppression of oxidative stress and cholinergic dysfunction, and modulation of purinergic and gluconeogenic activities in brain tissues. Further studies are recommended to decipher the molecular mechanisms that may be involved in these neuroprotective activities in in vivo studies.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Ethics Statement

The animal study was reviewed and approved by The animal ethics committee of the University of KwaZulu-Natal, Durban, South Africa (protocol approval number: AREC/020/017D).

Author Contributions

MM and OE conceptualized and designed the research project; OE, VS and MI carried out the experiments; MM and OE wrote the original manuscript; all authors revised and approved the final manuscript draft; MM supervised the project.

Funding

Authors are thankful to IKS Based Technology Innovation Unit of DSI South Africa, for financial support (Grant contracts: DST/CON 0162/201 and DST/CON 0206/2019/2020) and University of the Free State for technical support and postdoctoral support for OE.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors are also thankful for the assistance and support from the Free State Provincial Police and the Police at Port St Johns and Lusikisiki in the Eastern Cape. The authors are further thankful to Mirranda Javu, senior community liaison officer, Department of Pharmacology UFS for community engagement and negotiations on the cannabis collections. Similar appreciation goes to LR Mafura and SE Molomo both from the Ministry of Forestry, Range, Soil & Water Conservation, Mafeteng, Lesotho for the assistance with the cannabis project and cannabis plants wild collections.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2020.592981/full#supplementary-material

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