Journal List > Acta Endocrinol (Buchar) > v.18(2); Apr-Jun 2022 > PMC9512370
Abstract
The discovery of the cannabinoid receptors CB1 and CB2 in 1990 and 1993, respectively, as well as of the two main endocannabinoids, anandamide in 1992 and 2-arachidonylglycerol in 1995, was an important step in identifying the strongest homeostatic system in the human body, namely the endocannabinoid system. Ever since, research has highlighted the crucial part played by this system in all the reproduction stages: folliculogenesis, spermatogenesis, oogenesis, fecundation, transport of the egg through the fallopian tubes, blastocyte implantation and pregnancy progression, as well as its implications in the physiopathology of the reproductive system: in endometriosis, ectopic pregnancy, miscarriage, preeclampsia, endometrial cancer, polycystic ovary syndrome, ovarian cancer. A special attention must be paid to the phytocannabinoids, natural components originating especially from the Cannabis plant inflorescences, whose medical effects are well-established nowadays with also acting on the receptors of the endocannabinoid system. The most recent research mainly focuses on the reproductive dysfunctions and disorders of the reproductive tissues, respectively, through its action upon the endocannabinoid system. Medical cannabis is nowadays legalized in more and more countries all over the world. At the same time, recreational cannabis remains one of the most consumed drugs (in Romania the most consumed one by young adults). Therefore, it is mandatory for specialists in obstetrics and gynecology, endocrinology, public health, hygiene or for general practitioners, to permanently update their information on this subject.
Introduction
In the last 2-3 decades, 50 countries world widely have legalized or decriminalized the medical use of cannabis. In Europe, 23 countries finalized the process of legalizing the use of medical cannabis, while other countries, among which Romania as well, have this problem on their agenda. At the same time, recreational cannabis remains one of the most used drugs. According to the National Report on Drug Situation in 2020 – New evolution and trends (1) the recreational cannabis consumption, although having the lowest rates in Europe, preserves its ever-growing trend, thus continuing to be the most consumed drug in Romania. The most frequent consumption rate is observed in the young population, of fertile age (15-34 years old), with the same sex ratio male/female 2/1, like in any other age groups. In Romania, one in 10 young adults (18-34 years old) has tried to smoke cannabis (10%), one in 20 smoked in the last year (5.8%) and 1 in 40 declared cannabis consumption when questioned (2.5%) (2).
Consequently, it is mandatory for the medical staff to be updated with as much information as possible regarding the endocannabinoid system, as well as with its impact on the reproductive system.
Therefore, the aim of the present editorial was to bring new insights on the endocannabinoid system, its main receptors, the metabolization pathways as well as its impact in women reproduction.
Short description of the endocannabinoid system in relation with the reproduction
Ever since the 15th Century there has been proof of the medical use of cannabis, during birth (3). Still, for many years, the most known side effects of recreational cannabis use on fertility are: it decreases the LH serum levels (4,5), inhibits prolactin secretion (6) increases testosterone serum level, disturbs menstrual cycle (7), causes a low rate of oocyte collection during the in vitro fertilization (IVF) treatment (8,9), negatively influences intrauterine fetal growth (10,11), increases premature birth incidence (12,13), low birth weight and prematurity (VLBW) (7), as well as difficult child delivery (14,15). Nevertheless, the mechanisms through which these produce their effect have not been clearly understood. The discovery of the cannabinoid receptors CB1 and CB2 in 1990 and 1993, respectively, as well as of the two main endocannabinoids, anandamide in 1992 and 2-arachidonylglycerol in 1995, were also the initial steps in identifying the strongest homeostatic system in the human body, namely the endocannabinoid system (ECS). The decades following the discovery clarified the role played by the ECS in all stages of reproduction: spermatogenesis, oogenesis, fecundation, transport of the egg through the fallopian tubes, blastocyte implantation and pregnancy progression. Also, the role of the ECS in the pathologies of the reproductive system was clarified: endometriosis, ectopic pregnancy, miscarriage, preeclampsia, endometrial cancer, polycystic ovary syndrome, ovarian cancer (16).
The endocannabinoid system (ECS) is defined as a group of receptors, ligands (endocannabinoids), enzymes of their synthesis and degradation and also their transmembrane transporters. Endocannabinoids (eCBs) are fatty acid derived lipids (most often arachidonic acid derivates) synthesized by the human body under the action of some specific enzymes, under a nervous or hormonal impulse, or of the cytokines signaling the cells. The best studied endocannabinoids are, anandamide (AEA) or N- arachidonoylethanolamide and 2-arachidonoylglyerol (2-AG).
The main receptors in the endocannabinoid system are:
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– CB1 receptors identified in the brain in 1990 (17); they are mainly found in the central nervous system and the spine, being the main psychoactive receptors, and also in the fatty tissue, liver, pancreas, skeletal muscles and immune cells, including most endocrine organs. They are also found in the ovaries, endometrium and testicles (18,19). Intracellularly, CB1 receptors are found on the external membrane of mitochondria (20). Mitochondria play an important role in the control of cellular apoptosis, their dysfunction affecting gametogenesis, embryogenesis and embryonic stem cell production (21). Mitochondrial dysfunction is also associated with oxidative stress in the placenta, thus leading to a vascular remodeling with an impact on the oxygenation and functioning of fetal organs (22,23).
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– CB2 receptors, identified in 1993, are mainly found in the peripheral nervous system and in the immune cells, in the cortex and ovarian medulla area, as well as in the ovarian follicles. CB2 are mainly immunomodulatory and anti-inflammatory receptors (24).
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– other identified receptors of ECS are transient receptor potential vanilloid-1 (TRPV1), peroxisome proliferator-activated receptors y (PPARy) and G protein-coupled receptor 18, 55 or 119 (GPR18, GPR55, GPR119) (25).
ECS is involved in multiple physiological processes, like nociception, cognitive function, mood regulation, appetite regulation, lipid metabolism, neurogenesis, neuroprotection, cell growth and proliferation etc. The receptor localization and the ligand type explain the effects of cannabinoids (26). For example, the CB1 receptors in the hypothalamus are involved in appetite regulation, those in the amygdale cause memory effects and emotional reactions, those in the peripheral nerves act upon pain sensation. Anandamide (AEA) has a partially agonist action on CB1 receptor. Endocannabinoid 2-arachidonoylglyerol (2-AG) acts like an agonist for both types of receptors. It should be specified that endocannabinoids act more as neuromodulators in the brain, with highly regulated, spatiotemporal specific patterns, than as neurotransmitters, due to their rapid synthesis, as well as fast degradation (27).
Ligands of the cannabinoid receptors may also be the phytocannabinoids present especially in the cannabis plant, as well as synthetic cannabinoids. The phytocannabinoids found in the cannabis plant are lipophilic terpeno-phenolic compounds, with a pharmacological action similar to that of endocannabinoids, still with a different structure (28).
More enzymes are responsible for the synthesis or catabolism of endocannabinoids, as shown in Figure 1. Endocannabinoids are neurotransmitters produced “on request” by a cell in membrane phospholipids (29).
Fatty acid amide hydrolase (FAAH) is the main enzyme responsible for the anandamide hydrolase into arachidonic acid (AA) and ethanolamine (EA). Anandamide (AEA) is synthesized from N-arachidonoyl-phosphati-dyetanolamine (NAPE) by phospholipase D (PLD) and it is decomposed by fatty acid amide hydrolase (FAAH) and cyclooxygenase 2 (COX-2), and 12-LOX into arachidonic acid, prostaglandin-ethanolamides or prostamides (PM) and 12-hydroxi-AEA (12-HAEA), respectively. NAPE, in its turn, comes from phosphatidylethanolamine under the action of N-acyltransferase (NAT). 2-arachidonoylglycerol (2-AG) is synthesized under the action of diacylglycerol lipase (DAGL) from diacylglycerol, being hydrolase by monoacylglycerol lipase (MAGL), COX-2, 12-LOX into arachidonic acid, prostaglandin glycerol ester (PG) and 12-HETE (12-hydroxyeicosatetraenoic acid) (31). Arachidonic acid is metabolized by COX-2, PGHS-1, PGHS-2 into prostanoids: prostaglandines (PGD2, PGE2, PGF2α), prostacyclin (PGI2) and thromboxane A2 (TxA2). Recently, there were also identified enzymes of the serine hydrolase family as regulators of the intracellular pool of 2-AG (30,32).
ECS involvement in women reproduction
Endocannabinoids, phytocannabinoids and synthetic cannabinoids have an impact during all the reproductive stages in women, from oocyte development to parturition, the cells and tissues of the reproductive organs being equipped with a completely functional ECS (8,32,33). Numerous studies showed the presence of ECS components in the serum, follicular fluid, ovary, uterus, placenta, endometrium, immune cells, as well as in the hypothalamus, having an important impact on fertility, reproduction and endocrine function (34). Apparently, most of them are present in the ovary, oviduct (35) and uterus (36).
ECS is engaged in the central control of the processes involved in reproduction: Gamete’s maturation takes place under the action of hypothalamic-pituitary-ovarian axis (HPO axis). ECS was identified in hypothalamic areas involved in the production of some hormones like gonadotropin releasing hormone (GnRH), acting through the HPO axis for the regulation of various reproductive processes (37). Endocannabinoids, their metabolic enzymes, and target receptors have been shown to respond to endocrine signals (38). The estrogen produced by the ovarian follicles inhibits FAAH, thus resulting high levels of AEA, with a role in follicle development and ovulation, followed by a decrease of FAAH inhibiting after ovulation, due to estrogen level decrease, and AEA degradation (39). The same AEA increases under the influence of estrogens and stimulates CB1 in the hypothalamus, thus leading to the reduction of GnRH release and inhibiting FSH and LH release in the pituitary, gonadal suppression and reduction of estrogen and progesterone levels (40). The levels of endocannabinoids are mildly regulated by the enzymes involved in their synthesis and degradation. High doses of exogenous cannabinoids (phytocannabinoids and synthetic cannabinoids) exert an inhibiting effect on the GnRH release (39).
The presence of CB1 receptors on the mitochondrial membrane allows endo and phytocannabinoids to influence the ovarian function and oogenesis, respectively. Still, it is interesting to observe that, in the ovarian follicles, CB2 receptors prevail comparing to CB1 ones, thus leading to the idea of an immunological part played primarily by the ECS in the ovarian function (19). AEA is produced by the follicular cells so that the concentration correlates with the follicular growth (41). In early stages of folliculogenesis, sustaining a low level of AEA allows the maturation of the oocyte, a maximum level of AEA being reached in the periovulatory phase (32). The AEA action on TRPV1 receptors in the spermatozoon facilitates the fusion with the oocyte (42,43). Multiple studies showed the presence of ECS components in the oviduct, more precisely AEA, NAPE-PLD, CB1, CB2, and FAAH (35,44). The transport through the oviduct of the fertilized egg and its growth into a morula are controlled by an AEA concentration gradient in the oviduct. This increase of the AEA level from the ampulla to the isthmus is maintained high by NAPE-PLD (the enzyme responsible for the synthesis) in the isthmus and low in the ampullar region, where FAAH (the enzyme responsible for degradation) is also high. Simultaneously, the FAAH expression increases in the embryonic cells that need to be protected from the AEA cytotoxicity (18). In the preimplantation embryos, CB1 and CB2 receptors are expressed, thus allowing AEA to influence the embryo growth through their activation (39). The low expression of CB1 receptors in the oviduct and decidua vera is apparently correlated with the ectopic pregnancy (45).
ECS modulates the endometrium plasticity and the uterus receptivity. AEA is considered to be the main factor enabling the synchronization between the embryo development and the endometrium, thus allowing its implantation during the so-called “implantation window” (Fig. 2) (46–51). AEA levels are high in non-receptive uteri and in the interimplantary areas in the receptive uterus, and low in receptive uteri and in implantary areas (low levels of NAPE-PLD and high FAAH activity and expression), thus leading to the idea that a balanced endocannabinoid system is essential for the synchronization between embryo implantation and endometrium preparation for it (37). The trophoblast differentiation is mildly controlled by AEA.
Its survival is favored by the FAAH increase, while this enzyme expression is stimulated by the pro-fertility signaling of leptin, progesterone and cytokines T Helper 2 (Th2) and inhibited by the anti-fertility signaling of cytokines T Helper 1 (Th1) (52). There are studies showing that the plasma and ovary AEA levels have a positive correlation (46). Low FAAH levels and high AEA levels in peripheral blood are associated with a hight risk of miscarriage, or with the failure of in vitro fertilization (53). Placenta formation is accompanied by decrease of CB1 receptors and increase of FAAH, while delivery is accompanied only by CB1 increasing. The AEA plasma level decreases from the first to the second trimester of pregnancy, without any other differences between the AEA plasma levels during the second and third trimesters up to a sudden increase during delivery. Most probably, this increase leads to the prostaglandin level increase through an AEA degradation and arachidonic acid release (54) (Fig. 3).
There is enough evidence regarding the effect of progesterone and estrogen on the ECS involvement in women fertility. During the menstrual cycle, the progesterone level is well-correlated with FAAH, and also with a the AEA plasma level, with which it has no correlation in early pregnancy (54). Progesterone has the following effects: during the implantation, FAAH decreases and reduces AEA; it plays a part in sustaining pregnancy through the stimulation of the synthesis of pro-fertility cytokines produced by type 2 helper (Th2), inhibiting the anti-fertility ones produced by type 1 helper (Th1) (55); it stimulates the production of leukemia inhibitor factor (LIF) mediated by IL-4, which sustains nidation and pregnancy (56). The estrogen level is positively correlated with the plasmatic AEA level during the menstrual cycle and in non-gestational women after in vitro fertilization and embryo transfer (57). A better predictability of AEA levels is difficult to attain due to the opposite effects of estrogen on NAPE-PLD in various tissues. 17β-Estradiol has the following effects: during folliculogenesis, it stimulates the NAPE-PLD activity and increases the AEA level in the endothelial cells, while, during implantation, it inhibits the FAAH activity and increases the AEA level in the endothelial cells and also down-regulates NAPE-PLD activity and inhibits the FAAH activity in the uterus epithelium (58).
For sustaining pregnancy, AEA low levels and consecutively high levels of leukemia inhibitor factor (LIF) via CB1 receptors are essential (59). LIF is an IL-6 with a role in the proliferation, differentiation and survival of cells, being important in the immune, hematopoiesis and reproduction processes. In humans, the LIF production was detected in the endometrium, reaching a peak during nidation, followed by a decrease towards the end of the luteal phase. The LIF production also exists in the fallopian tubes, being involved in the development and differentiation of the blastocyte. In women with idiopathic infertility or recurrent abortions there was observed a low production of LIF (60).
Also, the immunity adaptation through peripheral T lymphocytes represents a sine-qua-non production for a normal pregnancy. Progesterone induces the pro-fertility cytokines produced by type 2 helper (Th2), involving the CB2 receptor as well. The response of Th1 anti-fertility cytokines is inhibited by Th2 cytokines. AEA acts upon T cells through the CB1 receptor, thus reducing the LIF release in these cells (61).
Another cytokine, leptin, produced by the obese gene (ob) expression in the fatty tissue, ovary and placenta, has an effect on the ECS involvement in pregnancy by stimulating the FAAH activity and consecutive decrease of AEA level (62). Leptin level varies during the menstrual cycle, being lower during the follicular phase than in the secretory one (63). Pregnant women have higher concentrations of serum leptin than non-pregnant. Leptin was identified in the placental syncytiotrophoblast and the endometrium, as well. It plays an important part in reproduction, modulating the growth and development of conception product, with a possible involvement in the angiogenetic processes during early pregnancy (64). Also, it plays a role in the nidation process, the blastocyte presence stimulating its endometrial secretion, and in sustaining pregnancy, with serum levels higher in pregnant women and lower in women undergoing miscarriage during the first trimester (65,66).
Phytocannabinoids mimic the endocannabinoid action, the former being natural components from the inflorescence of Cannabis plant. At present, phytocannabinoids are also attributed medical effects, explained by their action on the human cannabinoid receptors, the medical use of cannabis being completely different from its recreational use. These facts bring back to our attention the Cannabis plant, also explaining the continuous global actions for legalizing medical Cannabis products.
In conclusion, up to the present time, the involvement of endocannabinoids in the regulation of food intake and energy homeostasis of the body, as well as their impact on the endocrine system, including the activity of the pituitary, adrenal cortex, thyroid, pancreas, and gonads (67) were highlighted.
Research performed in the last 20 years showed a major involvement of the ECS in the central and local control of processes related to reproduction. It is well-known the fact that disbalances of the ECS may lead to disorders related to the reproductive system, such as ectopic pregnancy, miscarriage, preeclampsia or conditions caused by the alteration of hormonal homeostasis, like endometriosis or gynecological cancers (45,47,61,68–72).
In the literature, AEA is already proposed as a potential biomarker for pregnancy progression, while the FAAH concentration in peripheral blood is considered a biomarker for infertility (69). Most recent studies focus on the treatment of reproductive dysfunctions, through the manipulation of the endocannabinoid system; nevertheless, there are numerous challenges to overcome in this direction (26), just like it is still difficult to talk about elements of the ECS as biomarkers for various physiological and pathological processes, due to their lack of specificity, with small exceptions, like the heterogeneity and complexity of the ECS.
The connection between the endocannabinoid system and the reproductive system represents an area of great interest that should definitely be known, in the context of legalizing medical use of cannabis in more and more countries all over the world, and whose thorough research may lead to new solutions for women with problems of the reproductive system.