Abstract
An emerging body of evidence implicates peripheral and central endocannabinoid pathways in the regulation of feeding behavior and body weight. A report in this issue of the JCI demonstrates the presence of a common endocannabinoid-regulated molecular pathway for peripheral lipogenic and central appetitive regulation. This pathway involves the activation of the transcription factor SREBP-1c and its associated enzymes, acetyl-CoA carboxylase-1 and fatty acid synthase, in the liver and hypothalamus. Activation of cannabinoid receptor 1 (CB1) in liver plays a key role in increased serum lipid production, fatty liver, and possibly diet-induced obesity. Conversely, stimulation of these receptors in the hypothalamus may lead to an increase in food consumption. Thus, targeting both of these pathways with CB1 antagonists could promote sustained weight loss and favorable serum lipid profiles in obese patients.
Cannabis has been used since antiquity for the treatment of many ailments, including pain, rheumatoid arthritis, epilepsy, and eating disorders. William O’Shaughnessy played a leading role in introducing this substance to Western medicine in the middle of the eighteenth century. One of the many pharmacological properties of cannabis he described was the induction of a “remarkable increase of appetite” (1). Over 120 years later, Gaoni and Mechoulam identified the structure Δ9-tetrahydrocannabinol (Δ9-THC) as the primary psychoactive constituent of cannabis (2). A considerable amount of preclinical research validated these early reports of the effects of cannabis on feeding by demonstrating that low-to-moderate doses of Δ9-THC and other cannabinoid receptor agonists increase feeding or food-motivated behavior (3). Importantly, administration of oral Δ9-THC (Marinol) was found to have some efficacy in treating the AIDS wasting syndrome by enhancing appetite and preventing weight loss (4).
Δ9-THC, along with other naturally occurring and synthetic cannabinoids, binds to 2 separate G protein–coupled receptors: cannabinoid receptor 1 (CB1), which is located in both the CNS and periphery (5), and CB2, which is found primarily on cells of the immune system (6). These receptors and their endogenous ligands, which include the fatty acid amide N-arachidonoyl ethanolamine (anandamide) and the monoacyl-glycerol 2-arachidonoylglycerol (2-AG) (7, 8), together constitute an endogenous cannabinoid (endocannabinoid) system. This system has been proposed to modulate several physiological functions, including pain (9, 10), cognition (11, 12), drug dependence (13), excitotoxicity (14), and feeding (15).
Endocannabinoid regulation of feeding and lipogenesis
A common experimental strategy to investigate whether the endocannabinoid system tonically modulates a physiological system is to disrupt CB1 signaling using either the CB1 antagonist SR141716 (Rimonabant) (16) or CB1–/– mice (13, 17). SR141716 administration has been shown to have an anorexic action in a variety of rodent models of feeding (3). In rats, it caused a dose-dependent decrease in consumption of either sucrose pellets or sucrose solution, but had limited effects on the intake of standard chow or water (18), which suggests that the endocannabinoid system plays a role in the increased consumption of palatable substances. Similarly, Di Marzo and colleagues (15) reported that SR141716-treated mice and CB1–/– mice ate significantly less than did control mice following 18 hours of food deprivation. They also found that ob/ob and db/db mice and Zucker rats, genetic rodent models of obesity, possessed elevated levels of endocannabinoids in the hypothalamus compared with those in nonobese control mice, while no differences were found in other brain regions (e.g., the cerebellum). The observation that SR141716 decreases food intake in obese animals suggests that endocannabinoids in the hypothalamus may play a role in hyperphagic responses. Other evidence indicates that endocannabinoids are involved in the neural circuitry of feeding regulated by leptin, a hormone that plays a key role in modulating food intake and body fat. Whereas leptin-deficient mice become obese and exhibit increased levels of endogenous cannabinoids in the hypothalamus, administration of leptin leads to a decrease in feeding and a concomitant reduction of anandamide and 2-AG expression in the hypothalamus (15). Conversely, CB1–/– mice possess significantly decreased plasma levels of leptin and have reduced body fat, but exhibit enhanced sensitivity to exogenously administered leptin compared with that in wild-type mice (19, 20).
Cota and colleagues proposed that the endocannabinoid system plays a dual role in regulating body weight through a central orexigenic effect and in the regulation of peripheral lipogenesis (19). While stimulation of the endocannabinoid system can lead to increases in caloric consumption depending on the type of food available and whether the animal has been fasted, the number of calories consumed does not account for body weight differences found between SR141716-treated or CB1–/– animals and controls. Instead, several lines of evidence suggest a peripheral role for endocannabinoids in the regulation of lipogenesis and body weight in adult animals. SR141716 consistently alters hormone and serum lipid levels associated with animal models of obesity (21, 22). In addition, the cannabinoid receptor agonist WIN-55,212-2 stimulates lipogenesis in primary adipocyte cell cultures (19). The presence of CB1 mRNA in fat tissue from wild-type mice is consistent with a direct role of endocannabinoids in the regulation of lipogenesis.
CB1 activation of SREBP-1c in liver and hypothalamus
In this issue of the JCI, Osei-Hyiaman and colleagues identify the liver as a primary site responsible for endocannabinoid-mediated modulation of lipogenesis (23). Moreover, they present compelling evidence supporting a common molecular pathway for peripheral lipogenic and central appetite regulation by an endocannabinoid signaling system, which involves the lipogenic transcription factor SREBP-1c (Figure (Figure1)1) (24). Systemic administration of the potent cannabinoid receptor agonist HU210 led to significant increases in mRNA and protein levels of SREBP-1c, as well as those of its target enzymes, acetyl-CoA carboxylase-1 (ACC1) and fatty acid synthase (FAS), in liver. A functional consequence of the activation of these proteins was a 2-fold increase in the rate of fatty acid synthesis in liver, an effect that was blocked by SR141716 administration and did not occur in CB1–/– mice. HU210 also increased SREBP-1c and FAS mRNA levels in the hypothalamus through a CB1-mediated mechanism. Although SR141716 given alone failed to affect basal hypothalamic mRNA levels of SREBP-1c and FAS in both mice that had food available ad libitum and those that were food-deprived, it blocked the increase of both of these transcripts in mice that were given access to a high-carbohydrate diet following 24 hours of food deprivation. Regardless, the observation that CB1+/+ and CB1–/– mice had a similar total caloric intake, independent of diet, supports the assertion that increased cannabinoid-mediated lipogenesis plays a more dominant role in diet-induced obesity than does hyperphagia. In addition to calorie intake and lipogenesis, other factors such as resting metabolic rate, total energy expenditure, and dietary-induced thermogenesis play a critical role in regulating body weight. Presently, the relationship between endocannabinoids and methods of energy expenditure is largely unknown, and the possibility that endocannabinoids may modulate these processes cannot be negated.
A particularly provocative implication of the work by Osei-Hyiaman et al. (23) is that endocannabinoid-mediated modulation of lipogenesis in the liver may contribute to the development of fatty liver and obesity. Wild-type mice maintained on a high-fat diet gained significant amounts of weight, mostly in the form of adipose tissue, and had altered levels of enzymes associated with metabolism, including insulin, leptin, and adiponectin. Additionally, these mice had an increased rate of hepatic fatty acid synthesis, showed increased levels of triglycerides, and developed fatty liver. In contrast, CB1–/– mice maintained on a high-fat diet did not exhibit increases in fatty acid synthesis, exhibited serum hormone and lipid profiles similar to wild-type mice fed regular chow, and did not develop fatty liver. Similarly, SR141716 administration significantly attenuated the elevation in hepatic fatty acid synthesis in wild-type mice fed a high-fat diet. These findings are corroborated in other reports (25, 26), in which chronic SR141716 treatment of mice maintained on high-fat diets was found to have similar beneficial effects with respect to serum lipids, leptin, and body weight as those observed in CB1–/– mice.
Another important finding reported by Osei-Hyiaman et al. is that the endo-genous cannabinoid system in the liver undergoes adaptive changes in response to diet (23). Wild-type mice maintained on a high-fat diet developed fatty liver associated with significant increases in hepatic levels of CB1 and anandamide. Hepatic 2-AG levels were unaffected by diet, which suggests that anandamide is the predominant endocannabinoid signaling molecule in this liver pathway. The elevated levels of hepatic anandamide appear to be due to a decrease in activity of fatty acid amide hydrolase (FAAH), the primary enzyme responsible for anandamide catabolism in vivo (27). Curiously, the level of FAAH protein in liver was unaffected by diet, suggesting that the high-fat diet led to a decrease in anandamide degradation, possibly the result of the elevated levels of fatty acids and other endogenous factors competing for FAAH. In contrast, N-acyltransferase, an enzyme regulating anandamide synthesis (28), was unaffected.
Collectively, Osei-Hyiaman and colleagues have demonstrated that stimulation of CB1 in liver with HU210 leads to an increased rate of hepatic fatty acid synthesis through a mechanism involving increases in SREBP-1c and its target enzymes, ACC1 and FAS (23). Similarly, they report intriguing evidence that anandamide activation of CB1 in liver is necessary for increased fatty acid synthesis following consumption of a high-fat diet. According to this model, consumption of a diet high in fats would lead to increases in fatty acid synthesis through the upregulation of endocannabinoid-mediated SREBP-1c in liver. Future work will need to address the issue of whether conditions that elevate hepatic anandamide levels are sufficient to stimulate SREBP-1c, ACC1, and FAS. Increasing the storage of fat could conceivably be an adaptive advantage in situations in which food is scarce, but could contribute to obesity, along with decreases in energy expenditure, when high-fat diets are consumed on a regular basis. A similar pathway involving endocannabinoid modulation of SREBP-1c in the hypothalamus may account for increased feeding behavior following periods of food deprivation. Both pathways are likely to contribute to the purported therapeutic efficacy of CB1 antagonists for the treatment of obesity and hyperlipidemia. Nonetheless, the devastating impact that the disruption of CB1 signaling has on feeding and growth in young mice (19, 29) necessitates that caution should be applied for the use of this approach in pregnant women and nursing mothers. Conversely, stimulation of hepatic and hypothalamic endocannabinoid pathways may account for the efficacy of Δ9-THC in the treatment of wasting syndromes associated with AIDS and cancer.
Footnotes
See the related article beginning on page 1298.
Nonstandard abbreviations used: Δ9-THC; Δ9-tetrahydrocannabinol; 2-AG, 2-arachidonoylglycerol; ACC1, acetyl-CoA carboxylase-1; CB1, cannabinoid receptor 1; FAAH, fatty acid amidohydrolase; FAS, fatty acid synthase.
Conflict of interest: The authors have declared that no conflict of interest exists.
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