Cannabinoids have an important role in regulating feeding behaviors via cannabinoid receptors in mammals. Cannabinoids also exhibit potential therapeutic functions in Drosophila melanogaster, or fruit fly that lacks cannabinoid receptors. However, it remains unclear whether cannabinoids affect food consumption and metabolism in a cannabinoid receptors-independent manner in flies. In this study, we systematically investigated pharmacological functions of various cannabinoids in modulating food preference and consumption in flies. We show that flies display preferences for consuming cannabinoids, independent of two important sensory regulators Poxn and Orco. Interestingly, phyto- and endo- cannabinoids exhibit an inhibitory effect on food intake. Unexpectedly, the non-selective CB1 receptor antagonist AM251 attenuates the suppression of food intake by endocannabinoids. Moreover, the endocannabinoid anandamide (AEA) and its metabolite inhibit food intake and promote resistance to starvation, possibly through reduced lipid metabolism. Thus, this study has provided insights into a pharmacological role of cannabinoids in feeding behaviors using an adult Drosophila model.
Eating disorders including binge eating, and anorexia and bulimia nervosa, and obesity are characterized by abnormal eating behaviors and dysregulation of food intake. These have immense long-term consequences on physical health that could manifest to cardiovascular diseases, and on mental health that leads to both somatic and psychosocial complications1. With the increasing burden on the society and healthcare system, research in the past decade has focused its efforts on understanding the mechanisms underlying the regulation of food intake and control of body weight, and ultimately developing therapeutic drug treatments to curb these issues.
Cannabis sativa, also known as marijuana, a herbaceous plant belonging to the family Cannabaceae, has been known for its medicinal and recreational purposes for over 5000 years2,3. Recently, it has gained recognition as a valuable source of unique compounds with various potential therapeutic applications4,5,6,7. It has since been reported that more than 100 phytocannabinoids are isolated and characterized to have active interaction with the endocannabinoid system8. Amongst these phytocannabinoids, Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD) are the most well-studied. Being a psychoactive constituent of Cannabis sativa, the use of THC as a pharmacological therapy is therefore limited, which draws further attention towards non-psychoactive phytocannabinoids. The non-psychoactive constituent CBD has shown to possess protective properties in various diseases including seizure, cancer and food disorders9,10,11. As a neuroprotective agent, CBD has been successfully approved for treatment of epilepsy by the US Food and Drug Administration (FDA) in 2018. This has opened up avenues to further study the therapeutic values of other non-psychoactive phytocannabinoids including cannabidivarin (CBDV), cannabichromene (CBC) and cannabigerol (CBG)12. N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol (2-AG) are the most important endocannabinoids in the canonical endocannabinoid system, and many studies have documented their roles in mediating physiological processes, such as neuroinflammation, pain perception and metabolism, through binding to CB1/2 receptors in mammals6,11. In addition, numerous synthetic cannabinoids are constructed as agonists/antagonists of CB1/2 receptors, and further utilized to probe into the physiological functions of the endocannabinoid system13. Although CB1/2 receptors are known to modulate the effects of these cannabinoids, non-canonical G protein-coupled receptors (GPCRs), such as transient receptor potential vanilloid (TRPV) channels, peroxisome proliferator-activated receptor (PPAR), orphan GPCR GPR55 and 5-HT1A, have also been reported to be pharmacological targets of these cannabinoids in mediating various physiological functions11.
The fruit fly, Drosophila melanogaster, is an excellent model as a platform for screening new drugs and unraveling molecular mechanisms14. Due to its conserved genome and sophisticated genetic tools, it has been widely used to study biological processes and diseases, such as obesity, neurological disorders and longevity. Despite the lack of canonical cannabinoid CB1/2 receptors, various orthologs of endocannabinoid-metabolized enzymes and non-canonical receptors are well conserved in Drosophila15,16. The major endocannabinoids, namely AEA and 2-AG, are expressed at low levels in Drosophila larvae as reported by some labs17,18, although undetectable in other studies19,20. Nevertheless, the endocannabinoid-like signal lipid 2-linoleoyl glycerol (2-LG) is abundant in flies16,20. These raise the possibility that cannabinoids may impact on the physiology and behaviors of Drosophila. Interestingly, a few recent studies have highlighted potential therapeutic effects of cannabinoids in Drosophila for treating various human diseases including cardiovascular diseases, seizures and Parkinson’s disease despite the absence of a canonical cannabinoid-signaling pathway21,22,23. Inhalation of vaporized marijuana leads to an increase in cardiac contractility in adult flies21. Importantly, the neuroprotective effects of cannabinoids are evident with exogenous application of AEA and 2-AG conferring neuroprotection against seizures in multiple fly models22. Pharmacological treatment with the synthetic cannabinoid CP55940, a non-selective CB1/2 receptor agonist, prolongs survival and restores locomotor activity against paraquat toxicity in flies23. Thus, Drosophila is emerging as a valuable model to elucidate the functions and pathways mediated by cannabinoids in a CB1/2 receptors-independent manner. However, little is known on the role of cannabinoids in food intake and metabolism in Drosophila. Studies using rodent models of feeding disorders have demonstrated that treatment with endocannabinoids positively regulates food consumption24,25,26. In contrast, exogenous AEA and 2-AG significantly inhibit food intake in C. elegans27. With the discrepancy in findings using different models, more research is required to determine the role of cannabinoids in food intake.
Here, we report cannabinoid preference and its inhibitory impact on food intake in Drosophila. We show that adult flies have an innate ability to detect and develop a preference for food containing cannabinoids, independent of two sensory regulators Poxn and Orco. Surprisingly, treatment with phyto- and endo- cannabinoids leads to a decrease in food intake. Interestingly, endocannabinoid-induced suppression in food intake is attenuated by AM251, a non-selective CB1 antagonist. Furthermore, we show that the endocannabinoid AEA prolongs starvation resistance and reduces lipid metabolism. Overall, this is the first systematic study demonstrating cannabinoid preference and its impact on feeding behavior in Drosophila.
Flies prefer to consume food containing phytocannabinoids
The non-psychoactive phytocannabinoids are naturally occurring compounds derived from Cannabis sativa, and exert their biological effects via interaction with cannabinoid receptors or other G-protein coupled receptors28. To investigate any potential role of cannabinoids in food preference in adult flies, we took advantage of the two-choice CAFE assay29, in which flies are presented with cannabinoid food and proper control food in four capillaries (Fig. 1A). We first assessed whether flies display a preference for four phytocannabinoids, including CBD, CBDV, CBC and CBG. Flies were presented with various concentrations of CBD (0.01 mg/ml, 0.1 mg/ml or 1 mg/ml), CBDV, CBC or CBG (0.01 mg/ml or 0.1 mg/ml) in each CAFE assay. Statistical analysis shows that the flies did not exhibit obvious preference for food with the individual phytocannabinoids in the first 2 days (Fig. 1B–E). Interestingly, a significant preference for these phytocannabinoids was observed in the following two days. Flies showed the preference for consuming food with 0.1 mg/ml or 1 mg/ml CBD on day 3 and day 4, however, appeared to prefer 0.01 mg/ml CBD only on day 4 (Fig. 1B). These data indicate that flies possess an ability to detect CBD and develop a dose-dependent CBD preference over time. Likewise, food containing high concentration of CBDV (Fig. 1C), CBC (Fig. 1D) or CBG (Fig. 1E), was preferentially consumed by the flies on day 3 and day 4. Flies also displayed food preference to CBG at the lower concentration on day 4 (Fig. 1E), similar to CBD (Fig. 1B). Thus, these data indicate that flies can develop a delayed preference for phytocannabinoids in a dose-dependent manner.
Flies prefer to consume food with endocannabinoids and synthetic cannabinoids
We next extended the characterization of food preference to endocannabinoids and synthetic cannabinoids. Flies were presented with either of endocannabinoids, namely anandamide (AEA) and 2-arachidonoylglycerol (2-AG), at 0.01 mg/ml and 0.1 mg/ml (Fig. 2A,B). The preference indexes of food intake indicate a robust preference for food with a high concentration of AEA (Fig. 2A) and 2-AG (Fig. 2B), but not with the lower concentration. The strong preference for 2-AG was sustained throughout 4 days of feeding (Fig. 2B), whereas the preference for AEA remained consistent, albeit relatively lower, in the first 3 days (Fig. 2A). These data suggest that AEA accumulation may be harmful to the flies on day 4. Previous studies have reported the identification of the endocannabinoid-like signal lipid 2-LG, an evolutionary alternative to 2-AG in Drosophila16,20. Arachidonic acid (AA) supplement can promote the synthesis of 2-AG in Drosophila16. We also observed a weak but significant preference for food containing 2-LG only on day 3, in contrast to more robust preference for food with AA throughout the entire course of feeding (Fig. 2C).
With the detection of food preference for endocannabinoids in flies, we further assessed potential preference for synthetic cannabinoids. Flies exhibited a significant preference for food containing 0.5 mM CP55940 over 4 days (Fig. 2D), but not for another CB1/CB2 receptor agonist WIN55212-2 at the same concentration (Fig. 2D). Given the absence of CB1/2 receptors in the fly genome, the results suggest that these two synthetic cannabinoids might target distinct receptors in Drosophila. Furthermore, we also investigated potential effect on food preference for AM251 (0.5 mM) or AM630 (0.5 mM), two antagonists of CB1 and CB2 receptors, respectively. The consumption for AM251 or AM630-containing food remained similar to that for the control food throughout 4 days of feeding, despite a weak preference for AM630 on day 3 (Fig. 2E). Fatty acid amide hydrolase (FAAH), which is well conserved between mammals and Drosophila30, catabolizes AEA into AA and ethanolamine31. Treatment with PF3845, an inhibitor of mammalian FAAH, has also been shown to increase the endocannabinoids in fly hemolymph30. Flies displayed a significant preference for food with 0.5 mM PF3845, and the preference index remained relatively high throughout 4 days of feeding (Fig. 2F). Taken together, these findings indicate a general preference for both endocannabinoids (AEA and 2-AG) and synthetic cannabinoid CP55940 in flies.
Cannabinoid preference is independent of Poxn and Orco, two important sensory regulators in flies
To examine whether the preferential response to cannabinoids is due to sensory stimuli in flies, we examined possible involvement of gustatory and olfactory functions in food preference using taste mutants (poxn70–23 and poxnΔM22-B5) (Fig. 3A,B), and olfaction mutants (orco1 and orco2) (Fig. 3C,D), respectively. In comparison to the control w1118 flies, both poxn and orco homozygotes displayed similar preference for 1 mg/ml CBD and 0.5 mM CP55940 over 4 consecutive days of feeding, suggesting that the preference for cannabinoids in flies is modulated through a mechanism independent of two gustatory and olfactory regulators, Poxn and Orco, respectively.
An inhibitory effect of phytocannabinoids on food intake
The lack of gustatory and olfactory sensory inputs in influencing cannabinoid preference suggests a potential pharmacological effect of these compounds on metabolism in Drosophila. Phytocannabinoids have been shown to affect food intake, and can be developed as potential therapeutic agents for obesity treatment12. We next investigated if phytocannabinoids regulate food intake in flies. The consumption of normal food by flies was quantified for two consecutive days following two days of cannabinoid training (Fig. 4A). Pre-treatment of the flies with higher concentrations of CBD at 1 mg/ml and 2 mg/ml, but not with the low concentration at 0.1 mg/ml, significantly decreased the total food intake on both days (Fig. 4B). The movement ability of flies was assessed to examine whether the effect observed in food intake was due to a decline in locomotion. In the negative geotaxis assay, the treatment with high concentration of CBD did not impair the climbing ability of adult flies (Figure S1A), suggesting that decreased food intake by CBD treatment is not attributed to altered locomotion. However, food intake was significantly decreased only on day 2 following the treatment with 0.1 mg/ml CBC and CBDV (Fig. 4C). No or negligible effect was detectable upon CBG treatment in flies (Fig. 4C). Subtle effects of CBC, CBDV and CBG could be due to their lower feeding concentration. We were unable to further increase the feeding concentration, given the low concentration of commercially available stock solutions. During the first two days of training, the amounts of food containing phytocannabinoids or the respective control solutions consumed by the flies remained similar (Figure S2). These control experiments suggest that the decrease in food intake is not caused by altered food consumption during the initial cannabinoid training. Thus, our results indicate that phytocannabinoids elicit a functional effect on the regulation of food intake in flies.
Endocannabinoids inhibit food intake
Growing studies have reported that endocannabinoid signaling functions to enhance food intake through the activation of CB1 receptor in mammals25. However, the sequence homology analysis indicated that canonical CB1 receptor appears to be absent in Drosophila15,32. Cannabinoids might function in an alternative way in flies, for example, via non-canonical cannabinoid receptors. To explore whether the endocannabinoids regulate food consumption, flies were pre-treated with AEA and 2-AG at the concentration of 0.01, 0.1 and 0.5 mg/ml in the first two days prior to the measurement of food intake in the next two days (Fig. 4A). The pre-treatment with higher concentrations of AEA exhibited profound effects on food intake whereby consumption of normal food was significantly attenuated on both days (Fig. 5A). Consistently, a significant reduction in food intake was observed with 2-AG treatment at the higher concentrations (Fig. 5B). However, this effect was only observed on the first day following the pre-treatment. Strikingly, the amounts of food containing the higher concentrations of AEA or 2-AG consumed by flies were significantly lower as compared to those of the normal food (Figure S3A and S3B). As a control, the climbing ability was not affected by either AEA or 2-AG treatment (Figure S1B and S1C). Next, we attempted to determine the possible effect of 2-LG (0.01 and 0.1 mg/ml) on food intake. Similar to 2-AG treatment, flies consumed significantly less food with 2-LG at the higher concentration of 0.1 mg/ml as compared to the normal food (Figure S3C) during the initial training. The pre-treatment with higher concentration of 2-LG also significantly decreased food consumption in the next two days (Fig. 5C).
A recent study has reported that AA facilitates 2-AG synthesis by the fly ortholog of diacylglycerol lipase dDAGL16. Since both 2-AG and 2-LG account for the reduction of food intake, we postulated that treatment with AA in flies may also have an inhibitory role in food intake. In agreement with our hypothesis, a similar inhibitory effect on food consumption was observed upon AA treatment. Normal food consumed by flies treated with higher concentration of AA at 0.1 mg/ml was significantly reduced as compared to the control group (Fig. 5D). Similarly, food consumption was remarkably lower during the first 2 days of 0.1 mg/ml AA pre-treatment (Figure S3D), and the climbing ability was not affected by AA treatment (Figure S1D). Together, these results suggest that endocannabinoids, like phytocannabinoids, elicit an inhibitory effect on the regulation of food consumption.
AM251 attenuated the inhibitory effect of AEA on food intake
It has been documented that the activity and levels of AEA and other endocannabinoids are negatively regulated via at least two modes. First, AEA and other endocannabinoids are degraded by FAAH31,33. Second, fatty acid-binding protein (FABP) facilitates the transportation of AEA to FAAH, which leads to subsequent degradation and inactivation of AEA34. Overexpression of FABP significantly promotes AEA uptake and hydrolysis in neuroblastoma cells35. FABPs also negatively regulates other endocannabinoids, as mice lacking FABPs possess elevated levels of N-acylethanolamines36. Given that endocannabinoid treatment led to a reduction in food intake, we next examined whether changes in endogenous endocannabionoid levels through FAAH inhibition or FABP overexpression can affect food intake. Importantly, treatment with the FAAH inhibitor PF3845, which inhibits degradation of various endocannabinoids and leads to increases the levels of multiple ethanolamides in flies30, led to a significant reduction in food intake on day 1 (Fig. 6A). Likewise, food consumption was significantly reduced during PF3845 pre-treatment (Figure S3E). Conversely, overexpression of fly dFABP, which may downregulate various endocannabinoids in flies, significantly enhanced the food intake on two consecutive days (Fig. 6B). These results are in line with an inhibitory effect of endocannabinoids on food intake.
Next, we sought to determine whether the CB1 receptor antagonist AM251 (0.5 mM) can counteract AEA (0.1 mg/ml) or 2-AG (0.1 mg/ml) effect in terms of food intake. Flies pre-fed with AM251 did not alter the levels of food intake in the following two days (Fig. 6C). Flies also consumed similar amount of food containing AM251 during the pre-treatment (Figure S3F). These results indicate that the treatment with this CB1 receptor antagonist did not affect food consumption in flies. Treatment with 0.1 mg/ml AEA or 2-AG led to significant reductions in normal food consumption (Fig. 6D,E). Interestingly, co-treatment of AM251 with AEA (Fig. 6D) or 2-AG (Fig. 6E) significantly attenuated their inhibitory effects on food intake. Due to the lack of canonical CB1/2 receptors in Drosophila genome, AEA and 2-AG regulate food intake, likely via another unknown receptor that can be blocked by AM251.
AEA treatment promotes starvation resistance and inhibits lipid metabolism
Given that phyto- and endo- cannabinoids can modulate food intake in flies, we next tested whether they also affect starvation resistance and lipid metabolism. Starvation resistance was quantified by measuring the survival percentage of the flies following cannabinoid treatment. After treatment with 0.1 mg/ml AEA, 0.1 mg/ml AA or 0.5 mM CP55940 for 2 days, flies exhibited significant increases in the survival rate (Fig. 7A,C,E), suggesting an enhanced resistance to starvation. Unexpectedly, neither 2-AG nor CBD pre-treatment showed any effect on starvation resistance (Fig. 7B,D). The observation of enhanced starvation resistance further prompted us to investigate whether body fat deposition was affected by AEA. Following 18 h starvation, the levels of triglyceride (TAG) were measured in endocannabinoid-treated flies. TAG levels in AEA- or AA- treated flies were significantly elevated when compared to the control flies (Fig. 7F). In line with no effect on starvation resistance, we did not observe a significant alteration in TAG levels upon 2-AG treatment (Fig. 7F). Thus, AEA and AA can enhance the resistance to starvation likely through the inhibition of lipid metabolism.
Drosophila has been developed as an important invertebrate model for drug screening due to its conserved genome and biological machineries. In this study, we utilized this model to investigate the effects of a spectrum of cannabinoids including phytocannabinoids, endocannabinoids and synthetic cannabinoids on food preference and consumption. Our findings reveal cannabinoid preference as well as an inhibitory function of cannabinoids in food intake in flies. As canonical CB1/2 receptors are absent in flies, this study provides insight into the pharmacological role of cannabinoids in the modulation of food consumption via a non-canonical cannabinoid signaling pathway.
Cannabis extracts are known to possess pesticidal properties, which can effectively repel insects and inhibit the growth of microbial pathogens37. While the naturally occurring phytocannabinoids display potential pharmacological roles, it is still poorly understood whether Drosophila is a useful model for understanding the functions of phytocannabinoids. Here, we characterize the preference for consuming cannabinoids in flies by using the two-choice feeding assay. The results indicate that flies display a significant preference for phytocannabinoids over time. A recent study has showed that Tobacco Hornworm Manduca sexta larvae prefer the food with low concentration of CBD over higher dose of CBD, and high CBD concentration is detrimental for larvae development38. However, no aversive response to phytocannabinoids was detected in this study. One possibility is that relatively low concentrations of phytocannabinoids were administrated in our CAFE assays. While we also observed a delayed development of fly larvae upon CBD treatment (data not shown), our current findings indicate these phytocannabinoids are not toxic to adult flies, at least at the relatively low concentrations used in this study.
In contrast to phytocannabinoids, flies displayed quicker and stronger preference for endocannabinoids and psychoactive cannabinoid CP55940. Although endocannabinoids are present in various vertebrates, very low amount of AEA and 2-AG is produced in flies17,18. AA, a critical substrate for eicosanoid biosynthesis, is also almost undetectable in flies39. A previous behavioral study in Drosophila has revealed a stage-specific discrimination of fatty acids. Larvae prefer various unsaturated fatty acids, but adult flies develop a preference for the diet containing high saturated fatty acids40. In this present study, we found that no apparent toxicity and aversive responses to these cannabinoids were detectable in flies, consistently, two important sensory regulators of gustatory and olfactory systems did not influence cannabinoid preference. These findings suggest that the cannabinoids may have some pharmacological roles in Drosophila. Several previous studies have highlighted the protective effects of the endocannabinoids and the synthetic cannabinoid CP55940 through non-canonical signaling pathways in Drosophila. Endocannabinoids and their metabolite AA were shown to possess anti-convulsant properties in protecting against seizures through the TRP channel Water witch in fly seizure models22; CP55940 alleviates paraquat-induced toxicity with the observations of increased survival and locomotion via the JNK signaling pathway23. Thus, our studies and others suggest that Drosophila may be an alternative model to dissect CB1/2 receptors-independent roles of cannabinoids as well as their pharmacological functions in diseases.
To understand whether cannabinoids affect food intake and metabolism, we systematically characterized the effects of various available cannabinoids in flies. The food intake was found to significantly decrease following pre-treatment with CBD, which is consistent with previous mammalian studies illustrating the effectiveness of CBD in controlling food consumption and preventing obesity in rodents11,41,42. Although these results in both mammals and flies are seemingly similar, the underlying mechanisms apparently differ. CBD inhibits food intake by blocking CB1 receptor and activating CB2 receptor in rodents11. By contrast, in flies lacking CB1/2 receptors, CBD functions through a CB1/2 receptor-independent mechanism. Our study is the first to illustrate the pharmacological function of CBDV and CBC whereby they can reduce food consumption. However, CBG does not seem to affect the food intake in Drosophila, whereas in rats CBG promotes food consumption at a high concentration43. The lack of CBG effect on food intake in flies could be due to the administration of CBG at a lower concentration in this study. Overall, these phytocannabinoids did not display a strong phenotype, thus, their potential as a treatment for eating disorders requires further interrogations. Although phytocannabinoids can bind to CB1/2 receptors, they display higher affinity for other GPCRs, such as GPR55, TPRV channels and PPARγ44,45. Since these non-canonical cannabinoid receptors are well conserved, it is conceivable that phytocannabinoids may exert their protective roles through modulation of these receptors in flies. Thus, further studies are required to investigate whether and how phytocannabinoids regulate food intake via one of these GPCRs.
Similar to the actions of phytocannabinoids, the present study puts forward the idea that the endocannabinoid-mediated pathway may modulate food intake. Pre-treatment with AEA and 2-AG significantly inhibited the food intake in adult flies, which is consistent with the finding in C. elegans27. However, administration of AEA and 2-AG promotes food intake and increase odor detection via binding to CB1 receptor in rodents26,46. As there is a lack of cannabinoid receptors to transduce AEA and 2-AG signals in Drosophila15,32, they may function through pathways central to other lipids of N-acyl amides and 2-acyl glycerols. Although endocannabinoid-mediated downstream pathway in food intake remains to be determined, our findings reveal that 2-LG, a closely-related 2-acyl glycerol ligand, also shows inhibition of food intake, suggesting a possible existence of a signaling pathway for the regulation of food intake in Drosophila. Furthermore, previous studies have also reported that OEA reduced food intake in rodents and goldfish47,48. Both OEA and AEA belong to a family of fatty acid ethanolamides (FAEs). It is conceivable that endocannabioids in Drosophila regulates food intake via a mechanism, likely similar to other lipids of N-acyl amides and 2-acyl glycerols. Moreover, we also found that flies pre-treated with FAAH inhibitor PF3845 consumed less food, whereas overexpressing dFABP in flies increased the food intake. These data suggest that FAAH-induced AEA metabolism and FABP-mediated AEA inactivation are important for this feeding behavior, thus reinforcing the crucial role of AEA in regulating food intake. Interestingly, the CB1 receptor antagonist, AM251, counteracts the inhibitory effects of AEA and 2-AG on food intake. This could possibly be due to the interaction of endocannabinoids with known non-CB receptors or other unidentified CB1-like receptors which can be targeted by AM251. In addition to its primary role as a CB1/2 receptor antagonist, AM251 is found to facilitate the activation of GPR55 that is a known target of AEA and AA49,50. From our findings, we speculate that AEA and 2-AG might regulate food intake via a GPR55 ortholog in Drosophila. To date, no fly GPR55 ortholog has been characterized. Further work is required to identify a possible GPR55 ortholog and its implications in food intake in flies.
The inhibitory role of cannabinoids in food preference and intake is particularly interesting as there is an absence of CB1/2 receptors in Drosophila. First, phytocannabinoids have been shown to exhibit high affinity for various non-CB1/2 receptors, such as GPR55, TPR channels and PPARγ44,45, whereas the binding affinity to non-CB1/2 receptors is comparatively lower than CB1/2 receptors for endocannabinoids11. The extent of cannabinoid preference and cannabinoid-induced inhibition of food intake could be due to differential binding affinities to the receptors in flies. It is known that the structure of these cannabinoids determines its functional activity through the binding affinity to the CB1/2 receptors51. However, it is unknown how the structural element can affect the binding state of these cannabinoids to the non-canonical receptors. Second, the inhibitory effect of AEA and its metabolite AA could possibly be due to the decrease in lipid metabolism. It is very likely that the increase in TAG levels could underlie the enhancement of starvation resistance. Although 2-AG exhibited a similar outcome in food intake to AEA, it is surprising that 2-AG did not affect lipid metabolism. Possible mechanism of AEA action in lipid metabolism awaits future investigations.
In conclusion, our study demonstrates that adult flies can detect and develop the preference for phyto-, endo- and synthetic cannabinoids. Importantly, these cannabinoids can inhibit food intake. We show that the endocannabinoids (AEA and 2-AG) inhibit the food intake via an AM251-targeted pathway. Moreover, the endocannabinoid AEA modulates food intake and starvation resistance probably through low lipid metabolism.
Fly stocks and maintenance
The following fly stocks were obtained from Bloomington Drosophila stock center (BDSC; Indiana, USA): Canton S (#64349), w1118 (#5905), orco1 (#23129), orco2 (#23130), and poxn70–23 (#60688). The following fly stocks were kindly provided: poxnΔM22-B5 (M. Noll from University of Zurich, Switzerland)52, w1118 (isoCJ1) and dFABP (J.C.P. Yin from University of Wisconscin-Madison, USA)53. Flies were reared on standard medium at 25 °C and approximately 70% humidity under a 12 h light/12 h dark cycle. 3–5-day-old adult male flies were collected using light CO2 anesthesia and allowed to recover for 2 days before further experimentation.
Drug selection and delivery
Various cannabinoids used in this study were categorized into 1) phytocannabinoids, 2) endocannabinoids, and 3) synthetic cannabinoids (Table 1). These drugs were dissolved in their respective solvents and further diluted to the desired concentrations in liquid food (5% sucrose and 5% yeast extract).
For both food preference and food intake assays, flies were placed into feeding chambers, and presented with drug-containing liquid food (5% sucrose, 5% yeast extract) and the respective control food in the glass capillaries, as described below. All the experiments were performed at least three times.
Cannabinoid preference assay
The food preference was measured using the Capillary Feeder (CAFE) assay (Fig. 1A), as described in the previous studies54,55. Briefly, eight male flies (3–5 days old) were distributed into each vial containing 1% agarose at the bottom. Four 5 μl glass capillaries (VWR, USA) were inserted into the vial from the lid. Two capillaries were filled with normal control liquid food and the rest with cannabinoid-containing liquid food. The amount of liquid food in the capillaries was measured per day and replaced with fresh food daily for four consecutive days. Two parallel vials void of flies were used as controls in each assay to determine the extent of liquid evaporation from the glass capillaries. The mean amount of evaporation was subtracted from the values obtained for food consumption by the flies. The preference index was calculated as the (consumption of cannabinoid food − consumption of normal control food)/total consumption.
Total food consumption
For the assessment of food intake, the behavioral setup was similar to that in the cannabinoid preference assay with the exception that all four glass capillaries (VWR, USA) contained either control food or cannabinoid food in the first 2 days and normal liquid food in the subsequent two days. The total food consumption (μl/fly) was calculated as (food consumption − evaporation loss)/number of flies.
Locomotive activity assay
The locomotion of the flies was assessed using an automated climbing assay, as previously described56. Following treatment with cannabinoids for two days, flies were transferred into the climbing vials and were acclimatized for 5 min before testing them. Flies were allowed to climb up the walls of the vials before tapping them down to the bottom at 1-min intervals and this was repeated five times. The testing session was videotaped for analysis and the average climbing height of each fly in the first 6 s of the assay was recorded to determine the locomotive behavior of the flies.
Starvation resistance assay
Flies pre-treated with cannabinoids for two consecutive days were used to examine starvation resistance. The resistance to starvation was measured as the survival rate of the flies. Ten male flies were placed into each vial containing 1% agarose to prevent desiccation and were monitored at 25 °C and 70% humidity under the 12 h light/ 12 h dark cycle. The number of dead flies was counted every 6–12 h.
The levels of triacylglycerol (TAG) were measured in flies according to a previous study57. Following treatment of cannabinoids for two consecutive days, 10 adult male flies per vial were starved for 18 h. These flies were subsequently homogenized in 100 µl of PBS + 1% Triton-X and immediately heated at 70 °C for 10 min to inactivate lipases. 20 µl heat-treated homogenates were incubated with the same amount of triglyceride reagent (T2449; Sigma, UAS) or PBST at 37 °C for 60 min. 30 µl of each sample were subsequently added to 100 µl free glycerol reagent (F6428; Sigma, USA) in a clear 96-well plate and incubated for 5 min at 37 °C. The absorbance of the samples was assayed using a multimode microplate reader at 540 nm. TAG concentration was determined by subtracting the absorbance for the free glycerol in the untreated samples from the total glycerol concentration in samples that were incubated with the triglyceride reagent. The levels of TAG were calculated based on the triolein-equivalent standard curve. TAG assay was repeated 3–4 times.
Statistical analysis was performed with Prism 7.03 (GraphPad Software, USA). Statistical significance was established using Student’s t test or one-way ANOVA followed by Dunnett’s post-hoc test in the cannabinoid preference and food intake assays, and Log-rank (Mantel-Cox) test in the starvation resistance assays. Differences between treatment groups were considered to be statistically significant at *p < 0.05, **p < 0.01, ***p < 0.001. The data were expressed as mean ± standard error of mean (S.E.M).
Himmerich, H., Kan, C., Au, K. & Treasure, J. Pharmacological treatment of eating disorders, comorbid mental health problems, malnutrition and physical health consequences. Pharmacol. Therap. https://doi.org/10.1016/j.pharmthera.2020.107667 (2020).
Volkow, N. D., Compton, W. M. & Weiss, S. R. Adverse health effects of marijuana use. N. Engl. J. Med. 371, 879. https://doi.org/10.1056/NEJMc1407928 (2014).
Andre, C. M., Hausman, J. F. & Guerriero, G. Cannabis sativa: The plant of the thousand and one molecules. Front. Plant Sci. 7, 19. https://doi.org/10.3389/fpls.2016.00019 (2016).
Baker, D., Pryce, G., Giovannoni, G. & Thompson, A. J. The therapeutic potential of cannabis. Lancet Neurol. 2, 291–298. https://doi.org/10.1016/s1474-4422(03)00381-8 (2003).
Lambert, D. M. & Fowler, C. J. The endocannabinoid system: drug targets, lead compounds, and potential therapeutic applications. J. Med. Chem. 48, 5059–5087. https://doi.org/10.1021/jm058183t (2005).
Maccarrone, M., Guzmán, M., Mackie, K., Doherty, P. & Harkany, T. Programming of neural cells by (endo)cannabinoids: from physiological rules to emerging therapies. Nat. Rev. Neurosci. 15, 786–801. https://doi.org/10.1038/nrn3846 (2014).
Jett, J., Stone, E., Warren, G. & Cummings, K. M. Cannabis use, lung cancer, and related issues. J. Thorac. Oncol. 13, 480–487. https://doi.org/10.1016/j.jtho.2017.12.013 (2018).
ElSohly, M. & Gul, W. Constituents of Cannabis Sativa. Handb. Cannabis https://doi.org/10.1093/acprof:oso/9780199662685.003.0001 (2015).
Devinsky, O. et al. Effect of cannabidiol on drop seizures in the Lennox–Gastaut syndrome. N. Engl. J. Med. 378, 1888–1897. https://doi.org/10.1056/NEJMoa1714631 (2018).
Jeong, S. et al. Cannabidiol-induced apoptosis is mediated by activation of Noxa in human colorectal cancer cells. Cancer Lett. 447, 12–23. https://doi.org/10.1016/j.canlet.2019.01.011 (2019).
Cristino, L., Bisogno, T. & Di Marzo, V. Cannabinoids and the expanded endocannabinoid system in neurological disorders. Nat. Rev. Neurol. 16, 9–29. https://doi.org/10.1038/s41582-019-0284-z (2020).
Bielawiec, P., Harasim-Symbor, E. & Chabowski, A. Phytocannabinoids: Useful drugs for the treatment of obesity? Special focus on cannabidiol. Front. Endocrinol. 11, 114. https://doi.org/10.3389/fendo.2020.00114 (2020).
Diao, X. & Huestis, M. A. New synthetic cannabinoids metabolism and strategies to best identify optimal marker metabolites. Front. Chem. 7, 109. https://doi.org/10.3389/fchem.2019.00109 (2019).
Pandey, U. B. & Nichols, C. D. Human disease models in Drosophila melanogaster and the role of the fly in therapeutic drug discovery. Pharmacol. Rev. 63, 411–436. https://doi.org/10.1124/pr.110.003293 (2011).
McPartland, J. M., Matias, I., Di Marzo, V. & Glass, M. Evolutionary origins of the endocannabinoid system. Gene 370, 64–74. https://doi.org/10.1016/j.gene.2005.11.004 (2006).
Tortoriello, G. et al. Genetic manipulation of sn-1-diacylglycerol lipase and CB1 cannabinoid receptor gain-of-function uncover neuronal 2-linoleoyl glycerol signaling in Drosophila melanogaster. Cannabis Cannabinoid Res. https://doi.org/10.1089/can.2020.0010 (2020).
Jeffries, K. A., Dempsey, D. R., Behari, A. L., Anderson, R. L. & Merkler, D. J. Drosophila melanogaster as a model system to study long-chain fatty acid amide metabolism. FEBS Lett. 588, 1596–1602. https://doi.org/10.1016/j.febslet.2014.02.051 (2014).
McPartland, J., Di Marzo, V., De Petrocellis, L., Mercer, A. & Glass, M. Cannabinoid receptors are absent in insects. J. Comp. Neurol. 436, 423–429. https://doi.org/10.1002/cne.1078 (2001).
Shen, L. R. et al. Drosophila lacks C20 and C22 PUFAs. J. Lipid Res. 51, 2985–2992. https://doi.org/10.1194/jlr.M008524 (2010).
Tortoriello, G. et al. Targeted lipidomics in Drosophila melanogaster identifies novel 2-monoacylglycerols and N-acyl amides. PLoS ONE 8, e67865. https://doi.org/10.1371/journal.pone.0067865 (2013).
Gómez, I. M. et al. Inhalation of marijuana affects Drosophila heart function. Biology Open. https://doi.org/10.1242/bio.044081 (2019).
Jacobs, J. A. & Sehgal, A. Anandamide metabolites protect against seizures through the TRP channel water witch in Drosophila melanogaster. Cell Rep. 31, 107710. https://doi.org/10.1016/j.celrep.2020.107710 (2020).
Jimenez-Del-Rio, M., Daza-Restrepo, A. & Velez-Pardo, C. The cannabinoid CP55,940 prolongs survival and improves locomotor activity in Drosophila melanogaster against paraquat: Implications in Parkinson’s disease. Neurosci. Res. 61, 404–411. https://doi.org/10.1016/j.neures.2008.04.011 (2008).
Cardinal, P. et al. Hypothalamic CB1 cannabinoid receptors regulate energy balance in mice. Endocrinology 153, 4136–4143. https://doi.org/10.1210/en.2012-1405 (2012).
Koch, M. Cannabinoid receptor signaling in central regulation of feeding behavior: A mini-review. Front. Neurosci. 11, 293. https://doi.org/10.3389/fnins.2017.00293 (2017).
Soria-Gómez, E. et al. The endocannabinoid system controls food intake via olfactory processes. Nat. Neurosci. 17, 407–415. https://doi.org/10.1038/nn.3647 (2014).
Oakes, M. D., Law, W. J., Clark, T., Bamber, B. A. & Komuniecki, R. Cannabinoids activate monoaminergic signaling to modulate key C. elegans behaviors. J. Neurosci. 37, 2859–2869. https://doi.org/10.1523/jneurosci.3151-16.2017 (2017).
Morales, P., Hurst, D. P. & Reggio, P. H. Molecular targets of the phytocannabinoids: A complex picture. Prog. Chem. Org. Nat. Prod. 103, 103–131. https://doi.org/10.1007/978-3-319-45541-9_4 (2017).
Diegelmann, S. et al. The capillary feeder assay measures food intake in Drosophila melanogaster. J. Vis. Exp. https://doi.org/10.3791/55024 (2017).
Khaliullina, H., Bilgin, M., Sampaio, J. L., Shevchenko, A. & Eaton, S. Endocannabinoids are conserved inhibitors of the Hedgehog pathway. Proc. Natl. Acad. Sci. USA 112, 3415–3420. https://doi.org/10.1073/pnas.1416463112 (2015).
Cravatt, B. F. et al. Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides. Nature 384, 83–87. https://doi.org/10.1038/384083a0 (1996).
McPartland, J. M. Phylogenomic and chemotaxonomic analysis of the endocannabinoid system. Brain Res. Brain Res. Rev. 45, 18–29. https://doi.org/10.1016/j.brainresrev.2003.11.005 (2004).
Mulder, A. M. & Cravatt, B. F. Endocannabinoid metabolism in the absence of fatty acid amide hydrolase (FAAH): Discovery of phosphorylcholine derivatives of N-acyl ethanolamines. Biochemistry 45, 11267–11277. https://doi.org/10.1021/bi061122s (2006).
Kaczocha, M., Vivieca, S., Sun, J., Glaser, S. T. & Deutsch, D. G. Fatty acid-binding proteins transport N-acylethanolamines to nuclear receptors and are targets of endocannabinoid transport inhibitors. J. Biol. Chem. 287, 3415–3424. https://doi.org/10.1074/jbc.M111.304907 (2012).
Kaczocha, M., Glaser, S. T. & Deutsch, D. G. Identification of intracellular carriers for the endocannabinoid anandamide. Proc. Natl. Acad. Sci. USA 106, 6375–6380. https://doi.org/10.1073/pnas.0901515106 (2009).
Kaczocha, M. et al. Fatty acid binding protein deletion suppresses inflammatory pain through endocannabinoid/N-acylethanolamine-dependent mechanisms. Mol. Pain 11, 52. https://doi.org/10.1186/s12990-015-0056-8 (2015).
Benelli, G. et al. The crop-residue of fiber hemp cv. Futura 75: From a waste product to a source of botanical insecticides. Environ. Sci. Pollut. Res. Int. 25, 10515–10525. https://doi.org/10.1007/s11356-017-0635-5 (2018).
Park, S. H. et al. Contrasting roles of cannabidiol as an insecticide and rescuing agent for ethanol-induced death in the tobacco hornworm Manduca sexta. Sci. Rep. 9, 10481. https://doi.org/10.1038/s41598-019-47017-7 (2019).
Burgoyne, R. D. & Morgan, A. The control of free arachidonic acid levels. Trends Biochem. Sci. 15, 365–366. https://doi.org/10.1016/0968-0004(90)90227-3 (1990).
Fougeron, A. S., Farine, J. P., Flaven-Pouchon, J., Everaerts, C. & Ferveur, J. F. Fatty-acid preference changes during development in Drosophila melanogaster. PLoS ONE 6, e26899. https://doi.org/10.1371/journal.pone.0026899 (2011).
Farrimond, J. A., Whalley, B. J. & Williams, C. M. Cannabinol and cannabidiol exert opposing effects on rat feeding patterns. Psychopharmacology 223, 117–129. https://doi.org/10.1007/s00213-012-2697-x (2012).
Wierucka-Rybak, M., Wolak, M. & Bojanowska, E. The effects of leptin in combination with a cannabinoid receptor 1 antagonist, AM 251, or cannabidiol on food intake and body weight in rats fed a high-fat or a free-choice high sugar diet. J Physiol. Pharmacol. 65, 487–496 (2014).
Brierley, D. I., Samuels, J., Duncan, M., Whalley, B. J. & Williams, C. M. Cannabigerol is a novel, well-tolerated appetite stimulant in pre-satiated rats. Psychopharmacology 233, 3603–3613. https://doi.org/10.1007/s00213-016-4397-4 (2016).
De Petrocellis, L. et al. Effects of cannabinoids and cannabinoid-enriched Cannabis extracts on TRP channels and endocannabinoid metabolic enzymes. Br. J. Pharmacol. 163, 1479–1494. https://doi.org/10.1111/j.1476-5381.2010.01166.x (2011).
Hill, T. D. et al. Cannabidivarin-rich cannabis extracts are anticonvulsant in mouse and rat via a CB1 receptor-independent mechanism. Br. J. Pharmacol. 170, 679–692. https://doi.org/10.1111/bph.12321 (2013).
Farrimond, J. A., Mercier, M. S., Whalley, B. J. & Williams, C. M. Cannabis sativa and the endogenous cannabinoid system: therapeutic potential for appetite regulation. Phytother. Res. 25, 170–188. https://doi.org/10.1002/ptr.3375 (2011).
Nielsen, M. J., Petersen, G., Astrup, A. & Hansen, H. S. Food intake is inhibited by oral oleoylethanolamide. J. Lipid Res. 45, 1027–1029. https://doi.org/10.1194/jlr.C300008-JLR200 (2004).
Tinoco, A. B. et al. Role of oleoylethanolamide as a feeding regulator in goldfish. J. Exp. Biol. 217, 2761–2769. https://doi.org/10.1242/jeb.106161 (2014).
Sharir, H. & Abood, M. E. Pharmacological characterization of GPR55, a putative cannabinoid receptor. Pharmacol. Ther. 126, 301–313. https://doi.org/10.1016/j.pharmthera.2010.02.004 (2010).
Ryberg, E. et al. The orphan receptor GPR55 is a novel cannabinoid receptor. Br. J. Pharmacol. 152, 1092–1101. https://doi.org/10.1038/sj.bjp.0707460 (2007).
Bow, E. W. & Rimoldi, J. M. The structure-function relationships of classical cannabinoids: CB1/CB2 modulation. Perspect. Med. Chem. https://doi.org/10.4137/pmc.s32171 (2016).
Boll, W. & Noll, M. The Drosophila Pox neuro gene: Control of male courtship behavior and fertility as revealed by a complete dissection of all enhancers. Development (Cambridge, England) 129, 5667–5681. https://doi.org/10.1242/dev.00157 (2002).
Gerstner, J. R., Vanderheyden, W. M., Shaw, P. J., Landry, C. F. & Yin, J. C. Fatty-acid binding proteins modulate sleep and enhance long-term memory consolidation in Drosophila. PLoS ONE 6, e15890. https://doi.org/10.1371/journal.pone.0015890 (2011).
Ja, W. W. et al. Prandiology of Drosophila and the CAFE assay. Proc. Natl. Acad. Sci. 104, 8253–8256. https://doi.org/10.1073/pnas.0702726104 (2007).
Devineni, A. V. & Heberlein, U. Preferential ethanol consumption in Drosophila models features of addiction. Curr. Biol. CB 19, 2126–2132. https://doi.org/10.1016/j.cub.2009.10.070 (2009).
Liu, H. et al. Automated rapid iterative negative geotaxis assay and its use in a genetic screen for modifiers of Aβ(42)-induced locomotor decline in Drosophila. Neurosci. Bull. 31, 541–549. https://doi.org/10.1007/s12264-014-1526-0 (2015).
Tennessen, J. M., Barry, W. E., Cox, J. & Thummel, C. S. Methods for studying metabolism in Drosophila. Methods 68, 105–115. https://doi.org/10.1016/j.ymeth.2014.02.034 (2014).
We thank M. Noll, J.C.P. Yin, and the Bloomington Stock Center (BSC) for generously providing fly stocks. We thank Dr. Shao Qin Yao for grant application and discussion, as well as the Yu lab members for helpful discussion.
This work was funded by Temasek Life Sciences Laboratory Singapore (TLL-2040) and National Research Foundation Singapore (SBP-P3 and SBP-P8) (both to F.Y.).
The authors declare no competing interests.
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He, J., Tan, A.M.X., Ng, S.Y. et al. Cannabinoids modulate food preference and consumption in Drosophila melanogaster. Sci Rep 11, 4709 (2021). https://doi.org/10.1038/s41598-021-84180-2
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