The conserved endocannabinoid anandamide modulates olfactory sensitivity to induce hedonic feeding in C. elegans
The ability of cannabis to increase food consumption has been known for centuries. In addition to producing hyperphagia, cannabinoids can amplify existing preferences for calorically dense, palatable food sources, a phenomenon called hedonic amplification of feeding. These effects result from the ac...
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Published in | Current biology Vol. 33; no. 9; pp. 1625 - 1639.e4 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
08.05.2023
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Abstract | The ability of cannabis to increase food consumption has been known for centuries. In addition to producing hyperphagia, cannabinoids can amplify existing preferences for calorically dense, palatable food sources, a phenomenon called hedonic amplification of feeding. These effects result from the action of plant-derived cannabinoids that mimic endogenous ligands called endocannabinoids. The high degree of conservation of cannabinoid signaling at the molecular level across the animal kingdom suggests hedonic feeding may also be widely conserved. Here, we show that exposure of Caenorhabditis elegans to anandamide, an endocannabinoid common to nematodes and mammals, shifts both appetitive and consummatory responses toward nutritionally superior food, an effect analogous to hedonic feeding. We find that anandamide’s effect on feeding requires the C. elegans cannabinoid receptor NPR-19 but can also be mediated by the human CB1 cannabinoid receptor, indicating functional conservation between the nematode and mammalian endocannabinoid systems for the regulation of food preferences. Furthermore, anandamide has reciprocal effects on appetitive and consummatory responses to food, increasing and decreasing responses to inferior and superior foods, respectively. Anandamide’s behavioral effects require the AWC chemosensory neurons, and anandamide renders these neurons more sensitive to superior foods and less sensitive to inferior foods, mirroring the reciprocal effects seen at the behavioral level. Our findings reveal a surprising degree of functional conservation in the effects of endocannabinoids on hedonic feeding across species and establish a new system to investigate the cellular and molecular basis of endocannabinoid system function in the regulation of food choice.
•AEA reciprocally alters consumption of high- and low-quality foods in C. elegans•Reciprocity is evident in both feeding rate and chemotaxis preference•Deletion of the native cannabinoid receptor npr-19 is rescued by the human CNR1 gene•AEA reciprocally alters olfactory neuron sensitivity to high- and low-quality foods
The ability of cannabis to stimulate appetite for highly palatable food in humans has been known for centuries. Levichev et al. show that exposure of the nematode C. elegans to an endogenous cannabinoid specifically increases consumption of favored food, revealing an unexpected degree of conservation in cannabinoid effects on appetite. |
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AbstractList | The ability of cannabis to increase food consumption has been known for centuries. In addition to producing hyperphagia, cannabinoids can amplify existing preferences for calorically dense, palatable food sources, a phenomenon called hedonic amplification of feeding. These effects result from the action of plant-derived cannabinoids that mimic endogenous ligands called endocannabinoids. The high degree of conservation of cannabinoid signaling at the molecular level across the animal kingdom suggests hedonic feeding may also be widely conserved. Here, we show that exposure of Caenorhabditis elegans to anandamide, an endocannabinoid common to nematodes and mammals, shifts both appetitive and consummatory responses toward nutritionally superior food, an effect analogous to hedonic feeding. We find that anandamide's effect on feeding requires the C. elegans cannabinoid receptor NPR-19 but can also be mediated by the human CB1 cannabinoid receptor, indicating functional conservation between the nematode and mammalian endocannabinoid systems for the regulation of food preferences. Furthermore, anandamide has reciprocal effects on appetitive and consummatory responses to food, increasing and decreasing responses to inferior and superior foods, respectively. Anandamide's behavioral effects require the AWC chemosensory neurons, and anandamide renders these neurons more sensitive to superior foods and less sensitive to inferior foods, mirroring the reciprocal effects seen at the behavioral level. Our findings reveal a surprising degree of functional conservation in the effects of endocannabinoids on hedonic feeding across species and establish a new system to investigate the cellular and molecular basis of endocannabinoid system function in the regulation of food choice. The ability of cannabis to increase food consumption has been known for centuries. In addition to producing hyperphagia, cannabinoids can amplify existing preferences for calorically dense, palatable food sources, a phenomenon called hedonic amplification of feeding. These effects result from the action of plant-derived cannabinoids that mimic endogenous ligands called endocannabinoids. The high degree of conservation of cannabinoid signaling at the molecular level across the animal kingdom suggests hedonic feeding may also be widely conserved. Here, we show that exposure of Caenorhabditis elegans to anandamide, an endocannabinoid common to nematodes and mammals, shifts both appetitive and consummatory responses toward nutritionally superior food, an effect analogous to hedonic feeding. We find that anandamide's effect on feeding requires the C. elegans cannabinoid receptor NPR-19 but can also be mediated by the human CB1 cannabinoid receptor, indicating functional conservation between the nematode and mammalian endocannabinoid systems for the regulation of food preferences. Furthermore, anandamide has reciprocal effects on appetitive and consummatory responses to food, increasing and decreasing responses to inferior and superior foods, respectively. Anandamide's behavioral effects require the AWC chemosensory neurons, and anandamide renders these neurons more sensitive to superior foods and less sensitive to inferior foods, mirroring the reciprocal effects seen at the behavioral level. Our findings reveal a surprising degree of functional conservation in the effects of endocannabinoids on hedonic feeding across species and establish a new system to investigate the cellular and molecular basis of endocannabinoid system function in the regulation of food choice. The ability of cannabis to increase food consumption has been known for centuries. In addition to producing hyperphagia, cannabinoids can amplify existing preferences for calorically dense, palatable food sources, a phenomenon called hedonic amplification of feeding. These effects result from the action of plant-derived cannabinoids that mimic endogenous ligands called endocannabinoids. The high degree of conservation of cannabinoid signaling at the molecular level across the animal kingdom suggests hedonic feeding may also be widely conserved. Here we show that exposure of C. elegans to anandamide, an endocannabinoid common to nematodes and mammals, shifts both appetitive and consummatory responses toward nutritionally superior food, an effect analogous to hedonic feeding. We find that anandamide’s effect on feeding requires the C. elegans cannabinoid receptor NPR-19 but can also be mediated by the human CB1 cannabinoid receptor, indicating functional conservation between the nematode and mammalian endocannabinoid systems for regulation of food preferences. Furthermore, anandamide has reciprocal effects on appetitive and consummatory responses to food, increasing and decreasing responses to inferior and superior food respectively. Anandamide’s behavioral effects require the AWC chemosensory neurons, and anandamide renders these neurons more sensitive to superior food and less sensitive to inferior food, mirroring the reciprocal effects seen at the behavioral level. Our findings reveal a surprising degree of functional conservation in the effects of endocannabinoids on hedonic feeding across species and establish a new system to investigate the cellular and molecular basis of endocannabinoid system function in the regulation of food choice. The ability of cannabis to stimulate appetite for highly palatable food in humans has been known for centuries. Levichev et al. show that exposure of the nematode C. elegans to an endogenous cannabinoid specifically increases consumption of favored food, revealing an unexpected degree of conservation in cannabinoid effects on appetite. The ability of cannabis to increase food consumption has been known for centuries. In addition to producing hyperphagia, cannabinoids can amplify existing preferences for calorically dense, palatable food sources, a phenomenon called hedonic amplification of feeding. These effects result from the action of plant-derived cannabinoids that mimic endogenous ligands called endocannabinoids. The high degree of conservation of cannabinoid signaling at the molecular level across the animal kingdom suggests hedonic feeding may also be widely conserved. Here, we show that exposure of Caenorhabditis elegans to anandamide, an endocannabinoid common to nematodes and mammals, shifts both appetitive and consummatory responses toward nutritionally superior food, an effect analogous to hedonic feeding. We find that anandamide’s effect on feeding requires the C. elegans cannabinoid receptor NPR-19 but can also be mediated by the human CB1 cannabinoid receptor, indicating functional conservation between the nematode and mammalian endocannabinoid systems for the regulation of food preferences. Furthermore, anandamide has reciprocal effects on appetitive and consummatory responses to food, increasing and decreasing responses to inferior and superior foods, respectively. Anandamide’s behavioral effects require the AWC chemosensory neurons, and anandamide renders these neurons more sensitive to superior foods and less sensitive to inferior foods, mirroring the reciprocal effects seen at the behavioral level. Our findings reveal a surprising degree of functional conservation in the effects of endocannabinoids on hedonic feeding across species and establish a new system to investigate the cellular and molecular basis of endocannabinoid system function in the regulation of food choice. •AEA reciprocally alters consumption of high- and low-quality foods in C. elegans•Reciprocity is evident in both feeding rate and chemotaxis preference•Deletion of the native cannabinoid receptor npr-19 is rescued by the human CNR1 gene•AEA reciprocally alters olfactory neuron sensitivity to high- and low-quality foods The ability of cannabis to stimulate appetite for highly palatable food in humans has been known for centuries. Levichev et al. show that exposure of the nematode C. elegans to an endogenous cannabinoid specifically increases consumption of favored food, revealing an unexpected degree of conservation in cannabinoid effects on appetite. |
Author | White, Amanda M. Purcell, Zhifeng Lockery, Shawn R. Chicas-Cruz, Kathy Faumont, Serge Levichev, Anastasia Berner, Rachel Z. |
AuthorAffiliation | 1 University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, Oregon, 97403, USA |
AuthorAffiliation_xml | – name: 1 University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, Oregon, 97403, USA |
Author_xml | – sequence: 1 givenname: Anastasia surname: Levichev fullname: Levichev, Anastasia organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA – sequence: 2 givenname: Serge surname: Faumont fullname: Faumont, Serge organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA – sequence: 3 givenname: Rachel Z. surname: Berner fullname: Berner, Rachel Z. organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA – sequence: 4 givenname: Zhifeng surname: Purcell fullname: Purcell, Zhifeng organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA – sequence: 5 givenname: Amanda M. surname: White fullname: White, Amanda M. organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA – sequence: 6 givenname: Kathy surname: Chicas-Cruz fullname: Chicas-Cruz, Kathy organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA – sequence: 7 givenname: Shawn R. orcidid: 0000-0001-8535-7989 surname: Lockery fullname: Lockery, Shawn R. email: shawn@uoregon.edu organization: University of Oregon, Institute of Neuroscience, 1245 University of Oregon, Eugene, OR 97403, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37084730$$D View this record in MEDLINE/PubMed |
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Keywords | NPR-19 CB1 chemosensation cannabinoids appetite palatable food AEA calcium imaging energy homeostasis munchies |
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Title | The conserved endocannabinoid anandamide modulates olfactory sensitivity to induce hedonic feeding in C. elegans |
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