Cannabinoid type-1 receptors in CaMKII neurons drive impulsivity in pathological eating behavior

被引:0
作者
Martin-Garcia, Elena [1 ,2 ,3 ]
Domingo-Rodriguez, Laura [1 ,2 ]
Lutz, Beat [4 ,5 ]
Maldonado, Rafael [1 ,2 ,3 ]
de Azua, Inigo Ruiz [4 ,5 ]
机构
[1] Univ Pompeu Fabra, Dept Expt & Hlth Sci, Lab Neuropharmacol Neurophar, Barcelona 08003, Spain
[2] Univ Autonoma Barcelona, Dept Psychobiol & Methodol Hlth Sci, Bellaterra 08193, Spain
[3] Hosp del Mar Med Res Inst IMIM, Barcelona, Spain
[4] Leibniz Inst Resilience Res, D-55122 Mainz, Germany
[5] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Physiol Chem, D-55128 Mainz, Germany
来源
MOLECULAR METABOLISM | 2024年 / 92卷
基金
欧盟第七框架计划;
关键词
Endocannabinoid system; Cannabinoid type 1 receptor (CB1); Impulsivity; Feeding behavior; Obesity; Metabolic syndrome; Food addiction; FOOD ADDICTION; RISK-FACTORS; ENDOCANNABINOID SYSTEM; CARDIOMETABOLIC RISK; OVERWEIGHT PATIENTS; ENERGY-BALANCE; OBESE-PATIENTS; CB1; RECEPTOR; WEIGHT; RIMONABANT;
D O I
10.1016/j.molmet.2025.102096
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Overconsumption of palatable food and energy accumulation are evolutionary mechanisms of survival when food is scarce. These innate mechanisms becom detrimental in obesogenic environment promoting obesity and related comorbidities, including mood disorders. This study aims at elucidating the role of the endocannabinoid system in energy accumulation and hedonic feeding. Methods: We applied a genetic strategy to reconstitute cannabinoid type-1 receptor (CB1) expression at functional levels specifically in CaMKII+ neurons (CaMKII-CB1-RS) and adipocytes (Ati-CB1-RS), respectively, in a CB1 deficient background. Results: Rescued CB1 expression in CaMKII+ neurons, but not in adipocytes, promotes feeding behavior, leading to fasting-induced hyperphagia, increased motivation, and impulsivity to palatable food seeking. In a diet-induced obesity model, CB1 re-expression in CaMKII+ neurons, but not in adipocytes, compared to complete CB1 deficiency, was sufficient to largely restore weight gain, food intake without any effect on glucose intolerance associated with high-fat diet consumption. In a model of glucocorticoid-mediated metabolic syndrome, CaMKII-CB1-RS mice showed all metabolic alterations linked to the human metabolic syndrome except of glucose intolerance. In a binge-eating model mimicking human pathological feeding, CaMKII-CB1-RS mice showed increased seeking and compulsive behavior to palatable food, suggesting crucial roles in foraging and an enhanced susceptibility to addictive-like eating behaviors. Importantly, other contingent behaviors, including increased cognitive flexibility and reduced anxiety-like behaviors, but not depressive-like behaviors, were also observed. Conclusions: CB1 in CaMKII+ neurons is instrumental in feeding behavior and energy storage under physiological conditions. The exposure to risk factors (hypercaloric diet, glucocorticoid dysregulation) leads to obesity, metabolic syndrome, binge-eating and food addiction. (c) 2025 The Authors. Published by Elsevier GmbH. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:13
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