Watkins Bruce A, Kim Jeffrey
Department of Nutrition, University of California Davis, Davis, CA, USA.
Division of Cardiovascular Medicine, Department of Internal Medicine, University of California Davis, Davis, CA, USA.
Front Psychol. 2015 Jan 6;5:1506. doi: 10.3389/fpsyg.2014.01506. eCollection 2014.
For many years, the brain has been the primary focus for research on eating behavior. More recently, the discovery of the endocannabinoids (EC) and the endocannabinoid system (ECS), as well as the characterization of its actions on appetite and metabolism, has provided greater insight on the brain and food intake. The purpose of this review is to explain the actions of EC in the brain and other organs as well as their precursor polyunsaturated fatty acids (PUFA) that are converted to these endogenous ligands. The binding of the EC to the cannabinoid receptors in the brain stimulates food intake, and the ECS participates in systemic macronutrient metabolism where the gastrointestinal system, liver, muscle, and adipose are involved. The EC are biosynthesized from two distinct families of dietary PUFA, namely the n-6 and n-3. Based on their biochemistry, these PUFA are well known to exert considerable physiological and health-promoting actions. However, little is known about how these different families of PUFA compete as precursor ligands of cannabinoid receptors to stimulate appetite or perhaps down-regulate the ECS to amend food intake and prevent or control obesity. The goal of this review is to assess the current available research on ECS and food intake, suggest research that may improve the complications associated with obesity and diabetes by dietary PUFA intervention, and further reveal mechanisms to elucidate the relationships between substrate for EC synthesis, ligand actions on receptors, and the physiological consequences of the ECS. Dietary PUFA are lifestyle factors that could potentially curb eating behavior, which may translate to changes in macronutrient metabolism, systemically and in muscle, benefiting health overall.
多年来,大脑一直是饮食行为研究的主要焦点。最近,内源性大麻素(EC)和内源性大麻素系统(ECS)的发现,以及其对食欲和新陈代谢作用的表征,为大脑与食物摄入提供了更深入的见解。本综述的目的是解释EC在大脑和其他器官中的作用,以及它们可转化为这些内源性配体的前体多不饱和脂肪酸(PUFA)。EC与大脑中的大麻素受体结合会刺激食物摄入,并且ECS参与全身常量营养素代谢,其中涉及胃肠道系统、肝脏、肌肉和脂肪组织。EC由两类不同的膳食PUFA生物合成,即n-6和n-3。基于它们的生物化学性质,这些PUFA以发挥相当大的生理和促进健康作用而闻名。然而,对于这些不同类别的PUFA如何作为大麻素受体的前体配体相互竞争以刺激食欲,或者下调ECS以改变食物摄入量并预防或控制肥胖,人们知之甚少。本综述的目标是评估目前关于ECS与食物摄入的现有研究,提出可能通过膳食PUFA干预改善与肥胖和糖尿病相关并发症的研究,并进一步揭示阐明EC合成底物、配体对受体的作用以及ECS生理后果之间关系的机制。膳食PUFA是可能抑制饮食行为的生活方式因素,这可能转化为常量营养素代谢在全身和肌肉中的变化,总体上有益于健康。