胰高血糖素样肽-1受体激动剂在肥胖和食物成瘾治疗中的作用机制
Mechanism of glucagon-like peptide-1 receptor agonist in the treatment of obesity and food addiction
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摘要: 肥胖和食物成瘾已经成为危害人民群众健康的重要因素,其交互作用加剧代谢异常及并发症风险。胰高血糖素样肽-1受体激动剂(GLP-1RA)已成为治疗肥胖和食物成瘾的有利选择,其治疗机制也逐渐成为研究的热点和重点。研究表明,GLP-1RA通过中枢与外周机制抑制食欲、延缓胃排空,并作用于中脑边缘多巴胺系统,减少伏隔核多巴胺释放,削弱高热量食物的奖赏效应,从而改善食物成瘾行为,进一步治疗肥胖。然而,GLP-1RA的胃肠道不良反应及潜在长期风险仍需谨慎管理。文章就GLP-1RA治疗肥胖以及食物成瘾的临床研究进展进行综述,为肥胖和食物成瘾的药物选择提供参考。Abstract: Obesity and food addiction have become major threats to public health, and their synergistic interactions exacerbate metabolic abnormalities and comorbidities. Glucagon-like peptide-1 receptor agonist (GLP-1RA) has emerged as a promising therapeutic option for these conditions, and their mechanism of action has become a major research focus. Evidence indicates that GLP-1RA suppress appetite and delay gastric emptying through central and peripheral pathways. Furthermore, they modulate mesolimbic dopamine system (MLDS), reduce the release of dopamine in the nucleus accumben, attenuate the rewarding effects of high-calorie foods and ameliorate addictive eating behaviors, thereby treating obesity. However, adverse gastrointestinal effects and potential long-term risks of GLP-1RA necessitate cautious clinical management. In this article, recent clinical advances in the application of GLP-1RA applications for the treatment of obesity and food addiction were reviewed, providing reference for drug selection for obesity and food addiction.
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