Bernecker Miriam, Lin Anna, Feuchtinger Annette, Molenaar Anna, Schriever Sonja C, Pfluger Paul T
Research Unit NeuroBiology of Diabetes, Helmholtz Munich, Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.
Institute for Diabetes and Obesity, Helmholtz Munich, Neuherberg, Germany.
J Transl Med. 2025 Jan 4;23(1):7. doi: 10.1186/s12967-024-06039-0.
Obese subjects undergoing weight loss often fear the Yoyo dieting effect, which involves regaining or even surpassing their initial weight. To date, our understanding of such long-term obesity and weight cycling effects is still limited and often based on only short-term murine weight gain and loss studies. This study aimed to investigate the long-term impacts of weight cycling on glycemic control and metabolic health, focusing on adipose tissue, liver, and hypothalamus.
Chow-fed mice and mice subjected to prolonged high-fat diet (HFD) consumption for 20 weeks, followed by 24 weeks of dietary interventions to either induce weight gain, weight loss, or weight cycling were monitored for perturbations in feeding efficiency and glucose homeostasis. Post-mortem analyses included qPCR, Western Blotting, biochemical and microscopical assessments for hepatic steatosis and insulin resistance, hypothalamic and adipose tissue inflammation, and circulating lipid, leptin and IL-6 levels.
Weight cycling led to hyperphagia and rapid weight regain, matching the weights of mice continuously on HFD. Despite weight loss, adipose tissue inflammation persisted with elevated pro-inflammatory markers, macrophage infiltration, and impaired Glut4 expression. HFD-induced dysregulation in hypothalamic expression of orexigenic peptides and synaptic plasticity markers persisted also after weight normalization suggesting long-lasting neural alterations. Weight-cycled mice exhibited higher circulating IL-6 and leptin levels, increased hepatic lipid storage, and dysregulated glucose metabolism compared to those with consistent diets, indicating worsened metabolic effects by Yoyo dieting.
In sum, our study highlights significant metabolic risks associated with weight cycling, particularly following prolonged obesity. Persistent adipose tissue inflammation, perturbed neural peptide and plasticity markers and impaired glucose tolerance emphasize the need for effective and sustainable weight loss strategies to mitigate the adverse outcomes of weight regain and improve long-term metabolic health.
正在减肥的肥胖受试者常常担心体重反弹效应,即体重恢复甚至超过其初始体重。迄今为止,我们对这种长期肥胖和体重循环效应的理解仍然有限,且往往仅基于短期小鼠体重增减研究。本研究旨在调查体重循环对血糖控制和代谢健康的长期影响,重点关注脂肪组织、肝脏和下丘脑。
对喂食普通饲料的小鼠以及持续20周食用高脂饮食(HFD),随后进行24周饮食干预以诱导体重增加、体重减轻或体重循环的小鼠,监测其进食效率和葡萄糖稳态的扰动情况。死后分析包括qPCR、蛋白质免疫印迹、对肝脂肪变性和胰岛素抵抗、下丘脑和脂肪组织炎症以及循环脂质、瘦素和白细胞介素-6水平的生化和显微镜评估。
体重循环导致食欲亢进和体重快速恢复,与持续食用HFD的小鼠体重相当。尽管体重减轻,但脂肪组织炎症持续存在,促炎标志物升高、巨噬细胞浸润以及葡萄糖转运蛋白4(Glut4)表达受损。即使体重恢复正常,HFD诱导的下丘脑促食欲肽表达失调和突触可塑性标志物失调仍持续存在,表明存在长期的神经改变。与饮食一致的小鼠相比,体重循环的小鼠循环白细胞介素-6和瘦素水平更高,肝脏脂质储存增加,葡萄糖代谢失调,表明体重反弹节食会使代谢效应恶化。
总之,我们的研究突出了与体重循环相关的重大代谢风险,尤其是在长期肥胖之后。持续的脂肪组织炎症、神经肽和可塑性标志物紊乱以及葡萄糖耐量受损强调了需要有效的可持续减肥策略,以减轻体重恢复的不良后果并改善长期代谢健康。