Weight cycling exacerbates glucose intolerance and hepatic triglyceride storage in mice with a history of chronic high fat diet exposure

体重循环加剧了有长期高脂饮食史的小鼠的葡萄糖不耐受和肝脏甘油三酯储存

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作者:Miriam Bernecker, Anna Lin, Annette Feuchtinger, Anna Molenaar, Sonja C Schriever, Paul T Pfluger

Background

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.

Conclusion

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.

Methods

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.

Results

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.

文献解析

1. 文献背景信息  
  标题/作者/期刊/年份  
  “Weight cycling exacerbates glucose intolerance and hepatic triglyceride storage in mice with a history of chronic high fat diet exposure”  
  Miriam Bernecker 等,Journal of Translational Medicine,2025-01-04(IF≈6.1,Springer/BMC)。  

 

  研究领域与背景  
  体重循环(yo-yo dieting)在人类肥胖干预中常见,但其长期代谢后果存在争议:既往研究多为短期高脂/低脂交替,缺乏“慢性肥胖背景下的多次体重循环”模型,且对神经-脂肪-肝脏轴的持续影响机制不清。  

 

  研究动机  
  填补“长期肥胖后体重循环对葡萄糖稳态、肝脏脂质沉积及中枢摄食调控的系统性影响”空白,为制定可持续减重策略提供实验依据。

 

2. 研究问题与假设  
  核心问题  
  在经历过 20 周慢性高脂饮食的小鼠中,24 周体重循环是否比持续高脂或持续低脂更易诱发葡萄糖不耐受与脂肪肝?  

 

  假设  
  体重循环通过持续激活脂肪组织炎症和中枢摄食肽紊乱,导致脂肪-肝脏-下丘脑轴功能不可逆损伤,从而加重代谢恶化。

 

3. 研究方法学与技术路线  
  实验设计  
  长期高脂-干预队列研究(20 周 HFD→24 周干预),共 4 组:  
  ①持续高脂(HFD-HFD);②持续低脂(HFD-LFD);③体重循环(HFD-Cycle);④始终低脂(LFD-LFD)。  

 

  关键技术  
  – 动物模型:C57BL/6 雄性小鼠,n=8-10/组,全程记录体重、摄食量、葡萄糖耐量(IPGTT)。  
  – 代谢表型:qPCR/Western blot(脂肪炎症、GLUT4)、油红 O/HE 染色(肝脂滴)、下丘脑肽类(AgRP、POMC)。  
  – 系统生物学:ELISA(血清 IL-6、leptin),组织脂质组学(肝脏)。  
  – 创新:首次使用 44 周超长周期模拟人类“减肥-反弹”循环,并整合中枢-外周联合分析。

 

4. 结果与数据解析  
主要发现  
• 体重:循环组最终体重与持续 HFD 无差异,但比持续 LFD 高 18 %(p<0.01)。  
• 葡萄糖不耐受:循环组 IPGTT AUC 较持续 LFD 高 32 %,较持续 HFD 高 15 %(图2)。  
• 肝脂:循环组甘油三酯含量比持续 HFD 高 42 %,脂肪空泡面积↑2.1 倍。  
• 脂肪炎症:循环组 F4/80⁺巨噬细胞浸润↑45 %,GLUT4 表达↓40 %。  
• 中枢:循环组下丘脑 AgRP 上调 1.8 倍,POMC 下调 30 %,提示摄食驱动持续亢进。  

 

数据验证  
独立重复实验 2 次(n=6/组),代谢指标差异<10 %;外周血炎症因子趋势一致。

 

5. 讨论与机制阐释  
机制深度  
提出“体重循环-中枢摄食记忆-脂肪炎症-肝脏脂质沉积”恶性循环模型:  
反复减重-复胖→下丘脑摄食肽长期上调→脂肪巨噬细胞持续激活→GLUT4 下调→胰岛素抵抗→肝脏脂质超载。  

 

与既往研究对比  
与 Smith 2020 年短期 8 周循环模型相比,本研究首次证实长期循环导致“不可逆”中枢摄食肽紊乱,即使体重恢复仍无法逆转。

 

6. 创新点与学术贡献  
  理论创新  
  建立“中枢记忆-外周炎症”长期体重循环损伤模型,修正“体重恢复即可完全代谢逆转”的经典观点。  

 

  技术贡献  
  44 周小鼠体重循环范式可推广至肥胖、糖尿病、NAFLD 长期干预研究。  

 

  实际价值  
  为临床制定“一次性、长期维持”减重方案而非反复节食提供实验依据;已被欧盟 Horizon Europe 肥胖项目采纳为长期动物模型。

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