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一种基于衰老和高脂饮食的新型少肌性肥胖大鼠模型。

A novel rat model of sarcopenic obesity based on aging and high-fat diet consumption.

作者信息

Zhu Huan, Sun Qianqian, Tang Huiyu, Chen Yanyu, Tan Ke, Xu Xu, Wang Shuang

机构信息

The Center of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, 610041, China.

Department of Radiology, West China Hospital of Sichuan University, Chengdu, 610041, China.

出版信息

Biogerontology. 2023 Apr;24(2):235-244. doi: 10.1007/s10522-022-10010-1. Epub 2023 Jan 6.

Abstract

Sarcopenic obesity (SO) is defined as a combination of obesity and sarcopenia, leading to serious health consequences. However, a lack of suitable animal models has hampered research into this disorder. 12-month-old Sprague-Dawley rats were given a high fat content (HFD, SO group) or standard diet (DC groups) for 28 weeks (until 20 months of age). In addition, 2-month-old rats were fed a standard diet as an age control (YC group) until they reached 10 months of age. At the end of the intervention, quadriceps development in the rats was monitored using magnetic resonance examinations and MR spectroscopy. Age-related changes in muscle mass and strength, histopathology, HFD-induced adiposity, and metabolic disturbances were compared between the three groups. Comparing with DC group, rats of SO (20 months, and fed by high-fat diet) exhibited a more prominent loss of muscle mass and strength, a more pronounced decline in myofibre number, IFM, increase in myocyte apoptosis accompanied with increased visceral fat, remarkable glycolipid metabolic disorders, and insulin resistance. However, DC group rats (20 months with standard diet) only showed a decline in quadriceps cross-sectional area/body weight, forelimb grip strength, myofibre cross-sectional area and number, and intermyofibrillar mitochondria number (IFM), increased myocyte apoptosis, without significant metabolic disorder compared with YC group rats. After verifying, SO animal model was successfully set up by HFD induced obesity concomitant with aging-related sarcopenia.

摘要

肌少症肥胖(SO)被定义为肥胖与肌少症的结合,会导致严重的健康后果。然而,缺乏合适的动物模型阻碍了对这种疾病的研究。给12月龄的斯普拉格-道利大鼠喂食高脂肪含量的食物(高脂饮食,SO组)或标准饮食(DC组),持续28周(直至20月龄)。此外,将2月龄大鼠作为年龄对照喂食标准饮食(YC组),直至它们达到10月龄。在干预结束时,使用磁共振检查和磁共振波谱监测大鼠股四头肌的发育情况。比较三组之间肌肉质量和力量、组织病理学、高脂饮食诱导的肥胖以及代谢紊乱的年龄相关变化。与DC组相比,SO组(20月龄,喂食高脂饮食)大鼠表现出更明显的肌肉质量和力量损失、肌纤维数量更显著下降、肌内线粒体(IFM)减少、心肌细胞凋亡增加,同时伴有内脏脂肪增加、明显的糖脂代谢紊乱和胰岛素抵抗。然而,DC组大鼠(20月龄,喂食标准饮食)仅表现出股四头肌横截面积/体重、前肢握力、肌纤维横截面积和数量以及肌原纤维间线粒体数量(IFM)下降,心肌细胞凋亡增加,与YC组大鼠相比无明显代谢紊乱。经证实,通过高脂饮食诱导肥胖并伴有与衰老相关的肌少症成功建立了SO动物模型。

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