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食物限制对高脂饮食诱导的肥胖心脏的抗凋亡和促存活作用。

Anti-apoptotic and Pro-survival Effects of Food Restriction on High-Fat Diet-Induced Obese Hearts.

作者信息

Lin Yi-Yuan, Hsieh Po-Shiuan, Cheng Yu-Jung, Cheng Shiu-Min, Chen Chiao-Nan Joyce, Huang Chih-Yang, Kuo Chia-Hua, Kao Chung-Lan, Shyu Woei-Cherng, Lee Shin-Da

机构信息

Graduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.

Department of Physiology and Biophysics, National Defense Medical Center, Taipei, Taiwan.

出版信息

Cardiovasc Toxicol. 2017 Apr;17(2):163-174. doi: 10.1007/s12012-016-9370-2.

Abstract

Food restriction and weight loss are known to prevent obesity-related heart diseases. This study investigates whether food restriction elicits anti-apoptotic and pro-survival effects on high-fat diet-induced obese hearts. Histopathological analysis, TUNEL assay, and Western blotting were performed on the excised hearts from three groups of Sprague-Dawley rats which were fed with regular chow diet (CON, 13.5 % fat), a high-fat ad libitum diet (HFa, 45 % fat), or a high-fat food-restricted diet (HFr, 45 % fat, maintaining the same weight as CON) for 12 weeks. Body weight, blood pressure, heart weight, triglycerides, insulin, HOMA, interstitial spaces, cardiac fibrosis, and cardiac TUNEL-positive apoptotic cells were increased in HFa relative to CON, whereas these parameters were decreased in HFr relative to HFa. The protein levels of cardiac Fas ligand, Fas receptors, Fas-associated death domain (FADD), activated caspase-8, and activated caspase-3 (Fas receptor-dependent apoptotic pathways), as well as t-Bid/Bid, Bax/Bcl-2, Bad/p-Bad, Cytochrome c, activated caspase-9, and activated caspase-3 (mitochondria-dependent apoptotic pathways) in HFr were lower than those in HFa. Moreover, the Bcl-xL and IGF-1-related components of IGF-1, p-PI3 K/PI3 K, p-Akt/Akt in HFr were higher than those in HFa. Our findings suggest that a restricted high-fat diet for maintaining weight control could diminish cardiac Fas receptor-dependent and mitochondria-dependent apoptotic pathways as well as might enhance IGF-1-related pro-survival pathways. In sum, food restriction for maintaining normal weight could elicit anti-apoptotic and pro-survival effects on high-fat diet-induced obese hearts.

摘要

已知食物限制和体重减轻可预防肥胖相关的心脏病。本研究调查食物限制是否对高脂饮食诱导的肥胖心脏产生抗凋亡和促生存作用。对三组Sprague-Dawley大鼠的离体心脏进行组织病理学分析、TUNEL检测和蛋白质印迹分析,这三组大鼠分别喂食常规饲料(CON,脂肪含量13.5%)、高脂自由采食饮食(HFa,脂肪含量45%)或高脂食物限制饮食(HFr,脂肪含量45%,体重维持与CON相同)12周。与CON组相比,HFa组的体重、血压、心脏重量、甘油三酯、胰岛素、HOMA、间质间隙、心脏纤维化和心脏TUNEL阳性凋亡细胞增加,而与HFa组相比,HFr组的这些参数降低。HFr组心脏Fas配体、Fas受体、Fas相关死亡结构域(FADD)、活化的caspase-8和活化的caspase-3(Fas受体依赖性凋亡途径)以及t-Bid/Bid、Bax/Bcl-2、Bad/p-Bad、细胞色素c、活化的caspase-9和活化的caspase-3(线粒体依赖性凋亡途径)的蛋白质水平低于HFa组。此外,HFr组中IGF-1的Bcl-xL和IGF-1相关成分、p-PI3 K/PI3 K、p-Akt/Akt高于HFa组。我们的研究结果表明,限制高脂饮食以维持体重控制可减少心脏Fas受体依赖性和线粒体依赖性凋亡途径,并且可能增强IGF-1相关的促生存途径。总之,限制食物摄入以维持正常体重可对高脂饮食诱导的肥胖心脏产生抗凋亡和促生存作用。

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