高心肺适能在肥胖引起的早衰中对代谢、心脏和大脑的分子损伤有更高的保护作用。

Endocrinology and metabolism (Seoul, Korea) Pub Date : 2022-08-01 Epub Date: 2022-08-05 DOI:10.3803/EnM.2022.1430
Patcharapong Pantiya, Chanisa Thonusin, Natticha Sumneang, Benjamin Ongnok, Titikorn Chunchai, Sasiwan Kerdphoo, Thidarat Jaiwongkam, Busarin Arunsak, Natthaphat Siri-Angkul, Sirawit Sriwichaiin, Nipon Chattipakorn, Siriporn C Chattipakorn
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引用次数: 2

摘要

背景:高心肺适能(CRF)可以预防与年龄相关的疾病。然而,在非肥胖和肥胖的情况下,高内在CRF对代谢、心脏和脑损伤的保护作用的机制仍然不完全清楚。我们的目的是确定高内在CRF在非肥胖大鼠和肥胖未训练大鼠中防止代谢、心脏和脑损伤的机制。方法:将7周龄雄性Wistar大鼠分为两组(每组8只),给予正常饮食和高脂饮食(HFD)。在第12周和第28周,评估CRF、碳水化合物和脂肪酸氧化、心功能和代谢参数。第28周进行行为测试。在第28周结束时,对大鼠实施安乐死,以收集心脏和大脑样本用于分子研究。结果:肥胖大鼠的衰老相关参数值高于非肥胖大鼠,表明肥胖大鼠经历了肥胖诱导的早衰。在随访中,高基线CRF水平与一些有利的代谢、心脏和脑参数呈正相关。具体来说,高CRF对代谢、心脏和脑损伤的保护作用是通过调节体重和组成、脂质谱、底物氧化、线粒体功能、胰岛素信号、自噬、细胞凋亡、炎症、氧化应激、心功能、神经发生、血脑屏障、突触功能、阿尔茨海默病相关蛋白的积累和认知来介导的。有趣的是,这种效果在喂食hfd的大鼠中更为明显。结论:高CRF的保护作用是通过多种机制调节的。这些影响在肥胖引起的早衰条件下表现出更大的功效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High Cardiorespiratory Fitness Protects against Molecular Impairments of Metabolism, Heart, and Brain with Higher Efficacy in Obesity-Induced Premature Aging.

Backgruound: High cardiorespiratory fitness (CRF) protects against age-related diseases. However, the mechanisms mediating the protective effect of high intrinsic CRF against metabolic, cardiac, and brain impairments in non-obese versus obese conditions remain incompletely understood. We aimed to identify the mechanisms through which high intrinsic CRF protects against metabolic, cardiac, and brain impairments in non-obese versus obese untrained rats.

Methods: Seven-week-old male Wistar rats were divided into two groups (n=8 per group) to receive either a normal diet or a highfat diet (HFD). At weeks 12 and 28, CRF, carbohydrate and fatty acid oxidation, cardiac function, and metabolic parameters were evaluated. At week 28, behavior tests were performed. At the end of week 28, rats were euthanized to collect heart and brain samples for molecular studies.

Results: The obese rats exhibited higher values for aging-related parameters than the non-obese rats, indicating that they experienced obesity-induced premature aging. High baseline CRF levels were positively correlated with several favorable metabolic, cardiac, and brain parameters at follow-up. Specifically, the protective effects of high CRF against metabolic, cardiac, and brain impairments were mediated by the modulation of body weight and composition, the lipid profile, substrate oxidation, mitochondrial function, insulin signaling, autophagy, apoptosis, inflammation, oxidative stress, cardiac function, neurogenesis, blood-brain barrier, synaptic function, accumulation of Alzheimer's disease-related proteins, and cognition. Interestingly, this effect was more obvious in HFD-fed rats.

Conclusion: The protective effect of high CRF is mediated by the modulation of several mechanisms. These effects exhibit greater efficacy under conditions of obesity-induced premature aging.

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