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实验性肥胖对膈肌结构、功能和生物能量学的影响。

Impact of experimental obesity on diaphragm structure, function, and bioenergetics.

机构信息

Laboratory of Pulmonary Investigation, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

Fluminense Federal University, Niteroi, Brazil.

出版信息

J Appl Physiol (1985). 2020 Nov 1;129(5):1062-1074. doi: 10.1152/japplphysiol.00262.2020. Epub 2020 Sep 10.

Abstract

Obesity is associated with bioenergetic dysfunction of peripheral muscles; however, little is known regarding the impact of obesity on the diaphragm. We hypothesized that obesity would be associated with diaphragm dysfunction attributable to mitochondrial oxygen consumption and structural and ultrastructural changes. Wistar rat litters were culled to 3 pups to induce early postnatal overfeeding and consequent obesity. Control animals were obtained from unculled litters. From , diaphragm ultrasound, computed tomography, high-resolution respirometry, immunohistochemical, biomolecular, and ultrastructural histological analyses were performed. The diaphragms of obese animals, compared with those of controls, presented changes in morphology as increased thickening fraction, diaphragm excursion, and diaphragm dome height, as well as increased mitochondrial respiratory capacity coupled to ATP synthesis and maximal respiratory capacity. Fatty acid synthase gene expression was also higher in obese animals, suggesting a source of energy for the respiratory chain. Myosin heavy chain-IIA was increased, indicating shift from glycolytic toward oxidative muscle fiber profile. Diaphragm tissue also exhibited ultrastructural changes, such as compact, round, and swollen mitochondria with fainter cristae and more lysosomal bodies. Dynamin-1 expression in the diaphragm was reduced in obese rats, suggesting decreased mitochondrial fission. Furthermore, gene expressions of peroxisome γ proliferator-activated receptor coactivator-1α and superoxide dismutase-2 were lower in obese animals than in controls, which may indicate a predisposition to oxidative injury. In conclusion, in the obesity model used herein, muscle fiber phenotype was altered in a manner likely associated with increased mitochondrial respiratory capability, suggesting respiratory adaptation to increased metabolic demand. Obesity has been associated with peripheral muscle dysfunction; however, little is known about its impact on the diaphragm. In the current study, we found high oxygen consumption in diaphragm tissue and changes in muscle fiber phenotypes toward a more oxidative profile in experimental obesity.

摘要

肥胖与周围肌肉的生物能量功能障碍有关;然而,对于肥胖对膈肌的影响知之甚少。我们假设肥胖与膈肌功能障碍有关,这归因于线粒体耗氧量以及结构和超微结构的变化。Wistar 大鼠幼仔被剔除至 3 只,以诱导早期产后过度喂养和随后的肥胖。对照动物来自未剔除的幼仔。从出生后第 7 天到第 21 天,进行了膈肌超声、计算机断层扫描、高分辨率呼吸测量、免疫组织化学、生物分子和超微结构组织学分析。与对照组相比,肥胖动物的膈肌形态发生了变化,表现为增厚分数、膈肌位移和膈肌穹顶高度增加,以及与 ATP 合成和最大呼吸能力偶联的线粒体呼吸能力增加。脂肪酸合酶基因的表达也在肥胖动物中增加,表明这是呼吸链的能量来源。肌球蛋白重链-IIA 增加,表明从糖酵解向氧化肌纤维谱的转变。膈肌组织还表现出超微结构变化,如致密、圆形和肿胀的线粒体,嵴较淡,溶酶体体较多。肥胖大鼠膈肌中的动力蛋白-1 表达减少,表明线粒体裂变减少。此外,肥胖动物的过氧化物酶体 γ 增殖物激活受体共激活因子-1α 和超氧化物歧化酶-2 的基因表达低于对照组,这可能表明易发生氧化损伤。总之,在本文使用的肥胖模型中,肌肉纤维表型发生改变,可能与线粒体呼吸能力增加有关,表明呼吸适应增加的代谢需求。肥胖与周围肌肉功能障碍有关;然而,对于其对膈肌的影响知之甚少。在本研究中,我们发现实验性肥胖中膈肌组织的耗氧量较高,并且肌肉纤维表型向更氧化的表型发生变化。

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