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力量训练改变了肥胖小鼠组织中脂肪酸的组成,略微改善了脂肪组织中的产热途径。

Strength training alters the tissue fatty acids profile and slightly improves the thermogenic pathway in the adipose tissue of obese mice.

机构信息

Exercise Cellular Biology Laboratory, University of Campinas, Limeira, São Paulo, Brazil.

Laboratory of Molecular Biology of Exercise, School of Applied Sciences, University of Campinas, Limeira, São Paulo, Brazil.

出版信息

Sci Rep. 2022 Apr 28;12(1):6913. doi: 10.1038/s41598-022-10688-w.

Abstract

Obesity is a disease characterized by the exacerbated increase of adipose tissue. A possible way to decrease the harmful effects of excessive adipose tissue is to increase the thermogenesis process, to the greater energy expenditure generated by the increase in heat in the body. In adipose tissue, the thermogenesis process is the result of an increase in mitochondrial work, having as substrate H ions, and which is related to the increased activity of UCP1. Evidence shows that stress is responsible for increasing the greater induction of UCP1 expression via β-adrenergic receptors. It is known that physical exercise is an important implement for sympathetic stimulation promoting communication between norepinephrine/epinephrine with membrane receptors. Thus, the present study investigates the influence of short-term strength training (STST) on fatty acid composition, lipolysis, lipogenesis, and browning processes in the subcutaneous adipose tissue (sWAT) of obese mice. For this, Swiss mice were divided into three groups: lean control, obesity sedentary, and obese strength training (OBexT). Obese animals were fed a high-fat diet for 14 weeks. Trained obese animals were submitted to 7 days of strength exercise. It was demonstrated that STST sessions were able to reduce fasting glycemia. In the sWAT, the STST was able to decrease the levels of the long-chain fatty acids profile, saturated fatty acid, and palmitic fatty acid (C16:0). Moreover, it was showed that STST did not increase protein levels responsible for lipolysis, the ATGL, ABHD5, pPLIN1, and pHSL. On the other hand, the exercise protocol decreased the expression of the lipogenic enzyme SCD1. Finally, our study demonstrated that the STST increased browning process-related genes such as PGC-1α, PRDM16, and UCP1 in the sWAT. Interestingly, all these biomolecular mechanisms have been observed independently of changes in body weight. Therefore, it is concluded that short-term strength exercise can be an effective strategy to initiate morphological changes in sWAT.

摘要

肥胖是一种以脂肪组织过度增加为特征的疾病。减少过多脂肪组织有害影响的一种可能方法是增加产热过程,从而增加身体热量产生的更大能量消耗。在脂肪组织中,产热过程是线粒体工作增加的结果,其底物为 H 离子,这与 UCP1 活性的增加有关。有证据表明,应激通过β-肾上腺素能受体负责增加 UCP1 表达的更大诱导。众所周知,运动是刺激交感神经的重要手段,促进去甲肾上腺素/肾上腺素与膜受体之间的通讯。因此,本研究调查了短期力量训练(STST)对肥胖小鼠皮下脂肪组织(sWAT)中脂肪酸组成、脂肪分解、脂肪生成和褐变过程的影响。为此,将瑞士小鼠分为三组:瘦对照组、肥胖静坐组和肥胖力量训练组(OBexT)。肥胖动物喂食高脂肪饮食 14 周。训练肥胖动物进行了 7 天的力量运动。结果表明,STST 会议能够降低空腹血糖。在 sWAT 中,STST 能够降低长链脂肪酸谱、饱和脂肪酸和棕榈酸(C16:0)的水平。此外,研究表明,STST 并没有增加负责脂肪分解的蛋白水平,如 ATGL、ABHD5、pPLIN1 和 pHSL。另一方面,运动方案降低了脂肪生成酶 SCD1 的表达。最后,我们的研究表明,STST 增加了 sWAT 中与褐变过程相关的基因,如 PGC-1α、PRDM16 和 UCP1 的表达。有趣的是,所有这些生物分子机制都独立于体重变化而观察到。因此,结论是短期力量运动可以成为启动 sWAT 形态变化的有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c1f/9050661/132e363a8396/41598_2022_10688_Fig1_HTML.jpg

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