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联合体育锻炼可逆转老年小鼠肝脏中 Bmal1 的表达减少。

Combined physical exercise reverses the reduced expression of Bmal1 in the liver of aged mice.

机构信息

School of Physical Education and Sport of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil.

Multicentric Program of Postgraduate in Physiological Sciences, São Paulo State University (UNESP), School of Dentistry of Araçatuba, Araçatuba, São Paulo, Brazil.

出版信息

Life Sci. 2023 Jan 1;312:121175. doi: 10.1016/j.lfs.2022.121175. Epub 2022 Nov 19.

Abstract

Aging can modify the morphology and function of the liver, such as generating a decrease in the mitochondria content, autophagy, and cell senescence. Although exercise training has several beneficial effects on hepatic metabolism, its actions on autophagy processes, mitochondrial function, and cellular senescence need to be more widely explored. The present study verified the effects of aging and exercise on hepatic circadian markers, autophagy, and mitochondria activity in 24-month-old mice with a combined exercise training protocol. In addition, we used public datasets from human livers in several conditions and BMAL1 knockout mice. C57BL/6 mice were distributed into Control (CT, young, 6-month-old mice), sedentary old (Old Sed, sedentary, 24-month-old mice), and exercised old (Old Ex, 24-month-old mice submitted to a combined exercise training protocol). The exercise training protocol consisted of three days of endurance exercise - treadmill running, and two days of resistance exercise - climbing a ladder, for three weeks. At the end of the protocol, the liver was removed and prepared for histological analysis, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), immunoblotting technique, and oxygen consumption. Heatmaps were built using a human dataset and Bmal1 knockout samples. In summary, the Old Sed had reduced strength, coordination, and balance, as well as a decrease in Bmal1 expression and the presence of degenerated liver cells. Still, this group upregulated the transcription factors related to mitochondrial biogenesis. The Old Ex group had increased strength, coordination, and balance, improved glucose sensitivity, as well as restored Bmal1 expression and the mitochondrial transcription factors. The human datasets indicated that mitochondrial markers and autophagy strongly correlate with specific liver diseases but not aging. We can speculate that mitochondrial and autophagy molecular markers alterations may depend on long-term training.

摘要

衰老会改变肝脏的形态和功能,例如减少线粒体含量、自噬和细胞衰老。尽管运动训练对肝脏代谢有多种有益作用,但它对自噬过程、线粒体功能和细胞衰老的作用需要更广泛的探索。本研究通过联合运动训练方案验证了衰老和运动对 24 个月大的小鼠肝脏生物钟标记物、自噬和线粒体活性的影响。此外,我们使用了来自人类肝脏多种状态和 BMAL1 敲除小鼠的公共数据集。C57BL/6 小鼠分为对照组(CT,年轻,6 月龄小鼠)、久坐不动的老年组(Old Sed,久坐不动,24 月龄小鼠)和运动的老年组(Old Ex,24 月龄小鼠接受联合运动训练方案)。运动训练方案由三天的耐力运动 - 跑步机跑步和两天的抗阻运动 - 爬梯组成,持续三周。在方案结束时,取出肝脏进行组织学分析、逆转录定量聚合酶链反应(RT-qPCR)、免疫印迹技术和耗氧量测定。使用人类数据集和 Bmal1 敲除样本构建热图。总之,Old Sed 组小鼠的力量、协调性和平衡能力下降,Bmal1 表达降低,肝细胞退化。尽管如此,该组上调了与线粒体生物发生相关的转录因子。Old Ex 组小鼠的力量、协调性和平衡能力提高,葡萄糖敏感性增强,Bmal1 表达和线粒体转录因子得到恢复。人类数据集表明,线粒体标志物和自噬与特定的肝脏疾病强烈相关,但与衰老无关。我们可以推测,线粒体和自噬分子标志物的改变可能取决于长期训练。

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