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

耐力训练 线粒体生物发生 衰老 自噬 内分泌学 内科学 生物 昼夜节律 基因剔除小鼠 线粒体 医学 细胞生物学 生物化学 细胞凋亡 受体
作者
Ana P. Pinto,Vitor Rosetto Muñoz,Maria Eduarda A. Tavares,Jonathas R. dos Santos,Macario A. Rebelo,Luciane Carla Alberici,Fernando Moreira Simabuco,Giovana Rampazzo Teixeira,José Rodrigo Pauli,Leandro Pereira de Moura,Dennys Esper Cintra,Eduardo R. Ropelle,Ellen Cristini de Freitas,Donato A. Rivas,Adelino Sánchez Ramos da Silva
出处
期刊:Life Sciences [Elsevier]
卷期号:312: 121175-121175 被引量:2
标识
DOI:10.1016/j.lfs.2022.121175
摘要

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.
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