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

内分泌学 内科学 表达式(计算机科学) 医学 生理学 计算机科学 程序设计语言
作者
Ana P. Pinto,Vitor Rosetto Muñoz,Maria Eduarda Almeida Tavares,Jonathas Rodrigo dos Santos,Macário Arosti Rebelo,Luciane C. Alberici,Fernando Moreira Simabuco,Giovana Rampazzo Teixeira,José Rodrigo Pauli,Leandro Pereira de Moura,Dennys E. Cintra,Eduardo R. Ropelle,Ellen Cristini de Freitas,Donato A. Rivas,Adelino Sánchez Ramos da Silva
出处
期刊:Life Sciences [Elsevier BV]
卷期号:312: 121175-121175 被引量:5
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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
咕噜咕噜完成签到,获得积分20
3秒前
辛勤雨泽发布了新的文献求助10
3秒前
3秒前
Ava应助科研通管家采纳,获得10
4秒前
wanci应助科研通管家采纳,获得10
5秒前
坦率的匪应助科研通管家采纳,获得10
5秒前
所所应助科研通管家采纳,获得10
5秒前
坦率的匪应助科研通管家采纳,获得10
5秒前
Hello应助科研通管家采纳,获得10
5秒前
今后应助科研通管家采纳,获得10
5秒前
5秒前
5秒前
5秒前
李爱国应助科研通管家采纳,获得10
5秒前
5秒前
大个应助科研通管家采纳,获得10
5秒前
在水一方应助科研通管家采纳,获得10
5秒前
F妮妮完成签到,获得积分10
5秒前
Rondab应助典雅的飞丹采纳,获得50
10秒前
生动路人应助飞云采纳,获得10
13秒前
深情安青应助Scinature采纳,获得10
14秒前
科研通AI5应助雷培采纳,获得10
14秒前
爆米花应助实心小墩墩采纳,获得10
16秒前
17秒前
hh发布了新的文献求助10
17秒前
123456完成签到,获得积分10
19秒前
咕噜咕噜发布了新的文献求助10
19秒前
欧气青年发布了新的文献求助10
21秒前
zhenzheng完成签到 ,获得积分10
22秒前
漂泊发布了新的文献求助10
22秒前
等待冰露发布了新的文献求助10
22秒前
华仔应助薄冰采纳,获得10
22秒前
高高诗柳完成签到 ,获得积分10
25秒前
比亚迪士尼在逃公主完成签到,获得积分10
26秒前
隐形道之完成签到,获得积分10
26秒前
hh完成签到,获得积分10
27秒前
小林神完成签到,获得积分10
27秒前
28秒前
28秒前
高分求助中
The Mother of All Tableaux: Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 3000
A new approach to the extrapolation of accelerated life test data 1000
Problems of point-blast theory 400
Indomethacinのヒトにおける経皮吸収 400
北师大毕业论文 基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 390
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
Robot-supported joining of reinforcement textiles with one-sided sewing heads 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3997679
求助须知:如何正确求助?哪些是违规求助? 3537190
关于积分的说明 11270985
捐赠科研通 3276344
什么是DOI,文献DOI怎么找? 1806900
邀请新用户注册赠送积分活动 883582
科研通“疑难数据库(出版商)”最低求助积分说明 809975