Incremental load training improves renal fibrosis by regulating the TGF‑β1/TAK1/MKK3/p38MAPK signaling pathway and inducing the activation of autophagy in aged mice

自噬 纤维化 转化生长因子 激酶 信号转导 癌基因 内科学 分子医学 生物 MAPK/ERK通路 内分泌学 p38丝裂原活化蛋白激酶 细胞凋亡 医学 细胞生物学 细胞周期 生物化学
作者
Chuncha Bao,Zhong Yang,Qiyan Cai,Qian Li,Hongli Li,Bin Shu
出处
期刊:International Journal of Molecular Medicine [Spandidos Publications]
被引量:15
标识
DOI:10.3892/ijmm.2019.4344
摘要

Recent studies have confirmed that kidney tissue fibrosis is closely linked to the natural aging of organs. One of its major characteristics is the reduction of autophagic activity. However, to date, few studies have assessed whether incremental load training is able to improve the occurrence of renal fibrosis caused by natural aging and the underlying mechanisms. In the present study involving male C57/BL mice, an elderly exercise group (OY group) was subjected to progressive load‑increasing rotary‑bar training (5 days/week, lasting for 6 weeks), with an elderly control group (OC group) and a young control group (YC group) used as controls. Renal fibrosis and autophagy‑associated indicators were assessed by Masson's staining, reverse transcription‑quantitative PCR analysis, western blotting, immunofluorescence and transmission electron microscopy. The results suggested that collagen deposition in the basal part of the renal tubular epithelium and glomeruli in the OY group was significantly lower than that in the OC group. In the OC group, the protein expression levels of E‑cadherin, Beclin 1 and light chain 3 were significantly decreased, and increases in α‑smooth muscle actin‑positive signals were observed in the glomerular matrix and renal capsule wall. Furthermore, the expression of transforming growth factor (TGF)‑β1 and its downstream signaling molecules TGF‑β‑activated kinase 1 (TAK1), mitogen‑activated protein kinase (MAPK) kinase (MKK3) and p38MAPK were downregulated following training. The present study confirmed that incremental load training may improve renal fibrosis in aged mice by regulating the TGF‑β1/TAK1/MMK3/p38MAPK signaling pathway and inducing the activation of autophagy to reduce the synthesis of extracellular matrix and delay the epithelial‑mesenchymal transition. The present study provides a novel experimental basis for the intervention of incremental load training to prevent senile renal fibrosis.
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
大幅提高文件上传限制,最高150M (2024-4-1)

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
1秒前
晚晚完成签到 ,获得积分10
1秒前
DD完成签到,获得积分10
2秒前
紫金之巅完成签到 ,获得积分10
2秒前
Bismarck发布了新的文献求助10
2秒前
2秒前
Ava应助努力看文献的小杨采纳,获得10
2秒前
excellent_shit完成签到,获得积分10
3秒前
失眠的血茗完成签到,获得积分10
3秒前
小刘完成签到,获得积分10
4秒前
4秒前
Alden发布了新的文献求助10
5秒前
ypeng发布了新的文献求助10
6秒前
英姑应助勤劳的小蜜蜂采纳,获得10
6秒前
Orange应助Man采纳,获得30
7秒前
8秒前
太阳风暴剑完成签到,获得积分10
11秒前
x1完成签到,获得积分10
11秒前
深情安青应助Bismarck采纳,获得10
11秒前
kuroiMeow完成签到,获得积分10
12秒前
莹莹完成签到 ,获得积分10
13秒前
33完成签到,获得积分10
15秒前
虚心的惮完成签到 ,获得积分10
17秒前
小吴完成签到 ,获得积分10
18秒前
老迟到的可兰完成签到 ,获得积分10
18秒前
背后的小白菜完成签到,获得积分10
19秒前
mmmmmMM完成签到,获得积分10
20秒前
莫友安完成签到,获得积分10
23秒前
zyf完成签到,获得积分10
25秒前
迪迦奥特曼完成签到,获得积分10
25秒前
大方的火龙果完成签到 ,获得积分10
26秒前
huahua完成签到 ,获得积分10
27秒前
ypeng完成签到,获得积分10
28秒前
卡里的乏味完成签到,获得积分10
31秒前
Orange应助Bismarck采纳,获得10
32秒前
32秒前
张星完成签到,获得积分10
33秒前
35秒前
勤奋的大便完成签到 ,获得积分10
36秒前
高傲的小飞龙完成签到,获得积分10
39秒前
高分求助中
The late Devonian Standard Conodont Zonation 2000
Semiconductor Process Reliability in Practice 1500
歯科矯正学 第7版(或第5版) 1004
Nickel superalloy market size, share, growth, trends, and forecast 2023-2030 1000
Smart but Scattered: The Revolutionary Executive Skills Approach to Helping Kids Reach Their Potential (第二版) 1000
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 700
中国区域地质志-山东志 560
热门求助领域 (近24小时)
化学 医学 生物 材料科学 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 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3242069
求助须知:如何正确求助?哪些是违规求助? 2886396
关于积分的说明 8243205
捐赠科研通 2555019
什么是DOI,文献DOI怎么找? 1383201
科研通“疑难数据库(出版商)”最低求助积分说明 649672
邀请新用户注册赠送积分活动 625417