High-Intensity Interval Training Improves Cardiac Function by miR-206 Dependent HSP60 Induction in Diabetic Rats

高强度间歇训练 医学 内科学 间歇训练 糖尿病性心肌病 内分泌学 心脏病学 心功能曲线 心肌病 心力衰竭
作者
Maryam Delfan,Raheleh Amadeh Juybari,Sattar Gorgani‐Firuzjaee,Jens Høiriis Nielsen,Neda Delfan,Ismail Laher,Ayoub Saeidi,Urs Granacher,Hassane Zouhal
出处
期刊:Frontiers in Cardiovascular Medicine [Frontiers Media SA]
卷期号:9 被引量:3
标识
DOI:10.3389/fcvm.2022.927956
摘要

A role for microRNAs is implicated in several biological and pathological processes. We investigated the effects of high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) on molecular markers of diabetic cardiomyopathy in rats.Eighteen male Wistar rats (260 ± 10 g; aged 8 weeks) with streptozotocin (STZ)-induced type 1 diabetes mellitus (55 mg/kg, IP) were randomly allocated to three groups: control, MICT, and HIIT. The two different training protocols were performed 5 days each week for 5 weeks. Cardiac performance (end-systolic and end-diastolic dimensions, ejection fraction), the expression of miR-206, HSP60, and markers of apoptosis (cleaved PARP and cytochrome C) were determined at the end of the exercise interventions.Both exercise interventions (HIIT and MICT) decreased blood glucose levels and improved cardiac performance, with greater changes in the HIIT group (p < 0.001, η2: 0.909). While the expressions of miR-206 and apoptotic markers decreased in both training protocols (p < 0.001, η2: 0.967), HIIT caused greater reductions in apoptotic markers and produced a 20% greater reduction in miR-206 compared with the MICT protocol (p < 0.001). Furthermore, both training protocols enhanced the expression of HSP60 (p < 0.001, η2: 0.976), with a nearly 50% greater increase in the HIIT group compared with MICT.Our results indicate that both exercise protocols, HIIT and MICT, have the potential to reduce diabetic cardiomyopathy by modifying the expression of miR-206 and its downstream targets of apoptosis. It seems however that HIIT is even more effective than MICT to modulate these molecular markers.
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
刚刚
蓝胖胖蓝完成签到,获得积分10
刚刚
徐徐发布了新的文献求助10
1秒前
大个应助刻苦的白梅采纳,获得30
1秒前
纳木错的蓝完成签到,获得积分10
1秒前
LINTING完成签到,获得积分10
2秒前
Hello应助科研通管家采纳,获得10
2秒前
Owen应助科研通管家采纳,获得10
2秒前
2秒前
元元应助科研通管家采纳,获得20
2秒前
李爱国应助科研通管家采纳,获得10
2秒前
薄荷小姐完成签到 ,获得积分10
2秒前
CodeCraft应助科研通管家采纳,获得10
2秒前
英姑应助科研通管家采纳,获得10
2秒前
完美世界应助科研通管家采纳,获得10
2秒前
老鼠咕噜应助科研通管家采纳,获得10
2秒前
斯文败类应助科研通管家采纳,获得10
3秒前
学习快乐应助科研通管家采纳,获得50
3秒前
3秒前
dyd完成签到,获得积分10
3秒前
外向青筠关注了科研通微信公众号
4秒前
圣洁发布了新的文献求助10
4秒前
ygd完成签到,获得积分10
4秒前
在路上发布了新的文献求助10
4秒前
5秒前
侯冰珍完成签到,获得积分10
6秒前
7秒前
msd2phd完成签到,获得积分10
7秒前
柚子发布了新的文献求助10
7秒前
7秒前
咪咪完成签到,获得积分10
7秒前
8秒前
谨慎的豆芽完成签到,获得积分10
9秒前
情怀应助飞快的寒香采纳,获得10
9秒前
27完成签到,获得积分10
9秒前
研友_VZG7GZ应助ygd采纳,获得10
9秒前
小白完成签到 ,获得积分10
12秒前
13秒前
阿泽发布了新的文献求助10
13秒前
祖乐松完成签到,获得积分10
13秒前
高分求助中
Thermodynamic data for steelmaking 3000
Teaching Social and Emotional Learning in Physical Education 900
Counseling With Immigrants, Refugees, and Their Families From Social Justice Perspectives pages 800
藍からはじまる蛍光性トリプタンスリン研究 400
Cardiology: Board and Certification Review 400
[Lambert-Eaton syndrome without calcium channel autoantibodies] 340
NEW VALUES OF SOLUBILITY PARAMETERS FROM VAPOR PRESSURE DATA 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 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 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2362477
求助须知:如何正确求助?哪些是违规求助? 2070482
关于积分的说明 5173360
捐赠科研通 1798786
什么是DOI,文献DOI怎么找? 898203
版权声明 557785
科研通“疑难数据库(出版商)”最低求助积分说明 479410