Literature DB >> 28550760

Exercise training ameliorates matrix metalloproteinases 2 and 9 messenger RNA expression and mitigates adverse left ventricular remodeling in streptozotocin-induced diabetic rats.

Flávio S Silva1, Raul H Bortolin2, Diego N Araújo3, Dáfiny E S Marques4, João Paulo M S Lima5, Adriana A Rezende2, Wouber H B Vieira6, Naisandra B Silva4, Karina C P Medeiros4, Paul W Ackermann7, Bento J Abreu4, Fernando A L Dias3.   

Abstract

BACKGROUND: The aim was to investigate whether exercise training (ExT) would ameliorate expression of key genes for myocardial morphostructure and mitigate adverse left ventricular (LV) remodeling in experimental type 1 diabetes (T1D). METHODS AND
RESULTS: Male Wistar rats were divided into four groups: sedentary control (SC, n=9), trained control (TC, n=13), sedentary diabetic (SD, n=20), and trained diabetic (TD, n=17). T1D was induced by 40 mg/kg streptozotocin (single dose, i.v.). Training program consisted of 4-week treadmill running (60 min/day, 5 days/wk). Structure of the LV was evaluated using histomorphometric techniques. Gene expression changes of LV collagens I and III, metalloproteinases (MMPs) 2 and 9, and transforming growth factor-β1 were detected by reverse transcriptase quantitative polymerase chain reaction. Compared with SC, SD rats presented LV eccentric remodeling, myocyte hypertrophy, and fibrosis, whereas TD animals showed normal LV geometry and collagen content but thinner myocytes. Expression of collagens and type I/III collagen messenger RNA (mRNA) ratio were diminished in diabetic hearts compared with SC. MMP-2 gene was down-regulated in SD, whereas TD group showed decreased MMP-9 mRNA levels and MMP-2 expression comparable to that of SC rats.
CONCLUSIONS: Attenuation of MMP-2 down-regulation and reduction in MMP-9 mRNA expression may constitute an underlying mechanism by which ExT counteracts progression of adverse LV remodeling in T1D.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Exercise; Extracellular matrix; Heart; Rats; Type 1 diabetes

Mesh:

Substances:

Year:  2017        PMID: 28550760     DOI: 10.1016/j.carpath.2017.05.003

Source DB:  PubMed          Journal:  Cardiovasc Pathol        ISSN: 1054-8807            Impact factor:   2.185


  4 in total

1.  Effect of Irbesartan on AGEs-RAGE and MMPs systems in rat type 2 diabetes myocardial-fibrosis model.

Authors:  Ye Hongwei; Cao Ruiping; Fang Yingyan; Zhang Guanjun; Hu Jie; Liu Xingyu; Tang Jie; Li Zhenghong; Gao Qin; Hu Junfeng; Zhang Heng
Journal:  Exp Biol Med (Maywood)       Date:  2019-04-26

2.  Long-term moderate intensity exercise alleviates myocardial fibrosis in type 2 diabetic rats via inhibitions of oxidative stress and TGF-β1/Smad pathway.

Authors:  Shi-Qiang Wang; Dan Li; Yang Yuan
Journal:  J Physiol Sci       Date:  2019-08-07       Impact factor: 2.781

3.  Role of Artesunate on cardiovascular complications in rats with type 1 diabetes mellitus.

Authors:  Yi Chen; Wei Li; Xiaolin Nong; Chen Liang; Jiaquan Li; Wei Lu; Bingge Wang; Zhong Yuan; Shiying Yang
Journal:  BMC Endocr Disord       Date:  2021-01-26       Impact factor: 2.763

4.  FTZ Ameliorates Diabetic Cardiomyopathy by Inhibiting Inflammation and Cardiac Fibrosis in the Streptozotocin-Induced Model.

Authors:  Lexun Wang; Huijuan Wu; Yanyue Deng; Shengxi Zhang; Quxing Wei; Qianqian Yang; Shenghua Piao; Weijian Bei; Xianglu Rong; Jiao Guo
Journal:  Evid Based Complement Alternat Med       Date:  2021-09-28       Impact factor: 2.629

  4 in total

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