Alterations of relaxin and its receptor system components in experimental diabetic cardiomyopathy rats
Alterations of relaxin and its receptor system components in experimental diabetic cardiomyopathy rats
复制标题
实验性糖尿病心肌病大鼠松弛素及其受体系统成分的变化
DOI:
10.1007/s00441-017-2662-4
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发表时间:
2017-08
影响因子:
3.6
通讯作者:
Yin Xinhua
中科院分区:
文献类型:
--
作者:
Zhang Xiaohui;Pan Liya;Yang Kelaier;Fu Yu;Liu Yue;Chen Wenjia;Ma Xiao;Yin Xinhua
High glucose induces apoptosis of cardiomyocytes and fibrosis of cardiac fibroblasts, contributing to diabetic cardiomyopathy. In this work, we explore the production of relaxin alterations and the significance of their receptor system components in the hearts of experimental diabetic cardiomyopathy rats. We measured rat relaxin-1 (equivalent to human relaxin-2), relaxin-3, RXFP1 and RXFP3 mRNA expression in the hearts of experimental diabetic cardiomyopathy rats. Neonatal rat ventricular myocytes (NRVMs) and cardiac fibroblasts were treated with 5.5 mmol/l normal glucose (NG) and 33 mmol/l high glucose (HG) for 0, 6, 12, 24, 48 and 72 h. Ratrelaxin-1, relaxin-3, RXFP1 and RXFP3mRNA expression were determined by real-time PCR. In the present study, we offer the first evidence thatRelaxin-1mRNA significantly increased andRelaxin-3mRNA expression decreased at 4 and 8 weeks after STZ in the hearts of diabetic rats. In addition, significant down regulation of the mRNA expression ofRXFP1andRXFP3was observed at 4 w after STZ; however, the mRNA expression levels ofRXFP1andRXFP3were increased at 8 weeks after STZ. Apoptotic NRVMs induced by high glucose generate a decreased level ofrelaxin-1andRXFP1. In HG-administered cardiac fibroblasts,Relaxin-1mRNA was significantly increased andrelaxin-3mRNA was significantly decreased. Additionally, the mRNA expression ofRXFP1was decreased, and the mRNA expression ofRXFP3was increased. This results showed that an important role of relaxin-2, relaxin-3 and their receptors system in the regulation of diabetic cardiomyopathy.
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影响因子:
1.6
作者:
Linda J. Chan;M. Hossain;C. Samuel;F. Separovic;J. Wade
通讯作者:
Linda J. Chan;M. Hossain;C. Samuel;F. Separovic;J. Wade
影响因子:
2.9
作者:
Hossain, Mohammed Akhter;Man, Bryna Chow Suet;Samuel, Chrishan S.
通讯作者:
Samuel, Chrishan S.
影响因子:
3
作者:
Otsubo, Hiroki;Onaka, Tatsushi;Ueta, Yoichi
通讯作者:
Ueta, Yoichi
影响因子:
5.7
作者:
Voors, Adriaan A.;van der Horst, Iwan C. C.
通讯作者:
van der Horst, Iwan C. C.
影响因子:
168.9
作者:
Teerlink, John R.;Metra, Marco;Cotter, Gad
通讯作者:
Cotter, Gad