Literature DB >> 26821570

Chronic Administration of Catestatin Improves Autonomic Function and Exerts Cardioprotective Effects in Myocardial Infarction Rats.

Dandan Wang1, Tao Liu1, Shaobo Shi1, Ran Li1, Yingguang Shan1, Yan Huang1, Dan Hu2, Congxin Huang3.   

Abstract

Catestatin (CST), which is emerging as a novel cardiac modulator, can protect the heart against excessive sympathetic drive in hypertensive cardiomyopathy. The aim of this study is to investigate whether exogenous CST decreases excessive cardiac sympathetic drive and improves autonomic function and exerts cardioprotective effects in myocardial infarction (MI) rats. Rats were divided into a sham group, MI group, and MI plus CST (MI + CST) group. Four weeks later, the autonomic function of the animals was assessed by analyzing heart rate variability (HRV) and measuring plasma catecholamine. Cardiac function was evaluated via echocardiography. Electrophysiological characteristics were assessed in Langendorff-perfused hearts. Compared to the MI group, the chronic administration of CST significantly increased the standard deviation of normal-normal intervals (P < .01) and low-frequency (LF) and high-frequency (HF) HRV and decreased the ratio of LF-HF HRV (P < .01 for all). Additionally, the level of plasma catecholamine was reduced in the MI + CST group compared to the MI group (P < .01). Treatment with CST significantly increased ejection fraction (EF) and fraction shorting (FS) and significantly decreased the left ventricular end-systolic diameter and left ventricular end-diastolic diameter at 28 days postmyocardial infraction (P < .05 for all). After MI, the ventricular repolarization duration, such as QTc intervals and action potential duration (APD) at 90% repolarization, was prolonged, and this prolongation could be decreased by CST (P < .05 for all). The CST also increased the threshold of ADP alternans (P < .01). Moreover, ventricular arrhythmias were induced in 83% of the MI group but only 33% of the MI + CST group (P < .05). These results suggested that the chronic administration of CST plays a role in cardioprotection in MI rats, which may function by decreasing the cardiac sympathetic drive and improving autonomic function.
© The Author(s) 2016.

Entities:  

Keywords:  autonomic function; cardiac function; catestatin; myocardial infarction; ventricular arrhythmia

Mesh:

Substances:

Year:  2016        PMID: 26821570     DOI: 10.1177/1074248416628676

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol Ther        ISSN: 1074-2484            Impact factor:   2.457


  13 in total

Review 1.  The role of neuropeptides in adverse myocardial remodeling and heart failure.

Authors:  Alexander Widiapradja; Prasad Chunduri; Scott P Levick
Journal:  Cell Mol Life Sci       Date:  2017-01-17       Impact factor: 9.261

2.  Identification of novel loci affecting circulating chromogranins and related peptides.

Authors:  Beben Benyamin; Adam X Maihofer; Andrew J Schork; Bruce A Hamilton; Fangwen Rao; Geert W Schmid-Schönbein; Kuixing Zhang; Manjula Mahata; Mats Stridsberg; Nicholas J Schork; Nilima Biswas; Vivian Y Hook; Zhiyun Wei; Grant W Montgomery; Nicholas G Martin; Caroline M Nievergelt; John B Whitfield; Daniel T O'Connor
Journal:  Hum Mol Genet       Date:  2017-01-01       Impact factor: 6.150

3.  MicroRNA-155 inhibition attenuates myocardial infarction-induced connexin 43 degradation in cardiomyocytes by reducing pro-inflammatory macrophage activation.

Authors:  Hai-Tao Yang; Li-Li Li; Song-Nan Li; Jin-Tao Wu; Ke Chen; Wei-Feng Song; Guo-Bao Zhang; Ji-Fang Ma; Hai-Xia Fu; Sheng Cao; Chuan-Yu Gao; Juan Hu
Journal:  Cardiovasc Diagn Ther       Date:  2022-06

4.  Catestatin reverses the hypertrophic effects of norepinephrine in H9c2 cardiac myoblasts by modulating the adrenergic signaling.

Authors:  Md Jahangir Alam; Richa Gupta; Nitish R Mahapatra; Shyamal K Goswami
Journal:  Mol Cell Biochem       Date:  2019-12-02       Impact factor: 3.396

Review 5.  Circulating chromogranin A and its fragments as diagnostic and prognostic disease markers.

Authors:  Angelo Corti; Fabrizio Marcucci; Tiziana Bachetti
Journal:  Pflugers Arch       Date:  2017-10-10       Impact factor: 3.657

6.  Abrogation of CC chemokine receptor 9 ameliorates ventricular remodeling in mice after myocardial infarction.

Authors:  Yan Huang; Dandan Wang; Xin Wang; Yijie Zhang; Tao Liu; Yuting Chen; Yanhong Tang; Teng Wang; Dan Hu; Congxin Huang
Journal:  Sci Rep       Date:  2016-09-02       Impact factor: 4.379

7.  CaMKII Activation Promotes Cardiac Electrical Remodeling and Increases the Susceptibility to Arrhythmia Induction in High-fat Diet-Fed Mice With Hyperlipidemia Conditions.

Authors:  Peng Zhong; Dajun Quan; Yan Huang; He Huang
Journal:  J Cardiovasc Pharmacol       Date:  2017-10       Impact factor: 3.105

Review 8.  The Association of Autonomic Nervous System Function With Ischemic Stroke, and Treatment Strategies.

Authors:  Mengxi Zhao; Ling Guan; Yilong Wang
Journal:  Front Neurol       Date:  2020-01-22       Impact factor: 4.003

9.  Distinct features of calcium handling and β-adrenergic sensitivity in heart failure with preserved versus reduced ejection fraction.

Authors:  Peter J Kilfoil; Sabine Lotteau; Rui Zhang; Xin Yue; Stephan Aynaszyan; Ryan E Solymani; Eugenio Cingolani; Eduardo Marbán; Joshua I Goldhaber
Journal:  J Physiol       Date:  2020-09-09       Impact factor: 5.182

10.  Circulating sST2 and catestatin levels in patients with acute worsening of heart failure: a report from the CATSTAT-HF study.

Authors:  Josip A Borovac; Duska Glavas; Zora Susilovic Grabovac; Daniela Supe Domic; Lada Stanisic; Domenico D'Amario; Chun S Kwok; Josko Bozic
Journal:  ESC Heart Fail       Date:  2020-07-18
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.