Neural Regeneration Research ›› 2017, Vol. 12 ›› Issue (11): 1905-1910.doi: 10.4103/1673-5374.219054

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Effects of neuregulin-1 on autonomic nervous system remodeling post-myocardial infarction in a rat model

Xin Lai1, 2, 3, Liang Zhong4, Hai-xia Fu5, Song Dang1, 2, 3, Xin Wang1, 2, 3, Ning Zhang1, 2, 3, Gao-ke Feng1, 2, 3, Zi-qiang Liu1, 2, 3, Xi Wang1, 2, 3, Long Wang2, 3   

  1. 1 Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China
    2 Cardiovascular Research Institute, Wuhan University, Wuhan, Hubei Province, China
    3 Hubei Key Laboratory of Cardiology, Wuhan, Hubei Province, China
    4 Wuhan Medical & Healthcare Center for Women and Children, Wuhan, Hubei Province, China
    5 Department of Cardiology, Henan Province People’s Hospital, Zhengzhou, Henan Province, China
  • Received:2017-06-27 Online:2017-11-15 Published:2017-11-15
  • Contact: Xi Wang, M.D., Ph.D. or Long Wang, M.D., Ph.D.,xiwangwhu@163.com or wanglongwhu@163.com.
  • Supported by:

    This work was supported by a grant from the National Key Basic Research Development Program, the “973” Program, No.2012CB518604; the National Natural Science Foundation of China, No. 81260052; the Natural Science Foundation of Hubei Province, No.2014CKB497, 2014BKB075, and 2015BKA339; and the Natural Science Foundation of Henan Province of China, No. 201602262.

Abstract:

Sympathetic nerve and vagus nerve remodeling play an important part in cardiac function post-myocardial infarction (MI). Increasing evidence indicates that neuregulin-1 (NRG-1) improves cardiac function following heart failure. Since its impact on cardiac function and neural remodeling post-MI is poorly understood, we aimed to investigate the role of NRG-1 in autonomic nervous system remodeling post-MI. Forty-five Sprague-Dawley rats were equally randomized into three groups: sham (with the left anterior descending coronary artery exposed but without ligation), MI (left anterior descending coronary artery ligation), and MI plus NRG-1 (left anterior descending coronary artery ligation followed by intraperitoneal injection of NRG-1 (10 μg/kg, once daily for 7 days)). At 4 weeks after MI, echocardiography was used to detect the rat cardiac function by measuring the left ventricular end-systolic inner diameter, left ventricular diastolic diameter, left ventricular end-systolic volume, left ventricular end-diastolic volume, left ventricular ejection fraction, and left ventricular fractional shortening. mRNA and protein expression levels of tyrosine hydroxylase, growth associated protein-43 (neuronal specific protein),nerve growth factor, choline acetyltransferase (vagus nerve marker), and vesicular acetylcholine transporter (cardiac vagal nerve fiber marker) in ischem ic myocardia were detected by real-time PCR and western blot assay to assess autonomous nervous remodeling.
After MI, the rat cardiac function deteriorated significantly, and it was significantly improved after NRG-1 injection. Compared with the MI group, mRNA and protein levels of tyrosine hydroxylase and growth associated protein-43, as well as choline acetyltransferase mRNA level significantly decreased in the MI plus NRG-1 group, while mRNA and protein levels of nerve growth factor and vesicular acetylcholine transporters, as well as choline acetyltransferase protein level slightly decreased. Our results indicate that NRG-1 can improve cardiac function and regulate sympathetic and vagus nerve remodeling post-MI, thus reaching a new balance of the autonomic nervous system to protect the heart from injury.

Key words: nerve remodeling, myocardial infarction, neuregulin-1, sympathetic nerve, vagus nerve, animal model, real-time PCR, western blot assay, cardiac function, echocardiography