Lai Xin, Zhong Liang, Fu Hai-Xia, Dang Song, Wang Xin, Zhang Ning, Feng Gao-Ke, Liu Zi-Qiang, Wang Xi, Wang Long
Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province; Cardiovascular Research Institute, Wuhan University, Wuhan, Hubei Province; Hubei Key Laboratory of Cardiology, Wuhan, Hubei Province, China.
Wuhan Medical & Healthcare Center for Women and Children, Wuhan, Hubei Province, China.
Neural Regen Res. 2017 Nov;12(11):1905-1910. doi: 10.4103/1673-5374.219054.
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 ischemic 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.
交感神经和迷走神经重塑在心肌梗死后的心功能中起重要作用。越来越多的证据表明,神经调节蛋白-1(NRG-1)可改善心力衰竭后的心脏功能。由于其对心肌梗死后心脏功能和神经重塑的影响尚不清楚,我们旨在研究NRG-1在心肌梗死后自主神经系统重塑中的作用。45只Sprague-Dawley大鼠被平均随机分为三组:假手术组(暴露左冠状动脉前降支但不结扎)、心肌梗死组(结扎左冠状动脉前降支)和心肌梗死加NRG-1组(结扎左冠状动脉前降支后腹腔注射NRG-1(10μg/kg,每日一次,共7天))。心肌梗死后4周,通过测量左心室收缩末期内径、左心室舒张内径、左心室收缩末期容积、左心室舒张末期容积、左心室射血分数和左心室缩短分数,用超声心动图检测大鼠心脏功能。通过实时PCR和蛋白质印迹法检测缺血心肌中酪氨酸羟化酶、生长相关蛋白-43(神经元特异性蛋白)、神经生长因子、胆碱乙酰转移酶(迷走神经标志物)和囊泡乙酰胆碱转运体(心脏迷走神经纤维标志物)的mRNA和蛋白表达水平,以评估自主神经重塑。心肌梗死后,大鼠心脏功能显著恶化,注射NRG-1后明显改善。与心肌梗死组相比,心肌梗死加NRG-1组酪氨酸羟化酶和生长相关蛋白-43的mRNA和蛋白水平以及胆碱乙酰转移酶mRNA水平显著降低,而神经生长因子和囊泡乙酰胆碱转运体的mRNA和蛋白水平以及胆碱乙酰转移酶蛋白水平略有降低。我们的结果表明,NRG-1可改善心肌梗死后的心脏功能并调节交感神经和迷走神经重塑,从而达到自主神经系统的新平衡以保护心脏免受损伤。