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

机译:neuregulin-1对大鼠心肌梗死后自主神经系统重塑的影响

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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.
机译:交感神经和迷走神经重塑在心肌梗死(MI)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。由于对MI后心脏功能和神经重塑的影响了解甚少,因此我们旨在研究NRG-1在MI后自主神经系统重塑中的作用。将四十五只Sprague-Dawley大鼠随机分为三组:假手术(暴露左冠状动脉前降支但未结扎),MI(冠状动脉左前降支结扎)和MI加NRG-1(冠状动脉左前降支)结扎动脉,然后腹膜内注射NRG-1(10μg/ kg,每天一次,连续7天)。 MI后4周,超声心动图通过测量左心室收缩末期内径,左心室舒张末径,左心室收缩末期体积,左心室舒张末期体积,左心室射血分数,来检测大鼠心功能。和左心室分数缩短。真实地检测缺血性心肌中酪氨酸羟化酶,生长相关蛋白43(神经特异性蛋白),神经生长因子,胆碱乙酰转移酶(迷走神经标记)和囊泡乙酰胆碱转运子(心脏迷走神经纤维标记)的mRNA和蛋白表达水平。时PCR和Western印迹法评估自主神经重塑。 MI后,大鼠心脏功能明显恶化,注射NRG-1后大鼠的心脏功能明显改善。与MI组相比,MI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水平明显降低,而神经生长因子和水泡乙酰胆碱的mRNA和蛋白水平明显降低。转运蛋白以及胆碱乙酰转移酶的蛋白水平略有下降。我们的结果表明,NRG-1可以改善心肌梗死后的心脏功能并调节交感神经和迷走神经的重构,从而达到自主神经系统的新平衡,从而保护心脏免受伤害。

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