Abstract

BackgroundMyocardial apoptosis is important in the pathogenesis and progression of myocardial infarction-induced heart failure (MI-HF). Renal sympathetic denervation (RDN) has become a promising therapeutic strategy for the treatment of HF. Previous studies have shown that RDN could improve heart function Yao et al. (Exp Ther Med 14:4104-4110, 2017). However, whether and how RDN regulates myocardial apoptosis in MI-HF is unclear. This study sought to evaluate the effects of RDN on cardiac function and apoptosis-related gene expression in MI-HF dogs.MethodsEighteen healthy mongrel dogs were randomly divided into control group(n = 6), model group(n = 6) and treatment group(n = 6). MI-HF was established in model group and treatment group by anhydrous alcohol embolization, after heart failure dogs in the treatment group and model group proceeded bilateral renal artery ablation and bilateral renal arteriography, respectively. The cardiac function parameters were evaluated by echocardiographic; the serum NT-BNP level was detected by ELISA; the degree of myocardial fibrosis was observed through masson staining; the expression of MMP-2, MMP-9 in the cardiac were got by immunohistochemistry. TUNEL method was used to observe cardiomyocyte apoptotsis and calculate the apoptosis index (AI). Relative expression of Bcl-2 and Bax, Caspase3 and GRP78 were detected using RT-PCR and Western Blot. Renal artery H&E staining and serum creatinine were conducted to access the efficacy and safety of RDN.ResultsFour weeks after RDN, the LVEDD, LVESD and LVEDP decreased, and the LVEF and LVSP increased in the treatment group compared with those in the control group (all P < 0.05). Moreover, NT-BNP, an indicator of cardiac function was decreased. Additionally, MMP-2 and MMP-9 levels in the myocardium decreased significantly in the treatment group. Furthermore, the levels of Bax, and caspase 3 decreased, while the level of Bcl-2 increased. Thus, myocardial apoptosis was attenuated in RDN treated dogs. We also found that the level of GRP78 which is activated in response to endoplasmic reticulum (ER) stress, was decreased. However, serum creatinine levels were not significantly different between the RND-treated dogs and the control dogs.ConclusionCardiac function was improved by RDN treatment through regulating apoptosis and ER stress in cardiomyocytes in dogs after MI.

Highlights

  • Myocardial apoptosis is important in the pathogenesis and progression of myocardial infarctioninduced heart failure (MI-Heart failure (HF))

  • One dog in the treatment group died 1 day after acute myocardial infarction (AMI) because of ventricular fibrillation, and one dog in the model group died of HF 30 days after AMI; there were no deaths in the normal group

  • Previous study demonstrated that Renal sympathetic denervation (RDN) leads to a significant improvement of cardiac function by shifting cardiac apoptosis to autophagy in diabetic rabbits [13].Another study showed that RDN could decrease cardiomyocyte apoptosis in canines with prolonged atrial pacing [14]

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Summary

Introduction

Myocardial apoptosis is important in the pathogenesis and progression of myocardial infarctioninduced heart failure (MI-HF). Previous studies have shown that RDN could improve heart function Yao et al (Exp Ther Med 14: 4104-4110, 2017). Whether and how RDN regulates myocardial apoptosis in MI-HF is unclear. This study sought to evaluate the effects of RDN on cardiac function and apoptosis-related gene expression in MI-HF dogs. Heart failure (HF) is a common complication of acute myocardial infarction (AMI) and is characterized by cardiac dysfunction along with autonomic imbalance. Myocardial apoptosis is important in the pathogenesis and progression of MI-induced HF. The local adverse stimulus after MI induces myocyte apoptosis [2] and promotes the deterioration of cardiac function and ventricular remodeling. Loss of myocardial cells is associated with impaired heart function

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