Therapeutic effect of neuregulin-1β on pressure overload-induced myocardial hypertrophy in rats

AIM: To investigate the therapeutic effect and the mechanism of neuregulin-1β(NRG-1β) on the rat model of myocardial hypertrophy induced by pressure overload.METHODS: Eight weeks after coarctation of abdominal aorta,the Wistar rats were randomly divided into 4 groups: myocardial hypertrophy(model) group,sham operation(sham) group,NRG-1β treatment group(intravenous injection of NRG-1β at dose of 10 μg/kg daily for 7 d) and NRG-1β+Herceptin(HERCE) treatment group [intravenous injection of NRG-1β(10 μg/kg) plus HERCE(10 μg/kg) daily for 7 d].The characteristics of heart functions were evaluated by the methods of hemodynamics and echocardiography.Masson staining was employed to observe the pathological changes of myocardial tissues.The concentration of angiotensin II(Ang II) in myocardial tissues was measured by radioimmunoassay.The level of tumor necrosis factor α(TNF-α) in myocardial tissues was detected by ELISA.The mRNA expression of B-cell lymphoma/leukemia-2(bcl-2) and bcl-2-associated X protein(bax) in the myocardium was determined by RT-PCR.RESULTS: The left ventricular ejection fraction(LVEF) and left ventricular fraction shortening(LVFS) were higher,while the left ventricular end-systolic diameter(LVESD) and left ventricular end-diastolic diameter(LVEDD) were smaller in NRG-1β group than those in model group.The left ventricular end-systolic pressure(LVESP) and maximal rate of increase/decrease in left ventricular pressure(±dp/dtmax) were higher,and left ventricular end-diastolic pressure(LVEDP) was significantly lower in NRG-1β group than those in model group.Compared with model group,treatment with NRG-1β decreased collagen volume fraction(CVF),reduced the Ang II and TNF-α,increased bcl-2 mRNA expression,and decreased bax mRNA expression in myocardial tissues.No difference of the above parameters between model group and NRG-1β+HERCE treatment group was observed.CONCLUSION: NRG-1 reduces the expression of Ang II and TNF-α in myocardial tissues in pressure-overload rats,thus reducing Ang II and TNF-α mediated myocardial interstitial remodeling.Increase in the mRNA expression of bcl-2 and decrease in the mRNA expression of bax by NRG-1 inhibit myocardial cell apoptosis,which is responsible for its role of improving cardiac function of myocardial hypertrophy induced by pressure overload.