Dong Deli

Cardioprotective effects and underlying mechanisms of oxymatrine against Ischemic myocardial injuries of rats.

Oxymatrine has been demonstrated to have a variety of pharmacological actions. Accumulating evidence indicates that oxymatrine may exert a protective effect on the cardiovascular system. The study was designed to explore the possible role of oxymatrine against myocardial ischemic damage and several related signaling pathways as potential mechanisms. The protective properties of oxymatrine were studied in a rat model of acute myocardial infarction due to permanent ligation of the left anterior descending coronary artery. The results showed that administration of oxymatrine relieved myocardial injuries during ischemia, and this was achieved by protecting cardiomyocytes from apoptotic death. The beneficial effects of oxymatrine were likely mediated by an inhibition of lipid peroxidation (MDA production) and an increase in endogenous antioxidant activity (SOD), activation of the survival signaling molecule (Bcl‐2), and a reduction of apoptotic mediator (Fas) and intracellular Ca2+ overload. Copyright

Ketamine-induced ventricular structural, sympathetic and electrophysiologic remodelling: pathological consequences and protective effects of metoprolol

Purpose Growing evidence suggested long-term abuse of ketamine did harm to the heart and increased the risk of sudden death. The present study was performed to explore the cardiotoxicity of ketamine and the protective effects of metoprolol. Methods Rats and rabbits were divided into control, ketamine poisoning and ketamine plus metoprolol groups. Ketamine (40 mg/kg/day, intraperitoneally) and metoprolol (20 mg/kg/day, orally) were administered continuously for 12 (rats) or eight (rabbits) weeks, respectively. Cardiac function and electrophysiological disturbances were examined, collagen volume fraction and apoptotic cell number were analysed and remodelling related proteins were detected by immunohistochemistry and western blot. Results Rabbits showed decreased left ventricular ejection fraction, slowed ventricular conduction velocity, and increased susceptibility to ventricular arrhythmia. Metoprolol prevented these pathophysiological alterations. In ketamine-treated rats, cardiac collagen volume fraction and apoptotic cell number were much higher than normal, which were mitigated by co-administration of metoprolol. Consistently, the expressions of poly (ADP-ribose) polymerases-1, apoptosis inducing factor and nuclear factor kappa-light-chain-enhancer of activated B cells were all increased after ketamine treatment, and sharply reduced after metoprolol administration. Moreover, ketamine enhanced sympathetic sprouting manifested by increased growth-associated protein 43 and tyrosine hydroxylase expression, which were also prevented by metoprolol. Conclusion Long-term abuse of ketamine caused significant ventricular myocardial apoptosis, fibrosis and sympathetic sprout, which altered the electrophysiologic property of the heart and increased the susceptibility to malignant arrhythmia that may lead to sudden cardiac death. Metoprolol prevented the cardiotoxicity of ketamine, representing a promising therapeutic strategy.