机构:[1]Department of Tumor Surgery, Wuwei Tumor Hospital, Wuwei, Gansu, PR China,[2]Department of Paediatrics, Changhai Hospital, Second Military Medical University, Shanghai, PR China,[3]International Medical Center, Chinese PLA General Hospital, Beijing, PR China,[4]Department of Tumor Chemotherapy, Wuwei Tumor Hospital, Wuwei, Gansu, PR China,[5]Research Center for Biochemistry and Molecular Biology, Jiangsu Key Laboratory of Brain Disease Bioinformation, Xuzhou Medical College, Xuzhou, Jiangsu, PR China,[6]Department of Cardiology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, PR China
Context: The serious side effect of Adriamycin (ADR) is cardiomyopathy. Cryptotanshinone (CRY) is widely and safely used as antioxidant with MTD more than 5mg/g in rats (p.o).Objective: The objective of this study is to study the protection effects of CRY against ADR-induced mitochondrial dysfunction in cardiomyocytes.Materials and methods: The chemical administration lasted for 20 days with an effective dose of CRY (p.o.) at 50 mg/kg in rats. Mitochondrial respiratory chain complex activities, ATP generation, mitochondrial membrane potential (MMP), superoxide anion free radical, oxidative stress-relative enzymes, and mitochondrial biogenesis-relative factors in normal control, ADR (i.p., 1.25mg/kg), and ADR (i.p., 1.25mg/kg)+CYP (p.o., 50mg/kg) groups were detected.Results: 50mg/kg CRY significantly promoted the energy production of ATP (16.992.38nmol/g Pro) (Pro: Protein) by increasing the complexes activities except II (p>0.05). After the treatment of CRY, the suppressed MMP was increased while superoxide anion free radical (0.57 +/- 0.07/mg Pro) was inhibited markedly. Mitochondrial biogenesis-relative factors PGC-1, NRF-1, and TFAM were also promoted. Remarkable augmentations of NO, inducible nitric oxide synthase (iNOS), and increased activity of GSH-PX (p<0.05) were also detected after the treatment of CRY, while no obvious changes on the activity of nitric oxide synthase (cNOS; p>0.05) were observed.Discussion and conclusion: These results suggest that CRY protects against ADR-induced mitochondrial dysfunction in cardiomyocytes. It could be an ideal potential drug of cardioprotection.
基金:
Research Program of Wuwei Tumor Hospital; Chinese PLA General Hospital