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Cryptotanshinone protects against adriamycin-induced mitochondrial dysfunction in cardiomyocytes

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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
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关键词: ATP generation cardiovascular protection mitochondrial biogenesis mitochondrial complex activity mitochondrial membrane potential mitochondrial respiratory chain oxidative stress superoxide anion free radical

摘要:
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.

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出版当年[2015]版:
大类 | 4 区 医学
小类 | 4 区 医学实验技术 4 区 药学 4 区 植物科学
最新[2023]版:
大类 | 3 区 医学
小类 | 2 区 医学实验技术 2 区 药学 2 区 植物科学
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出版当年[2014]版:
Q3 PLANT SCIENCES Q3 MEDICAL LABORATORY TECHNOLOGY Q4 PHARMACOLOGY & PHARMACY
最新[2023]版:
Q1 MEDICAL LABORATORY TECHNOLOGY Q1 PLANT SCIENCES Q1 PHARMACOLOGY & PHARMACY

影响因子: 最新[2023版] 最新五年平均 出版当年[2014版] 出版当年五年平均 出版前一年[2013版] 出版后一年[2015版]

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第一作者机构: [1]Department of Tumor Surgery, Wuwei Tumor Hospital, Wuwei, Gansu, PR China,
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通讯机构: [3]International Medical Center, Chinese PLA General Hospital, Beijing, PR China,
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