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Mechanisms underlying the cardioprotective effect of Salvianic acid A against isoproterenol-induced myocardial ischemia injury in rats: Possible involvement of L-type calcium channels and myocardial contractility

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机构: [1]Hebei Med Univ, 361 East Zhongshan Rd, Shijiazhuang 050017, Hebei, Peoples R China [2]Hebei Med Univ, Hosp 4, 12 Jiankang Rd, Shijiazhuang 050011, Hebei, Peoples R China [3]Hebei Univ Chinese Med, 3 Xingyuan Rd, Shijiazhuang 050200, Hebei, Peoples R China [4]China Pharmaceut Univ, Key Lab Drug Metab & Pharmacokinet, 1 Shennong Rd Cent Door, Nanjing 210038, Jiangsu, Peoples R China [5]Hebei Gen Hosp, Dept Infect Dis, Shijiazhuang 050051, Hebei, Peoples R China
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关键词: Radix Salviae Milthiorrhizae Salvianic acid A Isoproterenol Myocardial ischemia injury L-type calcium current Myocardial contractility

摘要:
Ethnopharmacological relevance: Salvianic acid A (SAA), which is the main water-soluble fraction in Radix Salviae Milthiorrhizae, has been widely applied for treating cardiovascular diseases in China. Aim of the study: To explore the effects of SAA against myocardial ischemia injury induced by isoproterenol (ISO) in rats and to clarify its underlying myocardial protective mechanisms based on L-type calcium channels and myocardial contractility. Materials and methods: The myocardial ischemia injured rat model was induced by administering ISO (85 mg/kg) subcutaneously at evenly spaced intervals throughout the day and night for 2 consecutive days. Serum cardiac biomarkers were analyzed, and heart tissues were isolated and prepared for histopathology assay. The regulatory effects of SAA on the L-type calcium current (ICa-L) in rat ventricular myocytes were observed by the patch clamp technique. The IonOptix Myocam detection system was used to observe the contractility of isolated rat ventricular myocytes. Results: SAA significantly ameliorated changes in heart morphology and electrocardiographic patterns and reduced serum levels of creatine kinase and lactate dehydrogenase in the ISO-induced myocardial ischemia injured rat model. Meanwhile, SAA reduced in a concentration-time dependent way with an IC50 of 1.47 x 10(-5) M, upshifted the current-voltage, activation, and inactivation curves of ICa-L, and significantly inhibited the amplitude of the cell shortening. Conclusions: These results indicate that SAA exhibits significant cardioprotective effects against the ISO induced myocardial ischemia injury, potentially through inhibiting ICa-L and decreasing myocardial contractility. (C) 2016 Elsevier Ireland Ltd. All rights reserved.

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出版当年[2016]版:
大类 | 3 区 医学
小类 | 2 区 全科医学与补充医学 2 区 植物科学 3 区 药物化学 3 区 药学
最新[2025]版:
大类 | 2 区 医学
小类 | 1 区 全科医学与补充医学 1 区 药学 2 区 药物化学 2 区 植物科学
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出版当年[2016]版:
Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Q1 PLANT SCIENCES Q2 CHEMISTRY, MEDICINAL Q2 PHARMACOLOGY & PHARMACY
最新[2024]版:
Q1 CHEMISTRY, MEDICINAL Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Q1 PHARMACOLOGY & PHARMACY Q1 PLANT SCIENCES

影响因子: 最新[2024版] 最新五年平均 出版当年[2016版] 出版当年五年平均 出版前一年[2015版] 出版后一年[2017版]

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第一作者机构: [1]Hebei Med Univ, 361 East Zhongshan Rd, Shijiazhuang 050017, Hebei, Peoples R China
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通讯机构: [1]Hebei Med Univ, 361 East Zhongshan Rd, Shijiazhuang 050017, Hebei, Peoples R China [3]Hebei Univ Chinese Med, 3 Xingyuan Rd, Shijiazhuang 050200, Hebei, Peoples R China [*1]Hebei Medical University, No.361, East Zhongshan Road, Shijiazhuang 050017, Hebei, China
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