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作 者:周俐[1] 汪秀荣[2] 周青[2] 何蔚[1] 连其深[1]
机构地区:[1]赣南医学院药理教研室,赣州341000 [2]赣南医学院机能实验室,赣州341000
出 处:《中药药理与临床》2007年第3期44-46,共3页Pharmacology and Clinics of Chinese Materia Medica
摘 要:目的:研究血塞通注射液(Xuesaitong Injection,XST)对异丙肾上腺素致大鼠心肌肥厚的保护作用及对氧化应激的影响。方法:采用异丙肾上腺素(isoproterenol,ISO)5mg/kg·dsc连续7d。诱导大鼠心肌肥厚模型。大鼠随机分为NS对照组、ISO模型组、XST(25、50mg/kg)治疗组。测定全心重量指数(HW/BW),左心室重量指数(LVW/BW即LVI);采用分光光度法检测左心室心肌组织中羟脯氨酸(Hyp)和丙二醛(MDA)的含量,超氧化物歧化酶(SOD)、谷胱苷肽过氧化物酶(GSH-Px)的活力以及血清中超氧化物歧化酶(SOD)活力、磷酸肌酸激酶(CK)和丙二醛(MDA)含量的变化。结果:ISO模型组大鼠的心脏重量指数明显增大,左心室Hyp、MDA含量增高,SOD、GSH-Px活力显著下降;血清MDA、CK水平明显升高,SOD活力明显下降。PNS能明显降低血清中CK的释放,降低血清和心肌中MDA水平及提高SOD活力,保护心肌组织GSH-Px酶活性,减少心肌组织胶原的含量,减轻心脏重量指数,抑制心肌肥厚。结论:XST对ISO所致大鼠心肌肥厚具有一定的保护作用,其机制可能与抗氧化作用有关。Object: To investigate the antioxidative effects of Xuesaitong injection(XST) on myocardial hypertrophy induced by isoproterenol (ISO) in rats. Methods: Myocardial hypertrophy model of rats were induced by injection of ISO (5 mg/kg·d,sc) for 7d. Rats were rabdomly divided into NS control group , ISO model group and two XST groups (25,50 mg/kg). Then, the myocardial indexes were measured;the hydroxyroline and malondialdehde (MDA) content of left ventricle,the activity of superoxide dismutase (SOD) and glutathione peroxidase ( GSH - Px) in left ventricle were determined ; the activity of SOD , the levels of CK, MDA in serum were measured by spectrophotometry respectively. Results: In ISO model group ,the myocardial indexes and the content of hydroxyproline and MDA in left ventricle markedly increased; the activilty of SOD and GSH- Px in left ventricle were decreased; the content of MDA and CK in serum markedly increased; the activihy of SOD in serum were decreased. Treatment with XST significantly reduced the myocardial indexes and the hydroxyproline and MDA content, increased the activity of SOD and GSH- Px in heart tissue; increased the activity of SOD, significantly reduced the MDA and CK content in serum. Conclusion: XST was shown to prevent remodeling of myocardial hypertrophy induced by ISO in rats ; The effect of XST on anti -hypertrophy was associated with inhibiting oxidative response.
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