检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:吴茂旺[1] 朱建华[1] 张德雨[1] 朱少华[2] 刘良[2] 黄光照[2]
机构地区:[1]皖南医学院法医学系,安徽芜湖241001 [2]华中科技大学同济医学院法医学系,湖北武汉430030
出 处:《中国法医学杂志》2008年第3期154-156,I0002,共4页Chinese Journal of Forensic Medicine
基 金:安徽省教育厅自然科学基金资助项目(K80143)
摘 要:目的探讨博落回对心肌作用的机制。方法SD大鼠36只分为2个实验组和1个对照组,每组12只;2个实验组分别按1/6LD50、1/3LD50剂量的博落回水煎液灌胃,对照组以蒸馏水灌胃。各组大鼠处死后,每组10只取心肌组织制成匀浆,检测Ca2+.Mg2+-ATPase与SDH(琥珀酸脱氢酶)的活性;另2只大鼠心肌行超微结构观察。结果1/6LD50组大鼠心肌内Ca2+.Mg2+-ATPase与SDH活性较对照组有显著性升高(P<0.05);1/3 LD50组大鼠心肌内Ca2+.Mg2+-ATPase与SDH活性同对照组比较无显著性差异(P>0.05),但呈下降趋势。超微结构观察到实验组大鼠心肌细胞发生凋亡及1/3 LD50组大鼠出现心肌排列紊乱、断裂等征象。结论博落回对大鼠心肌内Ca2+.Mg2+-ATPase与SDH的活性有影响作用,并能诱导心肌细胞凋亡。Objective To study the mechanism of the rat's myocardium induced by macleaya cordata. Methods 36 SD rats were randomly assigned to 2 experimental groups treated by macleaya cordata decoction with a dose of 1/6 LD50, 1/3 LD50 respectively and a control group treated with distilled water by oral administration. The rats were killed 6 hours after the administration for taking the cardiac muscle to examine the Ca2+.Mg2+-ATPase, SDH while observing the structures. Resoults In the group treated by macleaya cordata with dose of 1/6 LD50, the activity of Ca2+.Mg2+-ATPase and SDH were increased significantly. However, the groups treated by macleaya cordata with dose of 1/3 LD50 and distilled water, the activity of Ca2+.Mg2+-ATPase, SDH showed no significant observed in the experimental groups, while the change. changes The apoptosise in myocardium cells of rat's can be were not seen in control group. Conclusion The results indicate that the macleaye cordata can induce and improve the apoptosis of myocardium cells in low dose, and these effects may be induced by stimulating the activity of Ca2+.Mg2+-ATPase, SDH in myocardium cells.
关 键 词:法医病理学 博落回 Ca2+.Mg2+-ATPase SDH 细胞凋亡
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.229