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:符云峰[1] 王素敏[1] 卢振敏[1] 李红[1]
出 处:《高血压杂志》1999年第2期125-127,共3页Chinese Journal of Hypertension
基 金:河北省自然科学基金
摘 要:目的探讨高血压时血浆胆固醇(Cho)、甘油三酯(TG)和高密度脂蛋白(HDL-C)水平与细胞膜离子运输酶活性之间的关系。方法32名正常人(NT),55例原发性高血压(HT)患者,检测血浆Cho、TG、HDL-C水平,红细胞膜Na+-K+-ATP酶和Ca2+-ATP酶活性,膜C/P克分子比率及膜内面Ca2+结合力。结果(1)HT组平均动脉血压(MAP)与NT组相比有显著性差别;(2)HT组血浆HDL-C水平、红细胞膜Na+-K+-ATP酶和Ca2+-ATP酶活性,以及膜内面Ca2+结合力均较NT组明显减低;(3)HT组血浆Cho,TG水平、红细胞膜Cho含量和C/P克分子比率,与NT组比较皆明显增高。结论红细胞膜Na+-K+-ATP酶和Ca2+-ATP酶活性减低,以及膜内面Ca2+结合力减低,是高血压时细胞膜离子运输失常的主要标志,血浆TG水平升高和膜磷脂水平减低可能是高血压时细胞膜理化特性及离子运输失常的主要决定因素。Aim \ To investigate the relationship between plasma cholesterol(Cho), triglycerides(TG)high density lipoprotein(HDL) and ion transport enzymes activities of red cell membranes in patients with essential hypertension.\ Methods \ Plasma ChTG,HDLC,activities of Na+K+ATPase and Ca2+ATPase,Ca2+binding capacity of membrane innersurface and membrane Cho, phospholipids(PL) were measured in 32 normotensive (NT) subjects, 55 patients with essential hypertension.\ Results \ (1)Mean artery pressure(MAP), plasma ChTG and membrane Cho levels, and membrane cholesterol/phospholipids(C/P)molar ratio are significantly increased when compared with those in NT group; (2)The plasma HDLC level and activities of Na+K+ATPase and Ca2+ATPase, and the inner surface Ca2+binding capacity in HT group are significantly decreased than those in NT group,respectively.\ Conclusion \ The depressed activities of Na+K+ATPase and Ca2+ATPase, the decreased innersurface Ca2+binding capacity of cell membranes are the major ions transport abnormalities in essential hypertension. The plasma TG and membrane C/P molar ratiodependent changes in membrane microviscosity seems to be responsible for the modulation of particular ion transport pathways.
分 类 号:R544.1[医药卫生—心血管疾病]
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