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作 者:应磊[1,2] 姚海霞[3] 黄林静[1] 马迎春[1] 何金波[1] 陈丹[1] 陈海娥[1] 汪洋[1,2] 王万铁[1,2]
机构地区:[1]温州医科大学基础医学院病理生理学教研室,温州325035 [2]温州医科大学缺血再灌注损伤研究所,温州325035 [3]上海市第六人民医院麻醉科,上海200233
出 处:《生理学报》2014年第2期203-209,共7页Acta Physiologica Sinica
基 金:supported by the Program of Foreign Cooperation in Science and Technology of Wenzhou Municipality of Zhejiang Province;China(No.HZ0090066)
摘 要:本文旨在探讨钙激活性氯离子通道(ClCa)在二级肺动脉血管低氧性肺血管收缩(hypoxic pulmonary vasoconstriction,HPV)中的作用。分离Sprague-Dawley(SD)雄性大鼠二级肺动脉血管,采用离体血管灌流法记录血管环张力变化。结果显示,常氧条件下,ClCa抑制剂尼氟灭酸(10和50μmol/L)和IAA-94(10μmol/L)使去甲肾上腺素收缩的二级肺动脉环血管产生明显的舒张反应(P<0.01),但对KCl收缩的二级肺动脉环血管并无影响。低氧条件下1 h内,去甲肾上腺素预收缩的二级肺动脉血管环出现双相性HPV反应,KCl预收缩的血管环无双相性收缩反应。尼氟灭酸和IAA-9明显减弱II期收缩反应(均P<0.01),对I期舒张反应也有显著减弱作用(均P<0.01),但对I期收缩几乎无影响。以上结果提示,ClCa是二级肺动脉血管双相性收缩反应II期收缩形成的一个重要因素,而在I期收缩中无明显作用。The aim of the present study was to investigate the roles of calcium-activated chloride channels (Clca) in the two- phase hypoxic pulmonary vasoconstriction (HPV). The second pulmonary artery branches were dissected from male Sprague-Dawley rats, and the changes in vascular tone were measured by using routine blood vascular perfusion in vitro. The result showed that, under normoxic conditions, Clca inhibitors (NFA and IAA-94) significantly relaxed second pulmonary artery contracted by norepinephrine (P 〈 0.01), but merely had effects on KCl-induced second pulmonary artery contractions. A biphasic contraction response was induced in second pulmonary artery ring pre-contracted with norepinephrine exposed to hypoxic conditions for at least one hour, but no biphasic contraction was observed in pulmonary rings pre-contracted with KC1. NFA and IAA-94 significantly attenuated phase II sustained hypoxic contraction (P 〈 0.01), and also attenuated phase I vasodilation, but had little effect on phase I contraction. These results sug- gest that Clca is an important component forming phase II contraction in secondary pulmonary artery, but not involved in phase I con- traction.
分 类 号:R543.2[医药卫生—心血管疾病]
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