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超极化停搏对体外循环中心肌组织磷酯酶A2及ATPase活性的影响
引用本文:曾志勇,杨胜生,庄聪文,程先进,黄盛东,徐志云. 超极化停搏对体外循环中心肌组织磷酯酶A2及ATPase活性的影响[J]. 中国现代医学杂志, 2007, 17(21): 2589-2592
作者姓名:曾志勇  杨胜生  庄聪文  程先进  黄盛东  徐志云
作者单位:1. 南京军区福州总医院,心胸外科,福建,福州,350025
2. 第二军医大学长海医院,胸心外科,上海,200433
摘    要:目的观察超极化停搏(超极化停搏)对体外循环中缺血再灌注心肌组织磷酯酶A2(PLA2)和ATPase活性的影响,评价其对心肌的保护作用,并初步探讨其可能的作用机制。方法在猫体外循环模型的基础上,比较超极化停搏组和去极化停搏组体外循环中心肌组织PLA2及Na -K -ATPase、Ca2 -Mg2 -ATPase和Ca2 -ATPase活性。结果超极化停搏处理组可明显减轻体外循环中缺血再灌注导致的PLA2活性升高和ATPase活性下降。结论超极化停搏可能通过减轻缺血再灌注期间的Ca2 超载及抑制细胞膜磷脂水解而发挥其心肌保护作用。

关 键 词:体外循环  心肌再灌注损伤  磷酯酶  ATP酶  超极化停搏
文章编号:1005-8982(2007)21-2589-04
收稿时间:2007-05-10
修稿时间:2007-05-10

Effect of hyperpolarized arrest on activities of phospholipase A2 and ATPase of myocardial cells during cardiopulmonary bypass
ZENG Zhi-yong,YANG Sheng-sheng,ZHUANG Cong-wen,CHENG Xian-jin,Huang Sheng-dong,XU Zhi-yun. Effect of hyperpolarized arrest on activities of phospholipase A2 and ATPase of myocardial cells during cardiopulmonary bypass[J]. China Journal of Modern Medicine, 2007, 17(21): 2589-2592
Authors:ZENG Zhi-yong  YANG Sheng-sheng  ZHUANG Cong-wen  CHENG Xian-jin  Huang Sheng-dong  XU Zhi-yun
Abstract:[Objective] To elucidate the influences of hyperpolarized arrest on activity of phospholipase A2 and ATPase of ischemia/reperfusion myocardial cell during cardiopulmonary bypass(CPB). [Methods] Seventy-five felines were randomized into three groups: simply CPB group, depolarized arrest group and hyperpolarized arrest group. In simple CPB group, CPB was conducted without aortic cross-clamping (ACC). In depolarized arrest group and hyperpolarized arrest group, hearts underwent 60 minutes of global ischemia after ACC and infusion of cardioplegic solution (10 mL/kg), followed by 90 minutes of reperfusion. The cardioplegic solution consisted of St. Thomas solution with KCl (16 mmol/L) in depolarized arrest group or pinacidil (50 mmol/L) in hyperpolarized arrest group. Activities of PLA2 and Na -K- ATPase, Ca2 -Mg2 -ATPase and Ca2 -ATPase of myocardial cells were simultaneously measured during ACC and reperfusion periods. [Results] Hyperpolarized arrest significantly alleviated the upregulated activity of PLA2 and the inhibited activities of Na -K- ATPase, Ca2 -Mg2 -ATPase and Ca2 -ATPase of myocardium during periods of ischemia and reperfusion. [Conlusion] Hyperpolarized arrest can protect myocardial cells from ischemia and reperfusion injury during CPB by regulating the activities of PLA2 and the ATPases of myocardium, which may duo to alleviation of Ca2 overload and hydrolysis of membrane phospholipid.
Keywords:cardiopulmonary bypass  myocardial reperfusion injury  phospholipase  ATPase  hyperpolarized arrest
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