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中国临床药理学与治疗学 ›› 1999, Vol. 4 ›› Issue (2): 140-143.

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利多卡因、异丙酚对缺血再灌注心肌细胞膜Na+-K+-ATP酶、肌浆网Ca2+-ATP酶活性的影响1

刘红亮, 戴体俊, 王钧, 曾因明   

  1. 徐州医学院麻醉医学研究所, 徐州 221002
  • 收稿日期:1999-04-14 出版日期:1999-06-26 发布日期:2020-12-04
  • 作者简介:刘红亮,男,24岁,硕士研究生。曾因明,男,65岁,教授,博士生导师,主要从事麻醉医学研究。
  • 基金资助:
    1 卫生部科研基金资助课题(No H9602)

Effects of lidocaine and propofol on the activities of myocardial sarcolemmal Na+-K+-ATP ase and sarcoplasic reticulum Ca2+-ATPase following ischemia-reperfusion

LIU Hong-Liang, DAiti-Jun, WANG Jun, ZEN Yin-Ming   

  1. Medical Institute of A neathesia, XuZhou Medical College, XuZhou 221002
  • Received:1999-04-14 Online:1999-06-26 Published:2020-12-04

摘要: 目的 观察利多卡因、异丙酚对缺血再灌注心肌细胞膜Na+-K+-ATP 酶、肌浆网Ca2+-ATP 酶活性的影响。方法 SD 大鼠48 只, 随机均分为6 组。假手术组;生理盐水组;利多卡因5 mg·kg-1 组;利多卡因10 mg·kg-1 组;异丙酚300 μg·kg-1·min-1组;异丙酚1000 μg·kg-1·min-1组。于缺血前5 min, 生理盐水及利多卡因经股静脉注射给药(30 s内注射完);异丙酚持续输注至缺血开始时为止。结扎冠脉左前降支, 造成左室前壁相应心肌组织缺血15 min, 然后松开结扎线再灌注10 min, 应用分光光度法测定心肌细胞膜Na+-K+-ATP酶、肌浆网Ca2+-ATP酶活性。结果 利多卡因可明显地促进肌浆网Ca2+-A TP酶活性的恢复(P<0.05), 大剂量时还促进心肌细胞膜Na+-K+-ATP酶活性的恢复(P<0.05)。异丙酚可显著地促进心肌细胞膜Na+-K+-ATP 酶活性的恢复(P<0.05, P<0.001), 大剂量时促进肌浆网Ca2+-ATP酶活性的恢复(P<0.05)。结论 利多卡因、异丙酚可促进再灌注期间心肌细胞膜Na+-K+-ATP 和肌浆网Ca2+-ATP酶活性的恢复, 从而抑制钙超载而减轻心肌缺血再灌注损伤。

关键词: 利多卡因, 异丙酚, 细胞膜Na+-K+-ATP酶, 肌浆网Ca2+-ATP, 缺血再灌注/心肌

Abstract: Aim To investigate the effects of lidocaine and propofol on the activities of myocardial sarcolemmal Na+-K+-ATPase and SR Ca2+-ATPase following ischemia-reperfusion. Methods forty-eight rats were randomly divided into six groups:Sham group(the coronary was not sutured), NS group (saline 5 ml·kg-1), L5 group (lidocaine 5 mg·kg-1), L10 group (lidocain 10 mg·kg-1), P300 group (propofol 300 μg·kg-1·min-1)and P1000 group (propofol 1000 μg·kg-1·min-1).Five minutes before ischemia, Saline or lidocaine was injected intrav eneously within 30 seconds and propofol was infused intraveneously till the onset of ischemia.The left coronary artery was occluded with a silk suture for fifteen minutes, then loosened to achieve reperfusion for ten minutes.The activities of sarcolemmal Na+-K+-AT Pase and SR Ca2+-A TPase were measured with pho to colorme-t re.Results Compared with that in NS group the activ ities of S R Ca2+-A TPase in the lido caine groups were increased significantly (P<0.05), while the activites of sarco lemmal Na+-K+-A TPase in propofol groups were increased significantly(P<0.05, P<0.01 respectively).Propofol of 1000 μg·kg-1·min-1 could increase the activity of SR Ca2+-ATPase (P<0.05).Lidocaine of 10 ml·kg-1 could increase the activity of sa rco lemmal Na+-K+-ATP ase significantly (P<0.05). Conclusion Lido caine, propofol could attenuate my ocardial ischemia-reperfusion injury by increasing the activities of sarcolemmal Na+-K+-ATPase and SR Ca2+-AT Pase during reperfusion.

Key words: lidocaine, propofol, sarcolemma Na+-K+-AT Pase, sarco plasic reticulum Ca2+-ATPase, ischemia-reperfusion/myocardium

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