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中国临床药理学与治疗学 ›› 2000, Vol. 5 ›› Issue (4): 309-312.

• 论著 • 上一篇    下一篇

地氟醚、七氟醚和异氟醚预处理增加缺氧/复氧心肌细胞ATP的贮存

叶敏, 彭章龙1   

  1. 安徽医科大学附设护士学校, 合肥230032;1安徽医科大学第一附属医院
  • 收稿日期:2000-10-09 出版日期:2000-12-26 发布日期:2020-11-27
  • 作者简介:彭章龙,男,医学博士。

Preconditioning with desflurane, sevoflurane and isoflurane increase the preservation of adenosine triphosphate in anoxia-reoxygenation myocardial cells

YE Min, PENG Zhang-Long1   

  1. Nurse’s School;1First Affiliated Hospital, Anhui Medical University, Hefei 230032
  • Received:2000-10-09 Online:2000-12-26 Published:2020-11-27

摘要: 目的 研究地氟醚、七氟醚和异氟醚预处理对缺氧/复氧心肌细胞ATP含量影响及其与细胞损害的关系。方法 原代培养乳鼠心肌细胞随机分为对照、单纯缺氧/复氧及1.5 肺泡气最低有效浓度(MAC)地氟醚、七氟醚和异氟醚预处理5组。实验结束测定心肌细胞内ATP、心肌酶LDH和CK、细胞存活率。结果 1.5MAC地氟醚、七氟醚和异氟醚预处理显著减轻缺氧/复氧引起的ATP含量和细胞存活率下降,以及LDH和CK的升高;ATP含量变化与LDH和CK呈负相关(r分别为-0.87和-0.82,P<0.01),与细胞存活率呈正相关(r为0.83,P<0.01)。结论 地氟醚、七氟醚和异氟醚预处理可增加缺氧/复氧心肌细胞内ATP,是其心肌保护机制之一。

关键词: 挥发性麻醉药, 缺氧/复氧, 心肌保护, 三磷酸腺苷(ATP)

Abstract: Aim To study the effects of preconditioning with desflurane, sevoflurane and isoflurane on adenosine triphosphate (A TP)in anoxia-reoxygenation myocardial cells.Methods Rat ventricular myocytes, cultured for 4 ~ 5 days, were randomly allocated to five groups:Control group, anoxia-reoxygenation group and groups preconditioned with 1.5 MAC desflurane,sevoflurane or isoflurane follow inganoxia-reoxy genation.The content of intracellular ATP,the activities of lactic dehydrogenase(LDH)and creatine kinase(CK), and the cell viability were measured at the end of experiment.Results Preconditioning with 1.5 MAC desfllurane, sevoflurane or isoflurane significant lyattenuated the great reduction in ATP and cell viability and the increase of LDH and CK caused by anoxia-reoxygenation.There was a positive correlation ship between A TP and cell viability, and anegatiue correlation ship between LDH and CK (r was 0.83, -0.87 and -0.82 respectively, P<0.01).Conclusion sPreconditioning with desflurane, sevoflurane or isoflurane increases the preservation of ATP in anoxia-reoxygenation myocardial cells, which may be one of the mechanisms for myocardial protection.

Key words: volatile anesthetics, anoxia-reoxygenation, myocardial protection, adenosine triphosphate

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