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过氧化氢、乙二醇双乙醚二胺四乙酸(EGTA)与猫心室肌细胞膜片钳记录方法之间的相互作用

Interactions of H2O2, EGTA and patch pipette recording methods in feline ventricular myocytes.

作者信息

Barrington P L

机构信息

Department of Pharmacology, Northwestern University, Chicago, IL 60611.

出版信息

J Mol Cell Cardiol. 1994 May;26(5):557-68. doi: 10.1006/jmcc.1994.1068.

Abstract

Free radical generating systems produce a sequence of changes in the action potentials of isolated cardiac myocytes. Efforts to understand the nature of the alterations in ionic currents have yielded mixed results. The use of patch-pipettes for voltage-clamp experiments and manipulation of pipette solution composition may contribute to the confusion. In this study, action potentials were recorded from feline ventricular myocytes during exposure to 100 microM H2O2. Action potential changes recorded with conventional, high resistance microelectrodes occurred in three stages as previously reported. The action potential changes recorded with patch-pipettes showed increases in action potential duration, notch and plateau potentials over time. These cells did not display after depolarizations or loss of excitability as seen with conventional microelectrodes. With the patch-pipette method, untreated control cells had time-dependent changes in the action potentials. When the pipette filling solution was modified by the addition of 5 mM EGTA, the H2O2-induced changes appeared reduced but not eliminated. The initial control values of action potential parameters before exposure to H2O2 varied with the presence or absence of EGTA. These data show both direct effects of EGTA and of time on action potential parameters independent of H2O2-exposure. These artifacts of the patch-pipette method and the composition of the pipette solutions affect the sequence of changes in the action potential during exposure to H2O2.

摘要

自由基生成系统会使分离的心肌细胞动作电位发生一系列变化。为了解离子电流变化本质所做的努力得到了不一致的结果。在电压钳实验中使用膜片吸管以及对吸管溶液成分的操控可能导致了这种混淆。在本研究中,在暴露于100微摩尔过氧化氢期间记录了猫心室肌细胞的动作电位。如先前报道的那样,用传统的高电阻微电极记录的动作电位变化分三个阶段出现。用膜片吸管记录的动作电位变化显示,动作电位持续时间、切迹和平台电位随时间增加。这些细胞没有表现出传统微电极所见的去极化后电位或兴奋性丧失。使用膜片吸管方法时,未处理的对照细胞的动作电位有时间依赖性变化。当通过添加5毫摩尔乙二醇双乙胺醚来改变吸管填充溶液时,过氧化氢诱导的变化似乎减少但并未消除。暴露于过氧化氢之前动作电位参数的初始对照值因有无乙二醇双乙胺醚而有所不同。这些数据表明乙二醇双乙胺醚和时间对动作电位参数都有独立于过氧化氢暴露的直接影响。膜片吸管方法的这些假象以及吸管溶液的成分会影响暴露于过氧化氢期间动作电位的变化顺序。

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