Vanheel B, de Hemptinne A
Laboratory of Normal and Pathological Physiology, University of Gent, Belgium.
Cardiovasc Res. 1992 Nov;26(11):1030-9. doi: 10.1093/cvr/26.11.1030.
The aim was to investigate the effect of pre-exposure to inhibitors or activators of the ATP regulated K+ (KATP) channels on the ischaemia induced early changes of the extracellular K+ concentration, the extracellular pH, and the action potential in mammalian cardiac tissue.
An in vitro model simulating ischaemia was applied to isolated guinea pig papillary muscles while simultaneous microelectrode measurements of the transmembrane potentials and of the pH and K+ activity at the surface of the preparation (pHs and asK respectively) were made.
During conditions of superfusion arrest, when accumulation of metabolic acids causes acidification of pHs, the simultaneous development of a true hypoxic state of the muscle is required in order to induce shortening of the action potential duration and accumulation of extracellular K+ with associated membrane depolarisation. Glibenclamide (10-50 microM) slowed the decrease of the action potential duration in 50% of the muscles, while the increase of asK was only moderately (approximately 20%) influenced. In the presence of 200 microM of the KATP channel inhibitor, the mean K+ accumulation was not significantly different from the control. The presence of tolbutamide (1 mM) had no effect on the decrease of action potential duration, but moderately slowed the increase of asK. Superfusion with lemakalim (BRL 38227) decreased action potential duration dose dependently. In papillary muscles in which action potential duration was shortened to approximately 60% of the control duration by presuperfusion with lemakalim, a subsequent ischaemic episode did not increase but rather delayed the rise in asK. During simulated ischaemia in the presence of Ba2+ ions (1 mM), asK showed a transient decrease followed by a rise at a rate similar to that in the absence of Ba2+.
Early ischaemic K+ accumulation and surface acidification are relatively insensitive to KATP channel inhibition or activation prior to the ischaemic insult. The rather loose coupling of the increase of asK and the decrease of action potential duration, as well as the limited effect of sulphonylureas on the K+ increase, suggests that mechanisms other than KATP channel opening could possibly contribute to the initial phase of ischaemic K+ accumulation.
研究预先暴露于ATP调节钾离子(KATP)通道抑制剂或激活剂对哺乳动物心脏组织缺血诱导的细胞外钾离子浓度、细胞外pH值及动作电位早期变化的影响。
将模拟缺血的体外模型应用于分离的豚鼠乳头肌,同时用微电极测量跨膜电位以及标本表面的pH值和钾离子活性(分别为pHs和asK)。
在灌流停止的情况下,当代谢性酸的积累导致pHs酸化时,为了诱导动作电位时程缩短以及细胞外钾离子积累并伴有膜去极化,肌肉需要同时出现真正的缺氧状态。格列本脲(10 - 50微摩尔)使50%的肌肉中动作电位时程的缩短减慢,而asK的增加仅受到中度(约20%)影响。在存在200微摩尔KATP通道抑制剂的情况下,平均钾离子积累与对照组无显著差异。甲苯磺丁脲(1毫摩尔)的存在对动作电位时程的缩短无影响,但中度减慢了asK的增加。用雷马卡林(BRL 38227)灌流剂量依赖性地缩短动作电位时程。在预先用雷马卡林灌流使动作电位时程缩短至对照时程约60%的乳头肌中,随后的缺血发作并未使asK升高,反而延迟了其升高。在存在钡离子(1毫摩尔)的情况下进行模拟缺血时,asK先出现短暂下降,随后以与无钡离子时相似的速率上升。
在缺血损伤之前,早期缺血性钾离子积累和表面酸化对KATP通道抑制或激活相对不敏感。asK增加与动作电位时程缩短之间的耦合较为松散,以及磺脲类药物对钾离子增加的有限作用表明,除KATP通道开放外的其他机制可能参与了缺血性钾离子积累的初始阶段。