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钾离子ATP通道激动剂比马卡林对低温诱导的豚鼠离体心室肌动作电位延长的逆转作用

Reversal of hypothermia-induced action potential lengthening by the KATP channel agonist bimakalim in isolated guinea pig ventricular muscle.

作者信息

Lathrop D A, Contney S J, Bosnjak Z J, Stowe D F

机构信息

Department of Anesthesiology, Medical College of Wisconsin, Milwaukee 53226, USA.

出版信息

Gen Pharmacol. 1998 Jul;31(1):125-31. doi: 10.1016/s0306-3623(97)00395-9.

Abstract
  1. ATP-sensitive potassium (KATP) channel openers shorten cardiac ventricular muscle action potential duration (APD), reduce resting and developed contractile force, and have been shown to provide cardioprotection when given before, during, and after either short-term ischemia or long-term hypothermia. The authors' aim was to determine the concentration-dependent effect of the potent KATP channel opener bimakalim on transmembrane action potential changes induced by mild (27 degrees C) and moderate (20 degrees C) hypothermia in isolated guinea pig ventricular muscle. 2. Conventional microelectrode techniques were used to record action potentials (APs) in single myocytes during normothermia (37 degrees C) and hypothermia in the presence and absence of 0.1 to 30 mumol.l-1 bimakalim. 3. Hypothermia alone increased APD and depolarized the diastolic membrane potential (DMP): APD90 = 141.7 +/- 7.0 msec and DMP -86.2 +/- 1.4 mV (n = 6) at 37 degrees C versus 235.7 +/- 7.8 msec and -75.6 +/- 1.0 mV at 20 degrees C (n = 7). At 37 degrees C, bimakalim (0.1-10 mumol.l-1) shortened APD in a concentration-dependent fashion. 4. APD90 was markedly reduced from 141.7 +/- 7.0 msec without bimakalim to 9.5 +/- 2.6 msec with 10 mumol.l-1 bimakalim (n = 6); this effect was blocked by glibenclamide. DMP was hyperpolarized by bimakalim. More bimakalim was required to shorten APs during mild and moderate hypothermia. The 50% effective concentration (EC50) of bimakalim required to maximally shorten APD90 was 0.96 +/- 0.10 mumol.l-1 at 37 degrees C; this increased to 3.96 +/- 0.24 mumol.l-1 at 27 degrees C, and to 12.34 +/- 0.72 mumol.l-1 at 20 degrees C. Relative to hypothermia-induced depolarization, bimakalim hyperpolarized DMP toward drug-free values obtained at 37 degrees C. 5. These results indicate that hypothermia shifts the bimakalim concentration APD90 response curve to the right such that 13 times more bimakalim is required at 20 degrees C shorten APD by the same amount as at 37 degrees C. Bimakalim also reverses hypothermia-induced AP lengthening and tends to reverse the hypothermia-induced decrease in DMP. 6. These findings aid in our understanding of the cardioprotective effects of KATP channel openers during hypothermia.
摘要
  1. ATP敏感性钾(KATP)通道开放剂可缩短心室肌动作电位时程(APD),降低静息收缩力和最大收缩力,并且已证实,在短期缺血或长期低温之前、期间及之后给予该药物,可起到心脏保护作用。作者的目的是确定强效KATP通道开放剂苄甲卡利对豚鼠离体心室肌在轻度(27℃)和中度(20℃)低温时诱导的跨膜动作电位变化的浓度依赖性影响。2. 采用传统微电极技术记录正常体温(37℃)以及存在和不存在0.1至30μmol·l-1苄甲卡利时低温状态下单个心肌细胞的动作电位(AP)。3. 单纯低温可延长APD并使舒张期膜电位(DMP)去极化:37℃时APD90 = 141.7±7.0毫秒,DMP为-86.2±1.4毫伏(n = 6),而20℃时分别为235.7±7.8毫秒和-75.6±1.0毫伏(n = 7)。在37℃时,苄甲卡利(0.1 - 10μmol·l-1)以浓度依赖性方式缩短APD。4. APD90在无苄甲卡利时为141.7±7.0毫秒,在有10μmol·l-1苄甲卡利时显著降至9.5±2.6毫秒(n = 6);该效应被格列本脲阻断。苄甲卡利使DMP超极化。在轻度和中度低温时需要更多的苄甲卡利来缩短AP。最大程度缩短APD90所需的苄甲卡利50%有效浓度(EC50)在37℃时为0.96±0.10μmol·l-1;在27℃时增至3.9 .6±0.24μmol·l-1,在20℃时为12.34±0.72μmol·l-1。相对于低温诱导的去极化,苄甲卡利使DMP超极化至37℃时无药物作用的值。5. 这些结果表明,低温使苄甲卡利浓度-APD90反应曲线右移,以至于在20℃时需要13倍以上的苄甲卡利才能像在37℃时一样缩短相同幅度的APD。苄甲卡利还可逆转低温诱导的AP延长,并倾向于逆转低温诱导的DMP降低。6. 这些发现有助于我们理解低温期间KATP通道开放剂的心脏保护作用。

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