Gill J S, McKenna W J, Camm A J
Department of Cardiological Sciences, St George's Hospital Medical School, London, UK.
Eur J Pharmacol. 1995 Mar 16;292(3-4):337-40. doi: 10.1016/0926-6917(95)90042-x.
The effects of free radicals on voltage-gated Ca2+ currents (ICa) were investigated in single guinea-pig ventricular myocytes using the whole-cell clamp technique. ICa was measured in the baseline state and after the application of free radicals from cumene hydroperoxide or generated from the addition of purine to xanthine oxidase. ICa decreased from 846 +/- 533 (S.D.) pA to 688 +/- 444 pA (n = 7, P < 0.05) in the presence of 100 microM cumene hydroperoxide and from 708 +/- 157 pA to 457 +/- 163 pA (n = 5, P < 0.0001) in the presence of 500 microM cumene hydroperoxide. ICa also decreased from 1303 +/- 560 pA to 965 +/- 360 pA in the presence of the free radical generating system (2.3 mM purine plus 20 U/l xanthine oxidase). The reduced ICa could not be restored by washing for up to 5 min using normal recording solution. We conclude that ICa is decreased in the presence of cumene hydroperoxide and an oxygen-derived free radical generating system in single guinea-pig ventricular myocytes. The cellular Ca2+ overload observed in free radical mediated reperfusion injury is therefore unlikely to result from an increase in sarcolemmal Ca2+ entry via voltage-gated Ca2+ channels.
运用全细胞膜片钳技术,在豚鼠单个心室肌细胞中研究了自由基对电压门控性Ca2+电流(ICa)的影响。在基线状态以及加入异丙苯过氧化氢产生的自由基或加入嘌呤与黄嘌呤氧化酶生成的自由基后,测量ICa。在存在100微摩尔异丙苯过氧化氢时,ICa从846±533(标准差)皮安降至688±444皮安(n = 7,P < 0.05);在存在500微摩尔异丙苯过氧化氢时,ICa从708±157皮安降至457±163皮安(n = 5,P < 0.0001)。在自由基生成系统(2.3毫摩尔嘌呤加20单位/升黄嘌呤氧化酶)存在时,ICa也从1303±560皮安降至965±360皮安。使用正常记录溶液冲洗长达5分钟,无法恢复降低的ICa。我们得出结论,在豚鼠单个心室肌细胞中,存在异丙苯过氧化氢和氧衍生自由基生成系统时,ICa降低。因此,在自由基介导的再灌注损伤中观察到的细胞Ca2+超载不太可能是由于通过电压门控性Ca2+通道的肌膜Ca2+内流增加所致。