Jaswinder S. Gill, William J. McKenna, A.John Camm
{"title":"自由基不可逆地降低离体豚鼠心室肌细胞的Ca2+电流","authors":"Jaswinder S. Gill, William J. McKenna, A.John Camm","doi":"10.1016/0926-6917(95)90042-X","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of free radicals on voltage-gates Ca<sup>2+</sup> currents (<em>I</em><sub>Ca</sub>) were investigated in single guinea-pig ventricular myocytes using the whole-cell clamp technique. <em>I</em><sub>Ca</sub> 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. <em>I</em><sub>Ca</sub> decreased from 846 ± 533 (S.D.) pA to 688 ± 444 pA (<em>n</em> = 7, <em>P</em> < 0.05) in the presence of 100 μM cumene hydroperoxide and from 708 ± 157 pA to 457 ± 163 pA(<em>n</em> = 5, <em>P</em> < 0.0001) in the presence of 500 μM cumene hydroperoxide. <em>I</em><sub>Ca</sub> 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 <em>I</em><sub>Ca</sub> could not be restored by washing for up to 5 min using normal recording solution. We conclude that <em>I</em><sub>Ca</sub> is decreased in the presence of cumene hydroperoxide and an oxygen-derived free radical generating system in single guinea-pig ventricular myocytes. The cellular Ca<sup>2+</sup> overload observed in free radical mediated reperfusion injury is therefore unlikely to result from an increase in sacrolemmal Ca<sup>2+</sup> entry via voltage-gated Ca<sup>2+</sup> channels.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"292 3","pages":"Pages 337-340"},"PeriodicalIF":0.0000,"publicationDate":"1995-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)90042-X","citationCount":"57","resultStr":"{\"title\":\"Free radicals irreversibly decrease Ca2+ currents in isolated guinea-pig ventricular myocytes\",\"authors\":\"Jaswinder S. Gill, William J. McKenna, A.John Camm\",\"doi\":\"10.1016/0926-6917(95)90042-X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The effects of free radicals on voltage-gates Ca<sup>2+</sup> currents (<em>I</em><sub>Ca</sub>) were investigated in single guinea-pig ventricular myocytes using the whole-cell clamp technique. <em>I</em><sub>Ca</sub> 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. <em>I</em><sub>Ca</sub> decreased from 846 ± 533 (S.D.) pA to 688 ± 444 pA (<em>n</em> = 7, <em>P</em> < 0.05) in the presence of 100 μM cumene hydroperoxide and from 708 ± 157 pA to 457 ± 163 pA(<em>n</em> = 5, <em>P</em> < 0.0001) in the presence of 500 μM cumene hydroperoxide. <em>I</em><sub>Ca</sub> 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 <em>I</em><sub>Ca</sub> could not be restored by washing for up to 5 min using normal recording solution. We conclude that <em>I</em><sub>Ca</sub> is decreased in the presence of cumene hydroperoxide and an oxygen-derived free radical generating system in single guinea-pig ventricular myocytes. The cellular Ca<sup>2+</sup> overload observed in free radical mediated reperfusion injury is therefore unlikely to result from an increase in sacrolemmal Ca<sup>2+</sup> entry via voltage-gated Ca<sup>2+</sup> channels.</p></div>\",\"PeriodicalId\":100501,\"journal\":{\"name\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"volume\":\"292 3\",\"pages\":\"Pages 337-340\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-03-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6917(95)90042-X\",\"citationCount\":\"57\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/092669179590042X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/092669179590042X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 57
摘要
利用全细胞箝位技术研究了自由基对豚鼠心室肌细胞电压门Ca2+电流(ICa)的影响。ICa是在基线状态下测量的,在使用过氧化氢异丙苯自由基或在黄嘌呤氧化酶中加入嘌呤产生自由基后测量的。ICa由846±533 (sd) pA降至688±444 pA (n = 7, P <0.05),从708±157 pA到457±163 pA(n = 5, P <0.0001), 500 μM的异丙烯过氧化氢存在。在自由基生成系统(2.3 mM嘌呤+ 20 U/l黄嘌呤氧化酶)的作用下,ICa从1303±560 pA降至965±360 pA。还原的ICa不能通过使用正常的记录溶液洗涤长达5分钟来恢复。我们得出结论,在单豚鼠心室肌细胞中,在过氧化氢异丙苯和氧源自由基生成系统的存在下,ICa减少。因此,在自由基介导的再灌注损伤中观察到的细胞Ca2+过载不太可能是由于通过电压门控Ca2+通道的骶管Ca2+进入增加引起的。
The effects of free radicals on voltage-gates 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 μM cumene hydroperoxide and from 708 ± 157 pA to 457 ± 163 pA(n = 5, P < 0.0001) in the presence of 500 μM 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 sacrolemmal Ca2+ entry via voltage-gated Ca2+ channels.