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作 者:赵美眯[1] 连雯雯[1] 孙睿[1] 王红梅[1] 封瑞[1] 胡慧媛[1] 孙雪菲[1] 郝丽英[1]
机构地区:[1]中国医科大学药学院药物毒理教研室,沈阳110001
出 处:《生理学报》2014年第6期718-722,共5页Acta Physiologica Sinica
基 金:supported by the National Natural Science Foundation of China(No.31071004)
摘 要:本文旨在研究细胞内高镁对离体豚鼠心室肌细胞L-型钙通道的单通道门控特性的影响。急性酶消化法分离豚鼠心室肌细胞,应用膜片钳膜内向外单通道记录模式观察不同浓度细胞内镁([Mg2+]i)对心肌细胞L-型钙通道单通道电流的影响。结果显示,对照组([Mg2+]i 0.9 mmol/L)的心肌细胞L-型钙通道相对活性为(176.5±34.1)%,而高镁组([Mg2+]i 8.1 mmol/L)钙通道相对活性显著降低至(64.8±18.1)%(P<0.05)。另外,8.1 mmol/L[Mg2+]i使心肌细胞L-型钙通道的平均开放时间缩短至对照组的约25%(P<0.05),但对通道平均关闭时间无明显影响。以上结果提示,细胞内高镁主要通过缩短通道平均开放时间抑制豚鼠心室肌细胞L-型钙通道的活性。This study is aimed to investigate the effects of high intracellular Mg2+ on L-type calcium channel in guinea-pig ventricular myocytes. The cardiomyocytes were acutely isolated with enzyme digestion method. By adopting inside-out configuration of patch clamp technique, single channel currents of the L-type calcium channel were recorded under different intracellular Mg2+ concentrations([Mg2+]i). In control group, which was treated with 0.9 mmol/L Mg2+, the relative activity of calcium channel was(176.5 ± 34.1)%(n = 7). When [Mg2+]i was increased from 0.9 to 8.1 mmol/L(high Mg2+ group), the relative activities of calcium channel decreased to(64.8 ± 18.1)%(n = 6, P 〈 0.05). Moreover, under 8.1 mmol/L Mg2+, the mean open time of calcium channel was shortened to about 25% of that under control condition(P 〈 0.05), but the mean close time of calcium channel was not altered. These results suggest that high intracellular Mg2+ may inhibit the activities of L-type calcium channel, which is mainly due to the shortening of the mean open time of single L-type calcium channel.
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