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心房ATP敏感性钾通道的机械敏感性门控

Mechanosensitive gating of atrial ATP-sensitive potassium channels.

作者信息

Van Wagoner D R

机构信息

Department of Cardiovascular Biology, Cleveland Clinic Foundation, Ohio 44195-5069.

出版信息

Circ Res. 1993 May;72(5):973-83. doi: 10.1161/01.res.72.5.973.

DOI:10.1161/01.res.72.5.973
PMID:8477531
Abstract

Cell-attached and inside-out excised-patch recording techniques were used to search for mechanosensitive ion channels in neonatal and adult rat atrial myocytes. A channel activated by negative pressure applied to the patch, with a single-channel conductance of 52 pS in symmetric potassium solutions, was frequently observed. This channel has been identified as the atrial ATP-sensitive potassium (KATP) channel on the basis of its potassium selectivity, as well as its inhibition by ATP or tolbutamide in the inside-out excised patch. Mechanosensitive modulation of the KATP channel has not previously been reported. In the presence of 1 mM ATP, 10-50 microM pinacidil (a specific KATP channel agonist) does not significantly increase basal KATP channel activity; however, these concentrations of pinacidil potentiated the mechanosensitive modulation of the KATP channel. A hypotonic swelling protocol (a mechanical stimulus) was used in an effort to determine whether mechanosensitive modulation of this channel can generate significant whole-cell currents. Under perforated-patch whole-cell recording conditions, superfusion of atrial myocytes with a 240 mosm/kg solution (control solution, 290 mosm/kg) stimulated whole-cell currents with a magnitude similar to those activated by 10 microM pinacidil. These results demonstrate that the gating of the atrial KATP channel is mechanosensitive and suggest that mechanosensitive modulation may be an additional and significant mechanism, modulating channel activity under both physiological and pathological conditions.

摘要

采用细胞贴附式和内向外膜片钳记录技术,在新生和成年大鼠心房肌细胞中寻找机械敏感性离子通道。经常观察到一种通道,该通道在膜片上施加负压时被激活,在对称钾溶液中其单通道电导为52 pS。根据其钾选择性以及在内向外膜片钳中被ATP或甲苯磺丁脲抑制的特性,该通道已被鉴定为心房ATP敏感性钾(KATP)通道。此前尚未报道过KATP通道的机械敏感性调节。在存在1 mM ATP的情况下,10 - 50 microM吡那地尔(一种特异性KATP通道激动剂)不会显著增加基础KATP通道活性;然而,这些浓度的吡那地尔增强了KATP通道的机械敏感性调节。使用低渗肿胀方案(一种机械刺激)来确定该通道的机械敏感性调节是否能产生显著的全细胞电流。在穿孔膜片全细胞记录条件下,用240 mosm/kg溶液(对照溶液为290 mosm/kg)灌注心房肌细胞,刺激产生的全细胞电流大小与10 microM吡那地尔激活的电流相似。这些结果表明,心房KATP通道的门控具有机械敏感性,并提示机械敏感性调节可能是一种额外且重要的机制,在生理和病理条件下调节通道活性。

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