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视网膜电图钾离子通道调节胆囊平滑肌的电活动和收缩活动。

ERG K+ channels modulate the electrical and contractile activities of gallbladder smooth muscle.

作者信息

Parr Edward, Pozo Maria J, Horowitz Burton, Nelson Mark T, Mawe Gary M

机构信息

Department of Anatomy and Neurobiology, The University of Vermont, Burlington, VT 05405, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2003 Mar;284(3):G392-8. doi: 10.1152/ajpgi.00325.2002. Epub 2002 Nov 13.

Abstract

The current study was undertaken to test the existence and possible role of ether-a-go-go-related gene 1 (ERG1) protein K(+) channels in gallbladder smooth muscle (GBSM). Transcripts encoding ERG1 were detected in human, mouse, and guinea pig GBSM, and ERG1 immunoreactivity was observed in GBSM cells. In intracellular voltage recordings, addition of E-4031 (100 nM-1 microM) or cisapride (100 nM-2 microM) caused concentration-dependent excitation of guinea pig GBSM that was not affected by 500 nM TTX + 5 microM atropine, and E-4031 also depolarized the resting membrane potential. In muscle strip studies, E-4031 either induced phasic contractions or significantly increased the amplitude of phasic contractions in spontaneously active tissues (P = 0.001). E-4031 also potentiated bethanechol-induced contractions. In conclusion, ERG1 channels are expressed in the GBSM, where they play a role in excitation-contraction coupling probably by contributing to repolarization of the plateau phase of the action potential and to the resting membrane potential.

摘要

本研究旨在检测醚 - 去极化相关基因1(ERG1)蛋白钾通道在胆囊平滑肌(GBSM)中的存在及其可能的作用。在人、小鼠和豚鼠的GBSM中检测到编码ERG1的转录本,并在GBSM细胞中观察到ERG1免疫反应性。在细胞内电压记录中,加入E - 4031(100 nM - 1 μM)或西沙必利(100 nM - 2 μM)会引起豚鼠GBSM浓度依赖性兴奋,500 nM 河豚毒素 + 5 μM 阿托品对此无影响,且E - 4031还使静息膜电位去极化。在肌条研究中,E - 4031在自发活动组织中要么诱导相性收缩,要么显著增加相性收缩的幅度(P = 0.001)。E - 4031还增强了氨甲酰甲胆碱诱导的收缩。总之,ERG1通道在GBSM中表达,它们可能通过促进动作电位平台期的复极化和静息膜电位在兴奋 - 收缩偶联中发挥作用。

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