Suppr超能文献

牛蛙心房细胞中的两种ATP激活电导。

Two ATP-activated conductances in bullfrog atrial cells.

作者信息

Friel D D, Bean B P

机构信息

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Gen Physiol. 1988 Jan;91(1):1-27. doi: 10.1085/jgp.91.1.1.

Abstract

Currents activated by extracellular ATP were studied in single voltage-clamped bullfrog atrial cells. Rapid application of ATP elicited currents carried through two different conductance pathways: a rapidly desensitizing conductance reversing near -10 mV, and a maintained, inwardly rectifying conductance reversing near -85 mV. ATP activated the desensitizing component of current with a K 1/2 of approximately 50 microM and the maintained component with a K 1/2 of approximately 10 microM. Both types of current were activated by ATP but not by adenosine, AMP, or ADP. The desensitizing current was selectively inhibited by alpha, beta-methylene ATP, and the maintained, inwardly rectifying current was selectively suppressed by extracellular Cs. The desensitizing component of current was greatly reduced when extracellular Na was replaced by N-methylglucamine, but was slightly augmented when Na was replaced by Cs. GTP, ITP, and UTP were all ineffective in activating the desensitizing current, and of a variety of ATP analogues, only ATP-gamma-S was effective. Addition of EGTA or BAPTA to the intracellular solution did not obviously affect the desensitizing current. Fluctuation analysis of currents through the desensitizing conductance suggested that current is carried through ionic channels with a small (less than pS) unitary conductance.

摘要

在单个电压钳制的牛蛙心房细胞中研究了细胞外ATP激活的电流。快速施加ATP可引发通过两种不同电导途径传导的电流:一种是在-10 mV附近快速脱敏的电导,另一种是在-85 mV附近持续的内向整流电导。ATP以约50 microM的K 1/2激活电流的脱敏成分,以约10 microM的K 1/2激活持续成分。两种类型的电流均由ATP激活,而不由腺苷、AMP或ADP激活。脱敏电流被α,β-亚甲基ATP选择性抑制,持续的内向整流电流被细胞外Cs选择性抑制。当细胞外Na被N-甲基葡糖胺取代时,电流的脱敏成分大大降低,但当Na被Cs取代时略有增加。GTP、ITP和UTP均不能有效激活脱敏电流,在多种ATP类似物中,只有ATP-γ-S有效。向细胞内溶液中添加EGTA或BAPTA对脱敏电流没有明显影响。通过脱敏电导的电流波动分析表明,电流通过具有小(小于pS)单位电导的离子通道传导。

相似文献

4
An ATP-activated nonselective cation channel in guinea pig ventricular myocytes.
Am J Physiol. 1995 Sep;269(3 Pt 2):H789-97. doi: 10.1152/ajpheart.1995.269.3.H789.
6
Different properties of the atrial G protein-gated K+ channels activated by extracellular ATP and adenosine.
Am J Physiol. 1995 Oct;269(4 Pt 2):H1349-58. doi: 10.1152/ajpheart.1995.269.4.H1349.

引用本文的文献

3
Activation and regulation of purinergic P2X receptor channels.嘌呤能 P2X 受体通道的激活和调节。
Pharmacol Rev. 2011 Sep;63(3):641-83. doi: 10.1124/pr.110.003129. Epub 2011 Jul 7.
7
Inactivation of P2X2 purinoceptors by divalent cations.二价阳离子使P2X2嘌呤受体失活。
J Physiol. 2000 Jan 15;522 Pt 2(Pt 2):199-214. doi: 10.1111/j.1469-7793.2000.t01-1-00199.x.

本文引用的文献

9
The effect of adenyl compounds on the rat heart.腺苷化合物对大鼠心脏的影响。
Br J Pharmacol. 1983 May;79(1):211-8. doi: 10.1111/j.1476-5381.1983.tb10514.x.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验