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钾离子通道和氯离子通道在负鼠下食管括约肌张力维持中的相反作用

Opposing roles of K(+) and Cl(-) channels in maintenance of opossum lower esophageal sphincter tone.

作者信息

Zhang Y, Miller D V, Paterson W G

机构信息

Gastrointestinal Diseases Research Unit and Departments of Medicine and Physiology, Queen's University, Kingston, Ontario, Canada K7L 5G2.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2000 Dec;279(6):G1226-34. doi: 10.1152/ajpgi.2000.279.6.G1226.

Abstract

The ionic basis underlying the maintenance of myogenic tone of lower esophageal sphincter circular muscle (LES) was investigated in opossum with the use of standard isometric tension and conventional intracellular microelectrode recordings in vitro. In tension recording studies, nifedipine (1 microM) reduced basal tone to 27.7 +/- 3.8% of control. The K(+) channel blockers tetraethylammonium (TEA, 2 mM), charybdotoxin (100 nM), and 4-aminopyridine (4-AP, 2 mM) enhanced resting tone, whereas apamin and glibenclamide were without affect. Cl(-) channel blockers DIDS (500 microM) and 5-nitro-2-(3-phenylpropylamino)-benzoic acid (500 microM), as well as niflumic acid (0.1-300 microM), decreased basal tone, but tamoxifen was without effect. Intracellular microelectrode recordings revealed ongoing, spontaneous, spike-like action potentials (APs). Nifedipine abolished APs and depolarized resting membrane potential (RMP). Both TEA and 4-AP significantly depolarized RMP and augmented APs, whereas niflumic acid dose-dependently hyperpolarized RMP and abolished APs. These data suggest that, in the opossum, basal tone is associated with continuous APs and that K(+) and Ca(2+)-activated Cl(-) channels have important opposing roles in the genesis of LES tone.

摘要

利用标准等长张力和传统细胞内微电极体外记录技术,在负鼠中研究了食管下括约肌环形肌(LES)肌源性张力维持的离子基础。在张力记录研究中,硝苯地平(1 microM)将基础张力降低至对照的27.7 +/- 3.8%。钾通道阻滞剂四乙铵(TEA,2 mM)、蝎毒素(100 nM)和4-氨基吡啶(4-AP,2 mM)增强静息张力,而蜂毒明肽和格列本脲则无影响。氯通道阻滞剂二异硫氰酸二苯乙烯酯(DIDS,500 microM)和5-硝基-2-(3-苯丙基氨基)-苯甲酸(500 microM)以及氟灭酸(0.1 - 三百 microM)降低基础张力,但他莫昔芬无作用。细胞内微电极记录显示存在持续的、自发的、尖峰样动作电位(APs)。硝苯地平消除APs并使静息膜电位(RMP)去极化。TEA和4-AP均显著使RMP去极化并增强APs,而氟灭酸剂量依赖性地使RMP超极化并消除APs。这些数据表明,在负鼠中,基础张力与持续的APs相关,并且钾通道和钙激活氯通道在LES张力的产生中具有重要的相反作用。

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