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壁细胞分泌膜中氯离子传导的证据。

Evidence for a chloride conductance in secretory membrane of parietal cells.

作者信息

Perez A, Blissard D, Sachs G, Hersey S J

机构信息

Department of Physiology, Emory University, Atlanta, Georgia 30322.

出版信息

Am J Physiol. 1989 Feb;256(2 Pt 1):G299-305. doi: 10.1152/ajpgi.1989.256.2.G299.

Abstract

A fluorescence-quench method using acridine orange as the probe was employed to monitor acid formation in situ by detergent-permeabilized gastric glands. In KCl medium, the addition of ATP to the permeabilized glands resulted in a rapid decrease in fluorescence and addition of valinomycin resulted in a second phase of fluorescence quench. The fluorescence was restored by addition of the H+-K+-ATPase inhibitor, Sch 28080. An ATP-dependent fluorescence quench was observed also in K2SO4 or K+-isethionate medium; however, valinomycin was ineffective in the Cl-free media. The ATP-dependent quench could be reversed or prevented by the electrogenic protonophore, tetrachlorosalicylanilide (TCS), in KCl medium but not in Cl-free media. The results with TCS are interpreted as demonstrating a large Cl- conductance in the secretory membrane, whereas the results with valinomycin indicate that resting membranes lack a K+ conductance. The data suggest that a complex KCl pathway that may demonstrate a Cl- conductance is used to activate acid secretion.

摘要

采用以吖啶橙为探针的荧光猝灭法,原位监测去污剂通透处理的胃腺中酸的形成。在氯化钾培养基中,向通透处理的腺体中添加三磷酸腺苷(ATP)会导致荧光迅速降低,而添加缬氨霉素会导致荧光猝灭的第二阶段。添加H⁺-K⁺-ATP酶抑制剂Sch 28080后荧光恢复。在硫酸钾或异硫氰酸钾培养基中也观察到了依赖ATP的荧光猝灭;然而,缬氨霉素在无氯培养基中无效。在氯化钾培养基中,依赖ATP的猝灭可被产电质子载体四氯水杨酰苯胺(TCS)逆转或阻止,但在无氯培养基中则不行。TCS的结果被解释为表明分泌膜具有较大的氯离子电导,而缬氨霉素的结果表明静息膜缺乏钾离子电导。数据表明,一条可能显示氯离子电导的复杂氯化钾途径被用于激活酸分泌。

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