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青蛙胃底的氯离子转运:奥美拉唑的作用

Chloride transport of frog gastric fundus: effects of omeprazole.

作者信息

Starlinger M J, Hollands M J, Rowe P H, Matthews J B, Silen W

出版信息

Am J Physiol. 1986 Jan;250(1 Pt 1):G118-26. doi: 10.1152/ajpgi.1986.250.1.G118.

Abstract

Omeprazole (10(-4) M) inhibited H+ secretion and increased potential difference (PD), resistance, and short-circuit current (Isc) in chambered bullfrog gastric mucosa, but the electrical changes developed only in tissues previously exposed to histamine. Net chloride transport (JnetCl) did not change after omeprazole under short-circuited conditions, and Isc increased to become equal to JnetCl. Under open-circuit conditions, JnetCl was reduced by 38%, the decrement attributable to the concomitant increase in PD, as evidenced by a linear relationship between JnetCl and PD in omeprazole-treated mucosae clamped to different PD (0-45 mV). The effect of omeprazole on PD and Isc could be blocked by metiamide and was absent in spontaneously resting tissues. HEPES nutrient solutions did not alter the electrical response or Cl- transport after omeprazole. In Na+-free solutions, omeprazole induced only a transient rise in PD and Isc. We conclude that omeprazole uncouples H+ and Cl- secretion. This Cl- secretion is electrogenic and dependent upon stimulation by histamine. Both Na+ and HCO3- seem to be involved in movement of Cl- across the basolateral membrane.

摘要

奥美拉唑(10⁻⁴ M)抑制牛蛙带腔胃黏膜中的H⁺分泌,并增加电位差(PD)、电阻和短路电流(Isc),但电变化仅在先前暴露于组胺的组织中出现。在短路条件下,奥美拉唑作用后净氯转运(JnetCl)未发生变化,且Isc增加至与JnetCl相等。在开路条件下,JnetCl降低了38%,该减少归因于PD的同时增加,这在钳制于不同PD(0 - 45 mV)的经奥美拉唑处理的黏膜中JnetCl与PD之间的线性关系中得到证明。奥美拉唑对PD和Isc的作用可被甲硫咪特阻断,且在自发静息的组织中不存在该作用。在奥美拉唑作用后,HEPES营养液未改变电反应或Cl⁻转运。在无Na⁺溶液中,奥美拉唑仅诱导PD和Isc出现短暂升高。我们得出结论,奥美拉唑使H⁺和Cl⁻分泌解偶联。这种Cl⁻分泌是生电性的,且依赖于组胺的刺激。Na⁺和HCO₃⁻似乎都参与Cl⁻跨基底外侧膜的转运。

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