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毒毛花苷对离体胃黏膜分泌的抑制作用。

The inhibitory effect of strophanthidin on secretion by the isolated gastric mucosa.

作者信息

COOPERSTEIN I L

出版信息

J Gen Physiol. 1959 Jul 20;42(6):1233-9. doi: 10.1085/jgp.42.6.1233.

Abstract

The unidirectional fluxes of Na(+) and Cl(-) were measured across the isolated gastric mucosa of the bullfrog (R. catesbiana). The addition of strophanthidin, a cardiac aglycone, resulted in marked reductions of the spontaneous potential and short-circuit current. Associated with these changes, the isolated gastric mucosa ceased secreting chloride and hydrogen ion. Although the active component of chloride transfer was inhibited, the exchange diffusion component seemed to increase. No significant changes in membrane conductance or sodium flux were noted. Possible mechanisms of strophanthidin inhibition were discussed in view of its effect on chloride transport across the gastric mucosa and on sodium and potassium transfer in other tissues. It was concluded that the cardiac glycosides may not be specific inhibitors of sodium and potassium transport. This non-specific inhibition suggests that active chloride transport is affected by strophanthidin directly and/or anion secretion is dependent upon normal functioning of cation transport systems in the tissue.

摘要

测量了牛蛙(R. catesbiana)离体胃黏膜上Na(+)和Cl(-)的单向通量。加入毒毛花苷元(一种强心苷配基)后,自发电位和短路电流显著降低。伴随着这些变化,离体胃黏膜停止分泌氯离子和氢离子。虽然氯离子转运的主动成分受到抑制,但交换扩散成分似乎增加。未观察到膜电导或钠通量有显著变化。鉴于毒毛花苷元对氯离子跨胃黏膜转运以及对其他组织中钠和钾转运的影响,讨论了其抑制作用的可能机制。得出的结论是,强心苷可能不是钠和钾转运的特异性抑制剂。这种非特异性抑制表明,毒毛花苷元直接影响氯离子的主动转运,和/或阴离子分泌依赖于组织中阳离子转运系统的正常功能。

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