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3',5'-环磷酸腺苷刺激A6上皮细胞中的氯离子分泌。

Adenosine 3',5'-cyclic monophosphate stimulates chloride secretion in A6 epithelia.

作者信息

Yanase M, Handler J S

出版信息

Am J Physiol. 1986 Nov;251(5 Pt 1):C810-4. doi: 10.1152/ajpcell.1986.251.5.C810.

Abstract

Basal and aldosterone-stimulated short-circuit current (Isc) of A6 epithelia are known to be equivalent to net apical to basal Na flux and are completely inhibited by 0.05 mM amiloride added to the solution bathing the apical surface of the epithelium. In the absence of amiloride, the Isc stimulated by adenosine 3',5'-cyclic monophosphate (cAMP) is also equivalent to net apical to basal Na flux. However, amiloride does not completely inhibit the cAMP-stimulated Isc. In this study, the cAMP-stimulated, amiloride-insensitive Isc was characterized, using vasopressin or forskolin to raise cell cAMP. After basal Isc is inhibited by amiloride, forskolin stimulates Isc, conductance, and bidirectional 36Cl flux. Stimulation of Isc depends on the presence of both Na and Cl; stimulation of conductance depends on the presence of Cl. 36Cl flux studies showed that the cAMP-stimulated, amiloride-insensitive Isc is equivalent to net Cl flux. It is inhibited by ouabain and by furosemide or bumetanide added to the solution bathing the basal surface of the epithelium. In view of the effect of cAMP in some other epithelia, we suggest that cAMP activates apical membrane Cl channels that are in series with a Na-K-Cl cotransporter in the basolateral plasma membrane.

摘要

已知A6上皮细胞的基础短路电流(Isc)和醛固酮刺激的短路电流等同于从顶端到基底的净钠通量,并且当向浸泡上皮细胞顶端表面的溶液中添加0.05 mM氨氯吡脒时,该电流会被完全抑制。在没有氨氯吡脒的情况下,由3',5'-环磷酸腺苷(cAMP)刺激的Isc也等同于从顶端到基底的净钠通量。然而,氨氯吡脒并不能完全抑制cAMP刺激的Isc。在本研究中,利用血管加压素或福斯可林提高细胞内cAMP水平,对cAMP刺激的、氨氯吡脒不敏感的Isc进行了表征。在氨氯吡脒抑制基础Isc后,福斯可林刺激Isc、电导和双向36Cl通量。Isc的刺激依赖于Na和Cl的同时存在;电导的刺激依赖于Cl的存在。36Cl通量研究表明,cAMP刺激的、氨氯吡脒不敏感的Isc等同于净Cl通量。它会被哇巴因以及添加到浸泡上皮细胞基底表面溶液中的呋塞米或布美他尼所抑制。鉴于cAMP在其他一些上皮细胞中的作用,我们认为cAMP激活了顶端膜Cl通道,该通道与基底外侧质膜中的Na-K-Cl共转运体串联。

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