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环磷酸腺苷依赖性调节大鼠远端结肠中的钾离子转运

Cyclic AMP-dependent regulation of K+ transport in the rat distal colon.

作者信息

Diener M, Hug F, Strabel D, Scharrer E

机构信息

Institut für Veterinär-Physiologie, Universität Zürich, Switzerland.

出版信息

Br J Pharmacol. 1996 Jul;118(6):1477-87. doi: 10.1111/j.1476-5381.1996.tb15563.x.

Abstract
  1. The effect of agonists of the cyclic AMP pathway and of 293B, a chromanole-derived K+ channel blocker, on K+ transport in the rat distal colon was studied by measuring unidirectional fluxes, uptake, and efflux of Rb+ in mucosa-submucosa preparations and by patch-clamp of crypt epithelia from isolated crypts. 2. 293B concentration-dependently inhibited basal and forskolin-stimulated short-circuit current. In isolated crypts 293B blocked a basal K+ conductance but had no effect on cyclic AMP-evoked depolarization induced by the opening of apical Cl- channels. When the effect of cyclic AMP on Cl- conductance was prevented by substituting Cl- with gluconate, an inhibition of total cellular K+ conductance by forskolin and a membrane-permeable cyclic AMP analogue was unmasked. 3. Unidirectional ion flux measurements revealed that 293B suppressed the increase in JRbsm induced by forskolin. This, together with the inhibition of cyclic AMP-induced anion secretion indicates that the drug blocks K+ channels, presumably both in the apical and the basolateral membrane. Forskolin caused not only inhibition of K+ absorption, but also stimulation of K+ secretion. The inhibition was diminished, but not blocked, in the presence of inhibitors of the apical H(+)-K(+)-ATPase, vanadate and ouabain. Forskolin stimulated serosal, bumetanide-sensitive Rb+ uptake, whereas mucosal, ouabain/vanadate-sensitive uptake remained unaffected. 4. Efflux experiments revealed that forskolin caused a redistribution of cellular K+ efflux reducing the ratio of basolateral versus apical Rb+ efflux. 5. These results suggest that intracellular cyclic AMP exerts its effects on K+ transport by several mechanisms: an increase in the driving force for K+ efflux due to the depolarization induced by opening of Cl- channels, a stimulation of the basolateral uptake of K+ via the Na(+)-K(+)-Cl(-)-cotransporter, and a decrease of the ratio of basolateral versus apical K+ conductance leading to an enhanced efflux of K+ into the lumen and a reduced K+ efflux to the serosal compartment.
摘要
  1. 通过测量大鼠远端结肠黏膜 - 黏膜下层制剂中铷(Rb⁺)的单向通量、摄取和流出,并对分离隐窝的隐窝上皮进行膜片钳实验,研究了环磷酸腺苷(cAMP)途径激动剂和293B(一种色满醇衍生的钾通道阻滞剂)对大鼠远端结肠钾转运的影响。2. 293B呈浓度依赖性地抑制基础和福斯高林刺激的短路电流。在分离的隐窝中,293B阻断基础钾电导,但对顶端氯离子通道开放诱导的cAMP诱发的去极化无影响。当用葡萄糖酸盐替代氯离子以阻止cAMP对氯离子电导的影响时,福斯高林和一种膜通透性cAMP类似物对总细胞钾电导的抑制作用被揭示出来。3. 单向离子通量测量表明,293B抑制福斯高林诱导的黏膜 - 黏膜下层铷通量增加。这与对cAMP诱导的阴离子分泌的抑制一起表明,该药物阻断钾通道,可能在顶端和基底外侧膜中均有阻断作用。福斯高林不仅引起钾吸收的抑制,还刺激钾分泌。在存在顶端氢钾ATP酶抑制剂钒酸盐和哇巴因的情况下,抑制作用减弱但未被阻断。福斯高林刺激浆膜侧布美他尼敏感的铷摄取,而黏膜侧哇巴因/钒酸盐敏感的摄取不受影响。4. 流出实验表明,福斯高林导致细胞钾流出重新分布,降低了基底外侧与顶端铷流出的比率。5. 这些结果表明,细胞内环磷酸腺苷通过多种机制对钾转运发挥作用:由于氯离子通道开放诱导的去极化导致钾流出驱动力增加;通过钠钾氯共转运体刺激基底外侧钾摄取;以及基底外侧与顶端钾电导比率降低,导致钾向肠腔的流出增强,向浆膜腔的钾流出减少。

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