Sandle G I, McNicholas C M, Lomax R B
Department of Medicine, Hope Hospital (University of Manchester, School of Medicine, Salford, UK.
Lancet. 1994 Jan 1;343(8888):23-5. doi: 10.1016/s0140-6736(94)90878-8.
A characteristic feature of intestinal epithelia is their ability to secrete chloride (Cl-), a process that occurs mainly in intestinal crypts and is the critical transport event in secretory diarrhoea. Increased potassium (K+) channel activity in the basolateral membrane has an important role in the Cl- secretory process by hyperpolarising the cell and maintaining a favourable electrochemical driving force for Cl- exit at the apical membrane. We have shown, using patch-clamp techniques, that the basolateral membrane of human colonic crypt cells contains low conductance K+ channels that are voltage and calcium (Ca2+) sensitive and blocked by barium (Ba2+). These K+ channels are regulated by cytosolic cyclic adenosine monophosphate (cAMP) and Ca2+, intracellular second messengers that also stimulate Cl- secretion. This population of human intestinal K+ channels may be a target for the pharmacological control of Cl- secretory diarrhoea.
肠道上皮细胞的一个特征是它们分泌氯离子(Cl-)的能力,这一过程主要发生在肠道隐窝,是分泌性腹泻中的关键转运事件。基底外侧膜上钾离子(K+)通道活性增加,通过使细胞超极化并维持顶端膜上氯离子流出的有利电化学驱动力,在氯离子分泌过程中发挥重要作用。我们使用膜片钳技术表明,人结肠隐窝细胞的基底外侧膜含有低电导钾离子通道,这些通道对电压和钙离子(Ca2+)敏感,并被钡离子(Ba2+)阻断。这些钾离子通道受胞质环磷酸腺苷(cAMP)和钙离子调节,这两种细胞内第二信使也会刺激氯离子分泌。这群人肠道钾离子通道可能是氯离子分泌性腹泻药物控制的靶点。