Heintze K, Stewart C P, Frizzell R A
Am J Physiol. 1983 Apr;244(4):G357-65. doi: 10.1152/ajpgi.1983.244.4.G357.
Electrogenic, cAMP-mediated Cl secretion across rabbit descending colon in vitro is independent of the rate or presence of active Na absorption. Yet, several observations indicate that this process is Na dependent: a) Cl secretion requires the presence of Na in the serosal solution alone, b) the kinetics of Cl transport as a function of external Na concentration are virtually identical to the Cl concentration dependence, and c) exchange of cell Cl with isotopic Cl added to the serosal solution is inhibited by Na-free media and by addition of furosemide to the serosal solution; the diuretic also inhibits Cl secretion. These findings suggest that Cl entry into the secretory cells across the basolateral membrane is mediated by NaCl cotransport. Addition of ouabain to, or removal of K from, the serosal solution inhibits Cl secretion so that Na entering the secretory cell across the basolateral membrane may be returned to the serosal solution by the Na-K pump. Finally, increasing the K concentration of the serosal solution inhibits Cl secretion under short-circuit conditions. This appears to result from K-induced depolarization of the electrical potential difference across the apical membrane so that diffusional Cl exit from cell to mucosal solution is reduced.
体外兔降结肠中由电产生的、cAMP介导的Cl分泌独立于主动Na吸收的速率或存在情况。然而,一些观察结果表明该过程依赖于Na:a)Cl分泌仅需要在浆膜溶液中存在Na,b)作为外部Na浓度函数的Cl转运动力学实际上与对Cl浓度的依赖性相同,并且c)细胞Cl与添加到浆膜溶液中的同位素Cl的交换受到无Na培养基以及向浆膜溶液中添加呋塞米的抑制;该利尿剂也抑制Cl分泌。这些发现表明,Cl通过基底外侧膜进入分泌细胞是由NaCl共转运介导的。向浆膜溶液中添加哇巴因或从浆膜溶液中去除K会抑制Cl分泌,因此通过基底外侧膜进入分泌细胞的Na可能会通过Na-K泵返回浆膜溶液。最后,在短路条件下增加浆膜溶液的K浓度会抑制Cl分泌。这似乎是由于K诱导的顶膜跨膜电位差去极化,从而减少了Cl从细胞向粘膜溶液的扩散性流出。