Sellin J H, DeSoignie R
Am J Physiol. 1984 May;246(5 Pt 1):G603-10. doi: 10.1152/ajpgi.1984.246.5.G603.
Rabbit proximal colon (PC), examined in vitro, exhibits transport characteristics distinct from distal colon. Unlike distal colon, PC does not demonstrate amiloride-inhibitable electrogenic Na absorption. Additionally, neither amphotericin nor "stimulatory" anions induce Na absorption in PC. Electrical measurements and radioisotopic flux studies under short-circuit conditions indicate that PC is a moderately leaky epithelium with a conductance (9.0 +/- 0.2 mS) midway between ileum and distal colon; under basal conditions PC has Na and Cl transport rates near zero, and 5.5 microM epinephrine (Epi) stimulates electrically silent Na-Cl coupled absorption. The mechanism of this cotransport was investigated further: Cl substitution with either sulfate or gluconate did not substantially alter Epi-enhanced Na absorption. The Epi stimulation of Cl absorption in a Na-free solution was diminished. Amiloride, 10(-3) M, inhibited Epi-enhanced Na absorption by approximately 50%. The effects of cAMP-mediated (theophylline or 8-bromo-cAMP) and Ca-mediated (ionophore A23187) secretory stimuli were examined. In the basal state, none of these agents had a consistent effect on ion transport. However, after stimulation of Na and Cl absorption by Epi, both of the cAMP-related secretagogues had a marked antiabsorptive effect on Na and Cl transport. The antiabsorptive effects of Ca ionophore A23187 were less marked. These results suggest that rabbit proximal colon a) does not share the transport properties characteristic of distal colon, b) possesses an Epi-sensitive, Na-Cl-coupled absorptive pathway, and c) responds to secretory stimuli in an antiabsorptive manner rather than by electrogenic secretion.
对兔近端结肠(PC)进行的体外研究显示,其转运特性与远端结肠不同。与远端结肠不同,近端结肠不表现出氨氯吡脒抑制的电中性钠吸收。此外,两性霉素和“刺激性”阴离子均不能诱导近端结肠的钠吸收。短路条件下的电学测量和放射性同位素通量研究表明,近端结肠是一种中等渗漏的上皮组织,其电导(9.0±0.2 mS)介于回肠和远端结肠之间;在基础条件下,近端结肠的钠和氯转运速率接近零,5.5微摩尔肾上腺素(Epi)可刺激电沉默的钠-氯偶联吸收。进一步研究了这种协同转运的机制:用硫酸盐或葡萄糖酸盐替代氯并不会显著改变Epi增强的钠吸收。在无钠溶液中,Epi对氯吸收的刺激作用减弱。10⁻³ M的氨氯吡脒抑制Epi增强的钠吸收约50%。研究了环磷酸腺苷(cAMP)介导的(茶碱或8-溴-cAMP)和钙介导的(离子载体A23187)分泌刺激的作用。在基础状态下,这些试剂对离子转运均无一致的影响。然而,在用Epi刺激钠和氯吸收后,两种与cAMP相关的促分泌剂对钠和氯转运均有显著的抗吸收作用。钙离子载体A23187的抗吸收作用则不太明显。这些结果表明,兔近端结肠a)不具有远端结肠特有的转运特性,b)具有对Epi敏感的钠-氯偶联吸收途径,c)对分泌刺激的反应是抗吸收而非电中性分泌。