Argenzio R A, Whipp S C
Can J Physiol Pharmacol. 1983 Oct;61(10):1138-48. doi: 10.1139/y83-170.
The effect of theophylline and a heat-stable enterotoxin of Escherichia coli (ST) on ion transport was examined using an in vitro, short-circuited preparation of the porcine colon. Theophylline abolished net Na absorption and elicited net Cl secretion, which quantitatively accounted for the increase in short-circuit current (Isc) observed. In contrast, a maximal dose of ST elicited an Isc response about one-half that of theophylline and only partially reduced the net absorption of Na and Cl. A significant residual ion flux, consistent with HCO3 secretion, was elicited by ST and was sustained after theophylline addition. Ion replacement experiments showed that the Isc and net ion transport response to ST was abolished when either Cl or HCO3 were removed from the bathing solutions. Voltage clamp experiments to evaluate the contribution of the paracellular and transcellular transepithelial pathways from serosa to mucosa showed that approximately one-half of the total serosa-to-mucosa flux (Jsm) of both Na and Cl was through the cells. Theophylline and ST both significantly reduced transcellular JNasm, but did not affect JClsm. Theophylline, but not ST, caused an increase in paracellular conductance of both ions. These results demonstrate significant differences in the effects of ST or theophylline on both transcellular and paracellular ion movement, and suggest that ST induces a Cl-dependent HCO3 secretion which is unobserved under control or theophylline-stimulated conditions. In addition, results are consistent with the operation of a neutral NaCl secretory process which is normally masked by the greater net rates of the neutral Na and Cl absorptive mechanisms. Thus, both ST and theophylline appear to reduce or abolished the neutral processes and convert the neutral secretory process into an electrogenic one. This latter effect could be explained simply by an increase in the anion conductance of the mucosal membranes.
利用猪结肠体外短路制备模型,研究了茶碱和大肠杆菌热稳定肠毒素(ST)对离子转运的影响。茶碱消除了净钠吸收并引发了净氯分泌,这在数量上解释了所观察到的短路电流(Isc)增加。相比之下,最大剂量的ST引发的Isc反应约为茶碱的一半,且仅部分降低了钠和氯的净吸收。ST引发了与碳酸氢根分泌一致的显著残余离子通量,且在添加茶碱后仍持续存在。离子置换实验表明,当从浴液中去除氯或碳酸氢根时,对ST的Isc和净离子转运反应均被消除。电压钳实验评估了从浆膜到黏膜的细胞旁和跨细胞上皮途径的贡献,结果显示钠和氯的总浆膜到黏膜通量(Jsm)中约有一半是通过细胞的。茶碱和ST均显著降低跨细胞JNasm,但不影响JClsm。茶碱而非ST导致两种离子的细胞旁电导增加。这些结果表明ST或茶碱对跨细胞和细胞旁离子运动的影响存在显著差异,并提示ST诱导了一种依赖氯的碳酸氢根分泌,这在对照或茶碱刺激条件下未观察到。此外,结果与一种中性氯化钠分泌过程的运作一致,该过程通常被更大的中性钠和氯吸收机制的净速率所掩盖。因此,ST和茶碱似乎都降低或消除了中性过程,并将中性分泌过程转化为电生过程。后一种效应可以简单地通过黏膜膜阴离子电导的增加来解释。