Gazitúa S, Robinson J W
Pflugers Arch. 1982 Jul;394(1):32-7. doi: 10.1007/BF01108305.
The unidirectional fluxes of sodium and chloride across stripped rat colon mucosa were measured and compared with the electrical characteristics of the tissue under voltage-clamped conditions. The relationship between the serosal-mucosal fluxes of the two ions and an imposed potential revealed that the serosal-mucosal flux of sodium was entirely paracellular, whereas there was also a transcellular component of the corresponding chloride flux. In the absence of sodium, the short-circuit current and net chloride flux were abolished; in the absence of chloride, the net sodium flux was reduced but not abolished, and the short-circuit current was unchanged. From an analysis of the effects of the inhibitors, amiloride, theophylline, acetazolamide, furosemide and piretanide, a plausible model was developed to explain the characteristics of these transports. It was proposed that both membranes possess Cl-/HCO-3 antiports, though their sensitivities to inhibitors were different. There is also a Na+/Cl- symport and an electrogenic sodium entry mechanism in the brushborder membrane.
测定了钠和氯跨剥离大鼠结肠黏膜的单向通量,并将其与电压钳制条件下组织的电特性进行了比较。两种离子的浆膜-黏膜通量与施加电位之间的关系表明,钠的浆膜-黏膜通量完全是细胞旁的,而相应的氯通量也有一个跨细胞成分。在无钠的情况下,短路电流和净氯通量消失;在无氯的情况下,净钠通量降低但未消失,短路电流不变。通过对抑制剂氨氯吡脒、茶碱、乙酰唑胺、呋塞米和吡咯他尼作用的分析,建立了一个合理的模型来解释这些转运的特性。有人提出,虽然两种膜对抑制剂的敏感性不同,但都具有Cl-/HCO-3反向转运体。刷状缘膜中也存在Na+/Cl-同向转运体和生电钠进入机制。