McLaughlin M L, McBride D E, Perrone R D
Department of Medicine, New England Medical Center, Tufts University School of Medicine, Boston, MA 02111.
Pflugers Arch. 1990 Aug;416(6):639-45. doi: 10.1007/BF00370608.
Recent studies from this laboratory have determined that colonic K+ absorption is altered by the PCO2 and by secondary hyperaldosteronism. Partial inhibition by vanadate and mucosal ouabain suggested the operation of an H+/K+ exchange pump. To determine the mechanism of acidification in rat distal colon, we measured in vitro acidification using the pH-stat technique by voltage-clamped segments of colonic epithelium in controls and in the presence of secondary hyperaldosteronism, induced by a sodium-deficient diet. Chronic stimulation with aldosterone resulted in increased mucosal acidification in vitro for at least 2 h. This effect could not be accounted for by lactate production and was not altered by elimination of the aldosterone-induced increase in voltage and short-circuit current with 10 microM amiloride. Studies with inhibitors and ion substitution revealed that mucosal acidification resulted from both Na-dependent and Na-independent mechanisms. Na-dependent acidification was inhibited by ATPase inhibitors and was mediated in part by a luminal Na+/H+ exchanger in the presence of secondary hyperaldosteronism. Na-independent acidification was mediated by a pathway dependent on luminal K+ that was inhibited by vanadate and mucosal ouabain, consistent with the operation of an H+/K+ exchange pump.
本实验室最近的研究已确定,结肠钾离子吸收会因二氧化碳分压和继发性醛固酮增多症而改变。钒酸盐和黏膜哇巴因的部分抑制作用提示存在氢离子/钾离子交换泵。为确定大鼠远端结肠酸化的机制,我们采用pH计技术,通过电压钳制结肠上皮片段,在对照组以及由缺钠饮食诱导的继发性醛固酮增多症模型中,测量体外酸化情况。长期用醛固酮刺激导致体外黏膜酸化至少持续2小时。这种效应不能用乳酸生成来解释,并且用10微摩尔阿米洛利消除醛固酮诱导的电压和短路电流增加后,该效应并未改变。使用抑制剂和离子替代的研究表明,黏膜酸化是由钠依赖性和非钠依赖性机制共同导致的。钠依赖性酸化被ATP酶抑制剂抑制,并且在继发性醛固酮增多症存在时,部分由管腔钠离子/氢离子交换体介导。非钠依赖性酸化由一条依赖管腔钾离子的途径介导,该途径被钒酸盐和黏膜哇巴因抑制,这与氢离子/钾离子交换泵的作用一致。