Ahn J, Chang E B, Field M
Am J Physiol. 1985 Nov;249(5 Pt 1):C527-30. doi: 10.1152/ajpcell.1985.249.5.C527.
In rabbit proximal colon, in vitro addition of phorbol 12,13-dibutyrate (PDB, 10(-7) M) to the serosal bathing medium inhibits mucosal (m)-to-serosal (s) unidirectional Na flux (JsmNa) without altering JsmNa or unidirectional Cl fluxes. Similar results were obtained when amiloride (2 X 10(-4) M) was added to the mucosal bathing medium. No additivity of effect was seen when tissues were exposed to both agents. Measurements with carboxyfluorescein reveal that the two agents cause equal decreases of intracellular pH (pHi), an effect that is dependent on the presence of extracellular Na (Na replacement also decreases pHi). No additivity of pHi effects is seen when both agents are added together. To determine the membrane site of this PDB-inhibitable Na-H exchange, Na influx across the luminal border of proximal colon was measured and was found to be inhibited equally by PDB and amiloride. We conclude that PDB, by activation of protein kinase C, inhibits electro-neutral amiloride-sensitive Na-H exchange in the luminal membrane of proximal colon.
在兔近端结肠中,向浆膜侧浴液中体外添加佛波醇12,13 - 二丁酸酯(PDB,10⁻⁷ M)可抑制黏膜(m)到浆膜(s)的单向钠通量(JsmNa),而不改变JsmNa或单向氯通量。当向黏膜侧浴液中添加氨氯吡脒(2×10⁻⁴ M)时,也得到了类似结果。当组织同时暴露于这两种药物时,未观察到效应的相加性。用羧基荧光素测量发现,这两种药物可使细胞内pH(pHi)同等程度降低,这种效应依赖于细胞外钠的存在(钠替代也会降低pHi)。当同时添加这两种药物时,未观察到pHi效应的相加性。为了确定这种PDB可抑制的钠 - 氢交换的膜位点,测量了近端结肠腔面边界的钠内流,发现其同样受到PDB和氨氯吡脒的抑制。我们得出结论,PDB通过激活蛋白激酶C,抑制近端结肠腔面膜中电中性的氨氯吡脒敏感的钠 - 氢交换。