Hays S, Kokko J P, Jacobson H R
J Clin Invest. 1986 Nov;78(5):1279-86. doi: 10.1172/JCI112712.
With the exception of aldosterone, little is known about the hormonal regulation of distal nephron acidification. These experiments investigated the effects of prostaglandin E2, indomethacin, lysyl-bradykinin, 8-bromo-cyclic AMP, and forskolin on proton secretion in the major acidifying segment of the distal nephron, the medullary collecting duct from inner stripe of outer medulla. Using in vitro microperfusion and microcalorimetry, net bicarbonate reabsorption (proton secretion) was measured in rabbit medullary collecting ducts before, during, and after exposure to each test substance. PGE2 reduced proton secretion 12.2%, while the following substances stimulated proton secretion: indomethacin 14.2%; 8-bromo-cyclic AMP 34.5%; forskolin 39%. Lysyl-bradykinin was without effect. These studies demonstrate that distal nephron acidification, in addition to being stimulated by aldosterone, is significantly inhibited by the hormone PGE2. The stimulation of proton secretion by cAMP suggests that other hormones known to activate adenylate cyclase may also influence distal nephron acidification.
除醛固酮外,对于远曲小管酸化的激素调节知之甚少。这些实验研究了前列腺素E2、消炎痛、赖氨酰缓激肽、8-溴环磷酸腺苷和福斯高林对远曲小管主要酸化节段(外髓质内带髓质集合管)质子分泌的影响。采用体外微灌注和微量量热法,在兔髓质集合管暴露于每种测试物质之前、期间和之后测量净碳酸氢盐重吸收(质子分泌)。前列腺素E2使质子分泌减少12.2%,而以下物质刺激质子分泌:消炎痛14.2%;8-溴环磷酸腺苷34.5%;福斯高林39%。赖氨酰缓激肽无作用。这些研究表明,远曲小管酸化除受醛固酮刺激外,还受到激素前列腺素E2的显著抑制。环磷酸腺苷对质子分泌的刺激表明,已知能激活腺苷酸环化酶的其他激素也可能影响远曲小管酸化。