Nonoguchi H, Takehara Y, Endou H
Pflugers Arch. 1986 Sep;407(3):245-51. doi: 10.1007/BF00585298.
In order to determine intra- and inter-nephron heterogeneity of ammoniagenesis, ammoniagenic activity in microdissected nephron segments of control, acidotic and potassium (K)-depleted rats was examined. Intranephron distribution of ammoniagenic activity in control rats revealed the highest amount at the second segment of the proximal tubule (S2). Chronic metabolic acidosis induced ammoniagenesis markedly at the first segment of the proximal tubule (S1) by 235% and the thick ascending limb of Henle's loop by 198% and moderately at the S2 by 49%. K-depletion increased ammonia production significantly in the S1 by 298% and the S2 by 107%, which is a pattern quite similar to the result of chronic metabolic acidosis. Ammonia production in K-depletion was also increased in the cortical and medullary collecting tubule by 71% and 102%, respectively, probably due to increases in protein amounts (41% and 158%, respectively) there. To evaluate inter-nephron heterogeneity of ammoniagenesis, ammonia formation from glutamine in the S1 of superficial (SF) and juxtamedullary (JM) nephrons was examined. Although there was no difference in ammonia production between SF-S1 and JM-S1 in control rats, ammonia production in SF-S1 was significantly higher than that in JM-S1 in both metabolic acidosis and K-depletion. From these studies, we conclude: The increase of ammonia production in the proximal tubule was quite similar in both acidosis and K-depletion, suggesting that the main trigger of ammoniagenesis in both conditions might be a reduction of intracellular pH. SF-S1 was the nephron most reactive to acidosis and K-depletion. JM nephrons could be considered to be important not for ammonia production but for ammonia secretion.
为了确定肾单位内和肾单位间氨生成的异质性,我们检测了对照、酸中毒和低钾大鼠显微解剖的肾单位节段中的氨生成活性。对照大鼠肾单位内氨生成活性的分布显示,近端小管第二段(S2)的活性最高。慢性代谢性酸中毒使近端小管第一段(S1)的氨生成显著增加235%,亨氏袢厚升支的氨生成增加198%,S2段的氨生成中度增加49%。低钾血症使S1段的氨生成显著增加298%,S2段增加107%,这一模式与慢性代谢性酸中毒的结果非常相似。低钾血症时,皮质和髓质集合管的氨生成也分别增加了71%和102%,这可能是由于那里的蛋白量分别增加了41%和158%。为了评估氨生成的肾单位间异质性,我们检测了浅表肾单位(SF)和近髓肾单位(JM)S1段谷氨酰胺生成氨的情况。尽管对照大鼠的SF-S1和JM-S1之间的氨生成没有差异,但在代谢性酸中毒和低钾血症时,SF-S1的氨生成均显著高于JM-S1。从这些研究中,我们得出结论:酸中毒和低钾血症时近端小管氨生成的增加非常相似,这表明在这两种情况下氨生成的主要触发因素可能是细胞内pH值的降低。SF-S1是对酸中毒和低钾血症反应最敏感的肾单位。JM肾单位可能不是主要参与氨的生成,而是参与氨的分泌。