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大鼠S1近端小管中氨生成酶适应性的解离与铵排泄反应

Dissociation of ammoniagenic enzyme adaptation in rat S1 proximal tubules and ammonium excretion response.

作者信息

DiGiovanni S R, Madsen K M, Luther A D, Knepper M A

机构信息

Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Am J Physiol. 1994 Sep;267(3 Pt 2):F407-14. doi: 10.1152/ajprenal.1994.267.3.F407.

Abstract

We measured ammonium production rates, phosphate-dependent glutaminase (PDG) activity, and glutamate dehydrogenase (GDH) activity in microdissected S1 proximal tubules of rats to investigate the role of adaptations of PDG activity and GDH activity in response to a step increase in acid intake. In vivo ammonium excretion increased much more rapidly than did single-tubule ammonium production in vitro or ammoniagenic enzyme activities measured in microdissected tubules, manifesting an 85-fold increase in the first 24 h. In vitro ammonium production rates in microdissected tubules rose only twofold in the first 24 h, fourfold by day 2, and fivefold by day 4 of acid loading. The adaptation of PDG activity paralleled the increase in single-tubule ammoniagenic capacity measured in vitro. GDH activity, on the other hand, did not change significantly even after 4 days of acid loading. From these observations, we conclude that 1) the adaptation of in vitro ammoniagenic capacity in S1 proximal tubules is temporally associated with an adaptation in PDG activity and not GDH activity, and 2) a major portion of the increased ammonium excretion seen in the first 24 h is due to factors other than an adaptive increase in ammoniagenic enzyme activity.

摘要

我们测定了大鼠微切割S1近端小管中的铵生成速率、磷酸依赖性谷氨酰胺酶(PDG)活性和谷氨酸脱氢酶(GDH)活性,以研究PDG活性和GDH活性的适应性变化在酸摄入量逐步增加时所起的作用。与体外单小管铵生成或微切割小管中测得的产氨酶活性相比,体内铵排泄增加得更快,在最初24小时内增加了85倍。微切割小管的体外铵生成速率在酸负荷的最初24小时仅增加了两倍,到第2天增加了四倍,到第4天增加了五倍。PDG活性的适应性变化与体外测得的单小管产氨能力的增加平行。另一方面,即使在酸负荷4天后,GDH活性也没有显著变化。从这些观察结果中,我们得出结论:1)S1近端小管体外产氨能力的适应性变化在时间上与PDG活性的适应性变化相关,而非GDH活性;2)在最初24小时内观察到的铵排泄增加的主要部分是由于产氨酶活性适应性增加以外的因素。

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