Literature DB >> 28331060

Proximal tubule glutamine synthetase expression is necessary for the normal response to dietary protein restriction.

Hyun-Wook Lee1, Gunars Osis1, Mary E Handlogten1, Jill W Verlander1, I David Weiner2,3.   

Abstract

Dietary protein restriction has multiple benefits in kidney disease. Because protein intake is a major determinant of endogenous acid production, it is important that net acid excretion changes in parallel during changes in dietary protein intake. Dietary protein restriction decreases endogenous acid production and decreases urinary ammonia excretion, a major component of net acid excretion. Glutamine synthetase (GS) catalyzes the reaction of [Formula: see text] and glutamate, which regenerates the essential amino acid glutamine and decreases net ammonia generation. Because renal proximal tubule GS expression increases during dietary protein restriction, this could contribute to the decreased ammonia excretion. The purpose of the current study was to determine the role of proximal tubule GS in the renal response to protein restriction. We generated mice with proximal tubule-specific GS deletion (PT-GS-KO) using Cre-loxP techniques. Cre-negative (Control) and PT-GS-KO mice in metabolic cages were provided 20% protein diet for 2 days and were then changed to low-protein (6%) diet for the next 7 days. Additional PT-GS-KO mice were maintained on 20% protein diet. Dietary protein restriction caused a rapid decrease in urinary ammonia excretion in both genotypes, but PT-GS-KO blunted this adaptive response significantly. This occurred despite no significant genotype-dependent differences in urinary pH or in serum electrolytes. There were no significant differences between Control and PT-GS-KO mice in expression of multiple other proteins involved in renal ammonia handling. We conclude that proximal tubule GS expression is necessary for the appropriate decrease in ammonia excretion during dietary protein restriction.

Entities:  

Keywords:  acid-base; ammonia; dietary protein; proximal tubule

Mesh:

Substances:

Year:  2017        PMID: 28331060      PMCID: PMC5538840          DOI: 10.1152/ajprenal.00048.2017

Source DB:  PubMed          Journal:  Am J Physiol Renal Physiol        ISSN: 1522-1466


  42 in total

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5.  Localization of ammonia-metabolizing enzymes in human liver: ontogenesis of heterogeneity.

Authors:  A F Moorman; J L Vermeulen; R Charles; W H Lamers
Journal:  Hepatology       Date:  1989-03       Impact factor: 17.425

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8.  Proximal tubule-specific glutamine synthetase deletion alters basal and acidosis-stimulated ammonia metabolism.

Authors:  Hyun-Wook Lee; Gunars Osis; Mary E Handlogten; Wouter H Lamers; Farrukh A Chaudhry; Jill W Verlander; I David Weiner
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9.  An analysis of regulatory elements in the phosphoenolpyruvate carboxykinase (GTP) gene which are responsible for its tissue-specific expression and metabolic control in transgenic mice.

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4.  Acid-base effects of combined renal deletion of NBCe1-A and NBCe1-B.

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5.  NBCe1-A Regulates Proximal Tubule Ammonia Metabolism under Basal Conditions and in Response to Metabolic Acidosis.

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7.  Expression of lactate dehydrogenase A and B isoforms in the mouse kidney.

Authors:  Gunars Osis; Amie M Traylor; Laurence M Black; Daryll Spangler; James F George; Abolfazl Zarjou; Jill W Verlander; Anupam Agarwal
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8.  Role of the renal androgen receptor in sex differences in ammonia metabolism.

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