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

Author:

Lee Hyun-Wook1,Osis Gunars1,Handlogten Mary E.1,Verlander Jill W.1ORCID,Weiner I. David12ORCID

Affiliation:

1. Division of Nephrology, Hypertension and Transplantation, University of Florida College of Medicine, Gainesville, Florida; and

2. Nephrology and Hypertension Section, North Florida/South Georgia Veterans Health System, Gainesville, Florida

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.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

U.S. Department of Veterans Affairs (VA)

Publisher

American Physiological Society

Subject

Physiology

Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Acid-base effects of combined renal deletion of NBCe1-A and NBCe1-B;American Journal of Physiology-Renal Physiology;2022-02-01

2. Role of the renal androgen receptor in sex differences in ammonia metabolism;American Journal of Physiology-Renal Physiology;2021-11-01

3. Expression of lactate dehydrogenase A and B isoforms in the mouse kidney;American Journal of Physiology-Renal Physiology;2021-05-01

4. Amino Acids | Glutamine;Encyclopedia of Biological Chemistry III;2021

5. Novel aspects of glutamine synthetase in ammonia homeostasis;Neurochemistry International;2020-11

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3