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本文引用的文献

1
Differences in acidosis-stimulated renal ammonia metabolism in the male and female kidney.男女肾脏酸中毒刺激下的氨代谢差异。
Am J Physiol Renal Physiol. 2019 Oct 1;317(4):F890-F905. doi: 10.1152/ajprenal.00244.2019. Epub 2019 Aug 7.
2
Differences in renal ammonia metabolism in male and female kidney.男性和女性肾脏中氨代谢的差异。
Am J Physiol Renal Physiol. 2018 Aug 1;315(2):F211-F222. doi: 10.1152/ajprenal.00084.2018. Epub 2018 Mar 21.
3
NBCe1-A Regulates Proximal Tubule Ammonia Metabolism under Basal Conditions and in Response to Metabolic Acidosis.NBCe1-A 调节基础条件下及代谢性酸中毒反应中的近端肾小管氨代谢。
J Am Soc Nephrol. 2018 Apr;29(4):1182-1197. doi: 10.1681/ASN.2017080935. Epub 2018 Feb 26.
4
Adverse Effects of the Metabolic Acidosis of Chronic Kidney Disease.慢性肾脏病代谢性酸中毒的不良反应
Adv Chronic Kidney Dis. 2017 Sep;24(5):289-297. doi: 10.1053/j.ackd.2017.06.005.
5
Intracrine androgen biosynthesis, metabolism and action revisited.重新审视胞内雄激素生物合成、代谢和作用。
Mol Cell Endocrinol. 2018 Apr 15;465:4-26. doi: 10.1016/j.mce.2017.08.016. Epub 2017 Sep 1.
6
Prevalence of sexual dimorphism in mammalian phenotypic traits.哺乳动物表型特征中存在性二态性的普遍性。
Nat Commun. 2017 Jun 26;8:15475. doi: 10.1038/ncomms15475.
7
Ammonia Transporters and Their Role in Acid-Base Balance.氨转运体及其在酸碱平衡中的作用。
Physiol Rev. 2017 Apr;97(2):465-494. doi: 10.1152/physrev.00011.2016.
8
Expression of sodium-dependent dicarboxylate transporter 1 (NaDC1/SLC13A2) in normal and neoplastic human kidney.钠依赖性二羧酸转运蛋白1(NaDC1/SLC13A2)在正常和肿瘤性人肾中的表达
Am J Physiol Renal Physiol. 2017 Mar 1;312(3):F427-F435. doi: 10.1152/ajprenal.00559.2016. Epub 2016 Dec 7.
9
Roles of renal ammonia metabolism other than in acid-base homeostasis.肾脏氨代谢在酸碱平衡之外的作用。
Pediatr Nephrol. 2017 Jun;32(6):933-942. doi: 10.1007/s00467-016-3401-x. Epub 2016 May 12.
10
Androgen Receptor Structure, Function and Biology: From Bench to Bedside.雄激素受体的结构、功能与生物学:从实验室到临床
Clin Biochem Rev. 2016 Feb;37(1):3-15.

睾酮调节肾脏氨代谢。

Testosterone modulates renal ammonia metabolism.

机构信息

Deparment of Small Animal Clinical Science, University of Florida College of Veterinary Medicine, Gainesville, Florida.

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

出版信息

Am J Physiol Renal Physiol. 2020 Apr 1;318(4):F922-F935. doi: 10.1152/ajprenal.00560.2019. Epub 2020 Mar 2.

DOI:10.1152/ajprenal.00560.2019
PMID:32116019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7191448/
Abstract

There are substantial sex differences in renal structure and ammonia metabolism that correlate with differences in expression of proteins involved in ammonia generation and transport. This study determined the role of testis-derived testosterone in these differences. We studied 4-mo-old male C57BL/6 mice 4 and 8 wk after either bilateral orchiectomy (ORCH) or sham-operated control surgery and determined the effect of testosterone replacement to reverse the effects of ORCH. Finally, we determined the cellular expression of androgen receptor (AR), testosterone's canonical target receptor. ORCH decreased kidney and proximal tubule size, and testosterone replacement reversed this effect. ORCH increased ammonia excretion in a testosterone-dependent fashion; this occurred despite similar food intake, which is the primary component of endogenous acid production. ORCH increased expression of both phosphopyruvate, a major ammonia-generating protein, and Na-K-2Cl cotransporter, which mediates thick ascending limb ammonia reabsorption; these changes were reversed with testosterone replacement. Orchiectomy also decreased expression of Na/H exchanger isoform 3, which mediates proximal tubule ammonia secretion, in a testosterone-dependent pattern. Finally, ARs are expressed throughout the proximal tubule in both the male and female kidney. Testosterone, possibly acting through ARs, has dramatic effects on kidney and proximal tubule size and decreases ammonia excretion through its effects on several key proteins involved in ammonia metabolism.

摘要

肾脏结构和氨代谢存在显著的性别差异,这与参与氨生成和转运的蛋白质表达差异有关。本研究旨在确定睾丸源性睾酮在这些差异中的作用。我们研究了 4 月龄雄性 C57BL/6 小鼠双侧睾丸切除(ORCH)或假手术对照手术后 4 周和 8 周,以确定睾酮替代治疗对逆转 ORCH 作用的影响。最后,我们确定了雄激素受体(AR)的细胞表达,AR 是睾酮的典型靶受体。ORCH 降低了肾脏和近端小管的大小,而睾酮替代治疗逆转了这一效应。ORCH 以依赖于睾酮的方式增加了氨的排泄;尽管有相似的食物摄入,这是内源性酸生成的主要成分,但这种情况仍会发生。ORCH 增加了磷酸烯醇丙酮酸(一种主要的氨生成蛋白)和 Na-K-2Cl 共转运体的表达,后者介导厚升支段氨的重吸收;这些变化在睾酮替代治疗后得到逆转。ORCH 还以依赖于睾酮的方式降低了介导近端小管氨分泌的 Na/H 交换体 3 的表达。最后,AR 在雄性和雌性肾脏的整个近端小管中均有表达。睾酮可能通过 AR 发挥作用,对肾脏和近端小管的大小有显著影响,并通过其对参与氨代谢的几个关键蛋白的作用降低氨排泄。