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本文引用的文献

1
High dietary sodium causes dyssynchrony of the renal molecular clock in rats.高膳食钠导致大鼠肾脏分子钟失同步。
Am J Physiol Renal Physiol. 2018 Jan 1;314(1):F89-F98. doi: 10.1152/ajprenal.00028.2017. Epub 2017 Sep 27.
2
Timing the day: what makes bacterial clocks tick?一天的计时:是什么让细菌时钟滴答作响?
Nat Rev Microbiol. 2017 Apr;15(4):232-242. doi: 10.1038/nrmicro.2016.196. Epub 2017 Feb 20.
3
Chronotherapy for hypertension in patients with chronic kidney disease: a systematic review and meta-analysis in non-black patients.慢性肾脏病患者高血压的时间疗法:非黑人患者的系统评价和荟萃分析
Int Urol Nephrol. 2017 Apr;49(4):651-659. doi: 10.1007/s11255-016-1437-2. Epub 2016 Nov 14.
4
Desoxycorticosterone pivalate-salt treatment leads to non-dipping hypertension in Per1 knockout mice.去氧皮质酮新戊酸酯盐治疗导致Per1基因敲除小鼠出现非勺型高血压。
Acta Physiol (Oxf). 2017 May;220(1):72-82. doi: 10.1111/apha.12804. Epub 2016 Oct 3.
5
Loss of endothelin B receptor function impairs sodium excretion in a time- and sex-dependent manner.内皮素B受体功能丧失会以时间和性别依赖的方式损害钠排泄。
Am J Physiol Renal Physiol. 2016 Nov 1;311(5):F991-F998. doi: 10.1152/ajprenal.00103.2016. Epub 2016 Aug 31.
6
Nocturnal Hypertension: Neglected Issue in Comprehensive Hypertension Management.夜间高血压:综合高血压管理中被忽视的问题。
Acta Med Indones. 2016 Jan;48(1):76-82.
7
Nephron-Specific Deletion of Circadian Clock Gene Bmal1 Alters the Plasma and Renal Metabolome and Impairs Drug Disposition.肾单位特异性敲除生物钟基因Bmal1会改变血浆和肾脏代谢组并损害药物处置。
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8
Circadian Rhythms, Metabolism, and Chrononutrition in Rodents and Humans.啮齿动物和人类的昼夜节律、新陈代谢与时间营养学
Adv Nutr. 2016 Mar 15;7(2):399-406. doi: 10.3945/an.115.010777. Print 2016 Mar.
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Endothelin.内皮素
Pharmacol Rev. 2016 Apr;68(2):357-418. doi: 10.1124/pr.115.011833.
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Endothelin and renal ion and water transport.内皮素与肾脏离子及水的转运。
Semin Nephrol. 2015 Mar;35(2):137-44. doi: 10.1016/j.semnephrol.2015.02.003.

生物钟对肾功能的调节作用:Bmal1 的作用研究

Circadian regulation of kidney function: finding a role for Bmal1.

机构信息

Section of Cardio-Renal Physiology and Medicine, Division of Nephrology, Department of Medicine, University of Alabama at Birmingham , Birmingham, Alabama.

出版信息

Am J Physiol Renal Physiol. 2018 May 1;314(5):F675-F678. doi: 10.1152/ajprenal.00580.2017. Epub 2017 Dec 20.

DOI:10.1152/ajprenal.00580.2017
PMID:29357439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6031908/
Abstract

Mounting evidence suggests that there is an internal molecular "clock" within the kidney to help maintain normal renal function. Disturbance of the kidney circadian rhythm may pose a threat to water and electrolyte homeostasis and blood pressure regulation, among many other problems. The identification of circadian genes facilitated a more comprehensive appreciation of the importance of "keeping the body on time"; however, our knowledge is very limited with regard to how circadian genes regulate kidney function. In this brief review, we summarize recent progress in circadian control of renal physiology, with a particular focus on aryl hydrocarbon receptor nuclear translocator-like protein (Arntl1; also called Bmal1).

摘要

越来越多的证据表明,肾脏内部存在一种内在的分子“时钟”,有助于维持正常的肾功能。肾脏昼夜节律的紊乱可能对水和电解质平衡以及血压调节等诸多问题构成威胁。昼夜节律基因的鉴定使人们更全面地认识到“保持身体的时间同步性”的重要性;然而,我们对于昼夜节律基因如何调节肾脏功能的了解还非常有限。在这篇简要的综述中,我们总结了肾脏生理学昼夜节律控制的最新进展,特别关注芳香烃受体核转位蛋白样蛋白 (Arntl1;也称为 Bmal1)。