Kidney-specific KO of the circadian clock protein PER1 alters renal Na+ handling, aldosterone levels, and kidney/adrenal gene expression

被引:19
作者
Douma, Lauren G. [1 ,2 ,3 ]
Costello, Hannah M. [1 ,2 ]
Crislip, G. Ryan [1 ,2 ]
Cheng, Kit-Yan [1 ,2 ]
Lynch, I. Jeanette [2 ,4 ]
Juffre, Alexandria [1 ,2 ,3 ]
Barral, Dominique [2 ]
Masten, Sarah [2 ]
Roig, Emilio [2 ]
Beguiristain, Kevin [2 ]
Li, Wendy [2 ]
Bratanatawira, Phillip [2 ]
Wingo, Charles S. [2 ,4 ]
Gumz, Michelle L. [1 ,2 ,3 ,5 ]
机构
[1] Univ Florida, Dept Physiol & Funct Genom, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Med, Div Nephrol Hypertens & Renal Transplantat, Gainesville, FL 32611 USA
[3] Univ Florida, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
[4] North Florida South Georgia Malcolm Randall Vet A, Gainesville, FL USA
[5] Univ Florida, Ctr Integrat Cardiovasc & Metab Dis, Gainesville, FL 32611 USA
关键词
circadian rhythm; homeostasis; salt; sodium; SODIUM-CHANNEL; BLOOD-PRESSURE; HYPERTENSION; SALT; KNOCKOUT; RATIO; ENAC;
D O I
10.1152/ajprenal.00385.2021
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
PERIOD 1 (PER1) is a circadian clock transcription factor that is regulated by aldosterone, a hormone that increases blood volume and Na+ retention to increase blood pressure. Male global Per1 knockout (KO) mice develop reduced night/day differences in Na+ excretion in response to a high-salt diet plus desoxycorticosterone pivalate treatment (HS + DOCP), a model of salt-sensitive hypertension. In addition, global Per1 KO mice exhibit higher aldosterone levels on a normal-salt diet. To determine the role of Per1 in the kidney, male kidney-specific Per1 KO (KS-Per1 KO) mice were generated using Ksp-cadherin Cre recombinase to remove exons 2-8 of Per1 in the distal nephron and collecting duct. Male KS-Per1 KO mice have increased Na+ retention but have normal diurnal differences in Na+ excretion in response to HS + DOCP. The increased Na+ retention is associated with altered expression of glucocorticoid and mineralocorticoid receptors, increased serum aldosterone, and increased medullary endothelin-1 compared with control mice. Adrenal gland gene expression analysis revealed that circadian clock and aldosterone synthesis genes have altered expression in KS-Per1 KO mice compared with control mice. These results emphasize the importance of the circadian clock not only in maintaining rhythms of physiological functions but also for adaptability in response to environmental cues, such as HS + DOCP, to maintain overall homeostasis. Given the prevalence of salt-sensitive hypertension in the general population, these findings have important implications for our understanding of how circadian clock proteins regulate homeostasis. NEW & NOTEWORTHY For the first time, we show that knockout of the circadian clock transcription factor PERIOD 1 using kidney-specific cadherin Cre results in increased renal Na+ reabsorption, increased aldosterone levels, and changes in gene expression in both the kidney and adrenal gland. Diurnal changes in renal Na+ excretion were not observed, demonstrating that the clock protein PER1 in the kidney is important for maintaining homeostasis and that this effect may be independent of time of day.
引用
收藏
页码:F449 / F459
页数:11
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