• Natsuko Tokonami, David Mordasini, Sylvain Pradervand, Gabriel Centeno, Céline Jouffe, Marc Maillard, Olivier Bonny, Frédéric Gachon, R Ariel Gomez, Maria Luisa S Sequeira-Lopez, and Dmitri Firsov.
• Department of Pharmacology and Toxicology and.
• J. Am. Soc. Nephrol. 2014 Jul 1;25(7):1430-9.

AbstractThe circadian timing system is critically involved in the maintenance of fluid and electrolyte balance and BP control. However, the role of peripheral circadian clocks in these homeostatic mechanisms remains unknown. We addressed this question in a mouse model carrying a conditional allele of the circadian clock gene Bmal1 and expressing Cre recombinase under the endogenous Renin promoter (Bmal1(lox/lox)/Ren1(d)Cre mice). Analysis of Bmal1(lox/lox)/Ren1(d)Cre mice showed that the floxed Bmal1 allele was excised in the kidney. In the kidney, BMAL1 protein expression was absent in the renin-secreting granular cells of the juxtaglomerular apparatus and the collecting duct. A partial reduction of BMAL1 expression was observed in the medullary thick ascending limb. Functional analyses showed that Bmal1(lox/lox)/Ren1(d)Cre mice exhibited multiple abnormalities, including increased urine volume, changes in the circadian rhythm of urinary sodium excretion, increased GFR, and significantly reduced plasma aldosterone levels. These changes were accompanied by a reduction in BP. These results show that local renal circadian clocks control body fluid and BP homeostasis.Copyright © 2014 by the American Society of Nephrology.

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