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Sex differences in the adrenal circadian clock: A role for BMAL1 in the regulation of urinary aldosterone excretion and renal electrolyte balance in mice

内分泌学 内科学 醛固酮 皮质酮 昼夜节律 时钟 生物 每1 平衡 生物钟 激素 医学
作者
Hannah M. Costello,Sophia A. Eikenberry,Kit‐Yan Cheng,Barry J. Broderick,Advay S Joshi,Graham Scott,Annalisse Mckee,Victor M. Mendez,Lauren G. Douma,G. Ryan Crislip,Michelle L. Gumz
出处
期刊:American Journal of Physiology-renal Physiology [American Physiological Society]
标识
DOI:10.1152/ajprenal.00177.2024
摘要

Brain and muscle ARNT-Like 1 (BMAL1) is a circadian clock transcription factor that regulates physiological functions. Male adrenal-specific Bmal1 ( AS Cre/+ ::Bmal1) KO mice displayed blunted serum corticosterone rhythms, altered blood pressure rhythm, and altered timing of eating, but there is a lack of knowledge in females. This study investigates the role of adrenal BMAL1 in renal electrolyte handling and urinary aldosterone levels in response to low salt in male and female mice. Mice were placed in metabolic cages to measure 12-hour urinary aldosterone after a standard diet and 7 days low salt diet, as well as daily body weight, 12-hour food and water intake, and renal sodium and potassium balance. Adrenal glands and kidneys were collected at ZT0 or ZT12 to measure expression of aldosterone synthesis genes and clock genes. Compared to littermate controls, AS Cre/+ ::Bmal1 KO male and female mice displayed increased urinary aldosterone in response to a low salt diet, although mRNA expression of aldosterone synthesis genes was decreased. Timing of food intake was altered in AS Cre/+ ::Bmal1 KO male and female mice, with a blunted night/day ratio. AS Cre/+ ::Bmal1 KO female mice displayed decreases in renal sodium excretion in response to low salt, but both male and female KO mice had changes in sodium balance that were time-of-day-dependent. In addition, sex differences were found in adrenal and kidney clock gene expression. Notably, this study highlights sex differences in clock gene expression that could contribute to sex differences in physiological functions.

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