Adrenal-Specific KO of the Circadian Clock Protein BMAL1 Alters Blood Pressure Rhythm and Timing of Eating Behavior

Author:

Costello Hannah M123,Crislip G Ryan123,Cheng Kit-Yan12,Lynch I Jeanette24,Juffre Alexandria125,Bratanatawira Phillip2,Mckee Annalisse1,Thelwell Ryanne S1,Mendez Victor M1,Wingo Charles S24,Douma Lauren G123,Gumz Michelle L12345ORCID

Affiliation:

1. Department of Physiology and Aging, University of Florida , Gainesville, FL 32610 , USA

2. Department of Medicine, Division of Nephrology, Hypertension, and Renal Transplantation, University of Florida , Gainesville, FL 32610 , USA

3. Center for Integrative Cardiovascular and Metabolic Diseases, University of Florida , Gainesville, FL 32610 , USA

4. Research, North Florida/South Georgia Malcolm Randall Veterans Affairs Medical Center , Gainesville, FL 32608 , USA

5. Department of Biochemistry and Molecular Biology, University of Florida , Gainesville, FL 32610 , USA

Abstract

Abstract Brain and muscle ARNT-like 1 (BMAL1) is a core circadian clock protein and transcription factor that regulates many physiological functions, including blood pressure (BP). Male global Bmal1 knockout (KO) mice exhibit ∼10 mmHg reduction in BP, as well as a blunting of BP rhythm. The mechanisms of how BMAL1 regulates BP remains unclear. The adrenal gland synthesizes hormones, including glucocorticoids and mineralocorticoids, that influence BP rhythm. To determine the role of adrenal BMAL1 on BP regulation, adrenal-specific Bmal1 (ASCre/+::Bmal1) KO mice were generated using aldosterone synthase Cre recombinase to KO Bmal1 in the adrenal gland zona glomerulosa. We confirmed the localization and efficacy of the KO of BMAL1 to the zona glomerulosa. Male ASCre/+::Bmal1 KO mice displayed a shortened BP and activity period/circadian cycle (typically 24 h) by ∼1 h and delayed peak of BP and activity by ∼2 and 3 h, respectively, compared with littermate Cre- control mice. This difference was only evident when KO mice were in metabolic cages, which acted as a stressor, as serum corticosterone was increased in metabolic cages compared with home cages. ASCre/+::Bmal1 KO mice also displayed altered diurnal variation in serum corticosterone. Furthermore, these mice have altered eating behaviors where they have a blunted night/day ratio of food intake, but no change in overall food consumed compared with controls. Overall, these data suggest that adrenal BMAL1 has a role in the regulation of BP rhythm and eating behaviors.

Funder

American Heart Association

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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