肾上腺特异性 KO 昼夜节律时钟蛋白 BMAL1 会改变血压节律和进食行为的时间。

IF 5.1 Q2 CELL BIOLOGY Function (Oxford, England) Pub Date : 2023-01-09 eCollection Date: 2023-01-01 DOI:10.1093/function/zqad001
Hannah M Costello, G Ryan Crislip, Kit-Yan Cheng, I Jeanette Lynch, Alexandria Juffre, Phillip Bratanatawira, Annalisse Mckee, Ryanne S Thelwell, Victor M Mendez, Charles S Wingo, Lauren G Douma, Michelle L Gumz
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引用次数: 0

摘要

脑和肌肉 ARNT 样 1(BMAL1)是一种核心昼夜节律钟蛋白和转录因子,可调节多种生理功能,包括血压(BP)。雄性全基因 Bmal1 敲除(KO)小鼠的血压降低了 10 mmHg,血压节律也变得迟钝。BMAL1 调节血压的机制仍不清楚。肾上腺合成的激素(包括糖皮质激素和矿物质皮质激素)会影响血压节律。为了确定肾上腺 BMAL1 在血压调节中的作用,我们利用醛固酮合成酶 Cre 重组技术在肾上腺肾小球上 KO 了肾上腺特异性 Bmal1(ASCre/+ ::Bmal1 )小鼠。我们证实了 BMAL1 在肾小球肾上腺的定位和 KO 效果。与同窝 Cre- 对照组小鼠相比,雄性 ASCre/+ ::Bmal1 KO 小鼠的血压和活动期/昼夜节律周期(通常为 24 小时)缩短了 ∼ 1 小时,血压和活动的峰值分别延迟了 ∼ 2 小时和 3 小时。只有当 KO 小鼠被关在作为应激源的代谢笼中时,这种差异才会明显,因为与家庭笼相比,代谢笼中的血清皮质酮增加了。AS Cre/+ ::Bmal1 KO小鼠的血清皮质酮昼夜变化也发生了改变。此外,这些小鼠的进食行为也发生了改变,与对照组相比,它们的夜间/白天食物摄入比减弱,但总体食物摄入量没有变化。总之,这些数据表明肾上腺 BMAL1 在调节血压节律和进食行为中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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. AS Cre/+ ::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.

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