Estrogen signaling is necessary for the sex difference in simulated jet lag in mice.

IF 3.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Maria A Venegas, Nicholas Westray, Samuel Nwadialo, Yuriko Katsumata, Julie S Pendergast
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引用次数: 0

Abstract

The circadian system coordinates 24-h cycles of internal biological processes with the environmental light-dark cycle. Abrupt shifts in the timing of the light-dark cycle misalign internal circadian clocks with the environment and cause jet lag until resynchronization occurs. The objective of this study was to investigate the sex difference in simulated jet lag in mice. Female mice resynchronized faster than male mice to 6-h advances of the light-dark cycle that mimicked eastward travel. Circulating estradiol was necessary and sufficient for rapid resynchronization in female mice since ovariectomized females resynchronized slower than mice treated with estradiol. Disabling estrogen receptor α (ERα), but not estrogen receptor β (ERβ) or G-protein-coupled estrogen receptor 1 (GPER1), abolished the sex difference in resynchronization. To investigate ERα-dependent mechanisms that regulate the rate of resynchronization, we measured the endogenous circadian period and the magnitudes of phase shifts to light pulses in male and female wild-type and ERα knockout mice. Wild-type females had shorter periods and greater phase delays in response to light pulses given in the early subjective night than male mice. Disabling ERα abolished these sex differences by lengthening the circadian period and reducing the magnitudes of phase delays. Together, these data suggest that ERα alters the rate of resynchronization to shifted light-dark cycles by regulating period length and phase shift magnitude in female mice. Understanding the mechanisms underlying the sex difference in resynchronization to shifted light-dark cycles can be used to develop strategies to alleviate jet lag and circadian misalignment.NEW & NOTEWORTHY Coordination of circadian rhythms with environmental cycles of light and dark is critical to well-being and healthspan. Jet lag is circadian misalignment that causes fatigue, insomnia, poor mood, impaired alertness, and gastrointestinal symptoms after travel across time zones. We show there is a sex difference in simulated jet lag in mice that is regulated by ERα signaling. Our findings reveal novel mechanisms that underlie jet lag to understand and develop interventions for circadian misalignment.

雌性激素信号对于小鼠模拟时差的性别差异是必要的。
昼夜节律系统协调内部生物过程的24小时周期与环境的光暗周期。昼夜周期的突然变化使体内生物钟与环境不一致,导致时差反应,直到重新同步发生。本研究的目的是研究小鼠模拟时差的性别差异。雌性老鼠比雄性老鼠更快地将光暗周期提前6个小时,以模拟向东旅行。循环雌二醇对雌性小鼠的快速再同步是必要和充分的,因为卵巢切除的雌性小鼠的再同步速度比雌二醇处理的小鼠慢。雌激素受体α (ERα)的失活,而ERβ或g蛋白偶联雌激素受体1 (GPER1)的失活,消除了再同步的性别差异。为了研究ERα依赖的调节再同步率的机制,我们测量了雄性和雌性野生型和ERα敲除小鼠的内源性昼夜节律周期和相移到光脉冲的幅度。与雄性小鼠相比,野生型雌性小鼠对主观夜晚早期给予的光脉冲的反应周期更短,相位延迟更大。失能ERα通过延长昼夜节律周期和减少相位延迟的幅度来消除这些性别差异。综上所述,这些数据表明,ERα通过调节雌性小鼠的周期长度和相移幅度,改变了光暗周期移位的再同步率。了解在光暗周期转移的再同步过程中性别差异的潜在机制,可以用来制定缓解时差和昼夜节律失调的策略。
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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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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