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Infralimbic cortical glutamate output is necessary for the neural and behavioral consequences of chronic stress.边缘下皮质谷氨酸输出对于慢性应激的神经和行为后果是必要的。
Neurobiol Stress. 2020 Nov 23;13:100274. doi: 10.1016/j.ynstr.2020.100274. eCollection 2020 Nov.
2
Peripheral Innervation in the Regulation of Glucose Homeostasis.外周神经在血糖稳态调节中的作用。
Trends Neurosci. 2021 Mar;44(3):189-202. doi: 10.1016/j.tins.2020.10.015. Epub 2020 Nov 20.
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Prefrontal Cortex Regulates Chronic Stress-Induced Cardiovascular Susceptibility.前额皮质调节慢性应激诱导的心血管易感性。
J Am Heart Assoc. 2019 Dec 17;8(24):e014451. doi: 10.1161/JAHA.119.014451. Epub 2019 Dec 14.
4
Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats.慢性青少年期应激和糖皮质激素受体选择性调节对雄性和雌性大鼠的持久影响。
Psychoneuroendocrinology. 2020 Feb;112:104490. doi: 10.1016/j.psyneuen.2019.104490. Epub 2019 Oct 27.
5
Glucocorticoids regulate adipose tissue protein concentration in a depot- and sex-specific manner.糖皮质激素以 depot 和性别特异性的方式调节脂肪组织蛋白浓度。
Stress. 2020 Mar;23(2):243-247. doi: 10.1080/10253890.2019.1658736. Epub 2019 Sep 10.
6
Sex Differences in Vulnerability and Resilience to Stress Across the Life Span.性别在整个生命周期中的压力脆弱性和弹性差异。
Biol Psychiatry. 2019 Sep 15;86(6):421-432. doi: 10.1016/j.biopsych.2019.04.028. Epub 2019 May 7.
7
Effects of combined glucocorticoid/mineralocorticoid receptor modulation (CORT118335) on energy balance, adiposity, and lipid metabolism in male rats.联合糖皮质激素/盐皮质激素受体调节(CORT118335)对雄性大鼠能量平衡、肥胖和脂代谢的影响。
Am J Physiol Endocrinol Metab. 2019 Aug 1;317(2):E337-E349. doi: 10.1152/ajpendo.00018.2019. Epub 2019 May 21.
8
Coping with the forced swim stressor: Current state-of-the-art.应对强迫游泳应激源:最新进展。
Behav Brain Res. 2019 May 17;364:1-10. doi: 10.1016/j.bbr.2019.02.005. Epub 2019 Feb 6.
9
Associations between symptoms of depression and anxiety and cortisol responses to and recovery from acute stress.抑郁和焦虑症状与急性应激的皮质醇反应和恢复之间的关联。
Psychoneuroendocrinology. 2019 Apr;102:44-52. doi: 10.1016/j.psyneuen.2018.11.035. Epub 2018 Nov 24.
10
Measuring corticosterone concentrations over a physiological dynamic range in female rats.测量雌性大鼠生理动态范围内的皮质酮浓度。
Physiol Behav. 2018 Oct 1;194:73-76. doi: 10.1016/j.physbeh.2018.04.033. Epub 2018 May 3.

大鼠慢性应激后糖调节和应对行为:跨生命周期的性别差异。

Glucoregulation and coping behavior after chronic stress in rats: Sex differences across the lifespan.

机构信息

Biomedical Sciences, Colorado State University, Fort Collins, CO, United States of America.

Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, United States of America.

出版信息

Horm Behav. 2021 Nov;136:105060. doi: 10.1016/j.yhbeh.2021.105060. Epub 2021 Sep 16.

DOI:10.1016/j.yhbeh.2021.105060
PMID:34537487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8629951/
Abstract

The purpose of the current study was to determine how biological sex shapes behavioral coping and metabolic health across the lifespan after chronic stress. We hypothesized that examining chronic stress-induced behavioral and endocrine outcomes would reveal sex differences in the biological basis of susceptibility. During late adolescence, male and female Sprague-Dawley rats experienced chronic variable stress (CVS). Following completion of CVS, all rats experienced a forced swim test (FST) followed 3 days later by a fasted glucose tolerance test (GTT). The FST was used to determine coping in response to a stressor. Endocrine metabolic function was evaluated in the GTT by measuring glucose and corticosterone, the primary rodent glucocorticoid. Rats then aged to 15 months when the FST and GTT were repeated. In young rats, chronically stressed females exhibited more passive coping and corticosterone release in the FST. Additionally, chronically stressed females had elevated corticosterone and impaired glucose clearance in the GTT. Aging affected all measurements as behavioral and endocrine outcomes were sex specific. Furthermore, regression analysis between hormonal and behavioral responses identified associations depending on sex and stress. Collectively, these data indicate increased female susceptibility to the effects of chronic stress during adolescence. Further, translational investigation of coping style and glucose homeostasis may identify biomarkers for stress-related disorders.

摘要

本研究旨在确定生物性别如何影响慢性应激后整个生命周期的行为应对和代谢健康。我们假设,检查慢性应激诱导的行为和内分泌结果将揭示易感性的生物学基础中的性别差异。在青春期后期,雄性和雌性 Sprague-Dawley 大鼠经历慢性可变应激 (CVS)。完成 CVS 后,所有大鼠都进行了强迫游泳测试 (FST),3 天后进行了空腹葡萄糖耐量测试 (GTT)。FST 用于确定对压力源的应对。GTT 通过测量葡萄糖和皮质酮(主要的啮齿动物糖皮质激素)来评估内分泌代谢功能。然后,大鼠长到 15 个月大时,再次进行 FST 和 GTT。在年轻大鼠中,慢性应激的雌性大鼠在 FST 中表现出更多的被动应对和皮质酮释放。此外,慢性应激的雌性大鼠皮质酮升高,葡萄糖清除受损。衰老影响所有测量值,因为行为和内分泌结果具有性别特异性。此外,激素和行为反应之间的回归分析根据性别和应激确定了关联。总的来说,这些数据表明青春期女性对慢性应激影响的易感性增加。此外,对应对方式和葡萄糖稳态的转化研究可能会确定与应激相关的疾病的生物标志物。