内脏脂肪交感神经切除术可改善与慢性睡眠限制有关的全身和局部应激反应。

IF 2.8 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Experimental Biology and Medicine Pub Date : 2023-12-01 Epub Date: 2023-12-25 DOI:10.1177/15353702231214267
Lucia E Azuara-Alvarez, Mauricio Díaz-Muñoz, Adrián Báez Ruiz, Nadia Saderi, Oscar Daniel Ramírez-Plascencia, Skarleth Cárdenas-Romero, Omar Flores-Sandoval, Roberto Salgado-Delgado
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引用次数: 0

摘要

睡眠平衡失调会引发各种健康问题,包括肥胖、糖尿病等新陈代谢紊乱和压力增加。睡眠和压力双向作用,影响中枢神经系统和新陈代谢。小鼠模型表明,睡眠时间的减少与系统应激反应的增加有关,其特点是内分泌失调,包括下丘脑-垂体-肾上腺轴活动增加、胰岛素增加和脂肪连素减少,从而影响外周器官的生理机能,主要是白色脂肪组织(WAT)。在外周器官内,局部应激反应也会通过促进皮质酮的形成而被激活。这种局部放大的糖皮质激素信号传导是通过激活 11β- 羟类固醇脱氢酶 1 型(11β-HSD1)来实现的。在脂肪中,交感神经系统会上调 11β-HSD1 的活性,这表明睡眠不足、应激反应增强和潜在的脂肪代谢紊乱之间存在联系。为了进一步了解这种关系,我们分析了切除 WAT 的大鼠的代谢和应激反应,以确定在慢性睡眠限制期间,自律神经系统对应激反应相关代谢紊乱的贡献。在为期八周的时间里,雄性 Wistar 大鼠每天只能睡 6 小时。结果显示,限制睡眠的大鼠血清皮质酮升高,脂肪组织 11β-HSD1 活性增加,体重下降,内脏脂肪减少,脂肪连素增加,瘦素水平降低,葡萄糖耐量受损,每日体温轻度下降。相反,限制睡眠的交感神经切除大鼠则表现出应激反应减弱(血清皮质酮和 11β-HSD1 活性降低)。此外,内脏脂肪垫、瘦素和脂肪连素减少,葡萄糖管理得到改善,体温持续下降,这些都说明交感神经切除的大鼠保持了体重减轻。这些结果表明,自律神经系统在一定程度上导致了 WAT 加剧的应激反应及其代谢和生理紊乱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visceral fat sympathectomy ameliorates systemic and local stress response related to chronic sleep restriction.

Disturbance of sleep homeostasis encompasses health issues, including metabolic disorders like obesity, diabetes, and augmented stress vulnerability. Sleep and stress interact bidirectionally to influence the central nervous system and metabolism. Murine models demonstrate that decreased sleep time is associated with an increased systemic stress response, characterized by endocrinal imbalance, including the elevated activity of hypothalamic-pituitary-adrenal axis, augmented insulin, and reduced adiponectin, affecting peripheral organs physiology, mainly the white adipose tissue (WAT). Within peripheral organs, a local stress response can also be activated by promoting the formation of corticosterone. This local amplifying glucocorticoid signaling is favored through the activation of the enzyme 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1). In WAT, 11β-HSD1 activity is upregulated by the sympathetic nervous system, suggesting a link between sleep loss, augmented stress response, and a potential WAT metabolic disturbance. To gain more understanding about this relationship, metabolic and stress responses of WAT-sympathectomized rats were analyzed to identify the contribution of the autonomic nervous system to stress response-related metabolic disorders during chronic sleep restriction. Male Wistar rats under sleep restriction were allowed just 6 h of daily sleep over eight weeks. Results showed that rats under sleep restriction presented higher serum corticosterone, increased adipose tissue 11β-HSD1 activity, weight loss, decreased visceral fat, augmented adiponectin, lower leptin levels, glucose tolerance impairment, and mildly decreased daily body temperature. In contrast, sympathectomized rats under sleep restriction exhibited decreased stress response (lower serum corticosterone and 11β-HSD1 activity). In addition, they maintained weight loss, explained by a reduced visceral fat pad, leptin, and adiponectin, improved glucose management, and persisting decline in body temperature. These results suggest autonomic nervous system is partially responsible for the WAT-exacerbated stress response and its metabolic and physiological disturbances.

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来源期刊
Experimental Biology and Medicine
Experimental Biology and Medicine 医学-医学:研究与实验
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
1 months
期刊介绍: Experimental Biology and Medicine (EBM) is a global, peer-reviewed journal dedicated to the publication of multidisciplinary and interdisciplinary research in the biomedical sciences. EBM provides both research and review articles as well as meeting symposia and brief communications. Articles in EBM represent cutting edge research at the overlapping junctions of the biological, physical and engineering sciences that impact upon the health and welfare of the world''s population. Topics covered in EBM include: Anatomy/Pathology; Biochemistry and Molecular Biology; Bioimaging; Biomedical Engineering; Bionanoscience; Cell and Developmental Biology; Endocrinology and Nutrition; Environmental Health/Biomarkers/Precision Medicine; Genomics, Proteomics, and Bioinformatics; Immunology/Microbiology/Virology; Mechanisms of Aging; Neuroscience; Pharmacology and Toxicology; Physiology; Stem Cell Biology; Structural Biology; Systems Biology and Microphysiological Systems; and Translational Research.
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