Chronic Stress-induced Serotonin Impairs Intestinal Epithelial Cell Mitochondrial Biogenesis via the AMPK-PGC-1α Axis.

IF 8.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
International Journal of Biological Sciences Pub Date : 2024-08-19 eCollection Date: 2024-01-01 DOI:10.7150/ijbs.97275
Ding Yang, Yan Sun, Pei Wen, Yaoxing Chen, Jing Cao, Xuelin Sun, Yulan Dong
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引用次数: 0

Abstract

Chronic stress is closely associated with gastrointestinal disorders. However, the impact of stress-related neurotransmitters such as serotonin (5-hydroxytryptamine, 5-HT) on the intestines under chronic stress conditions remains poorly understood. This study aims to elucidate the mechanisms by which 5-HT affects mitochondrial biogenesis and intestinal barrier integrity during chronic stress. Employing a chronic restraint stress (CRS) mouse model, we observed elevated intestinal 5-HT levels, altered colonic mucosal structure, and disrupted tight junctions. The increase in 5-HT was associated with up-regulated serotonin synthesis enzymes and downregulated serotonin reuptake transporters, indicating an imbalance in serotonin homeostasis imbalance caused by chronic stress. Furthermore, serotonin exacerbated oxidative stress and impaired tight junction protein expression, highlighting its role in promoting intestinal barrier dysfunction. Experiments with cells in vitro demonstrated that 5-HT impairs mitochondrial biogenesis by inhibiting the AMPK-PGC-1α axis via 5-HT7 receptors and the cAMP-PKA pathway. Pharmacological inhibition of serotonin synthesis or 5-HT7 receptors alleviated the intestinal barrier damage caused by 5-HT and chronic stress, restoring mitochondrial biogenesis. These findings provide compelling evidence that serotonin exacerbates chronic stress-induced intestinal barrier disruption by inhibiting the AMPK-PGC-1α axis, paving the way for novel therapeutic interventions targeting the detrimental effects of serotonin on the intestine, particularly under chronic stress conditions.

慢性压力诱导的羟色胺通过 AMPK-PGC-1α 轴损害肠上皮细胞线粒体生物生成
慢性压力与胃肠功能紊乱密切相关。然而,在慢性应激条件下,应激相关神经递质(如血清素(5-羟色胺,5-HT))对肠道的影响仍鲜为人知。本研究旨在阐明 5-HT 在慢性应激过程中影响线粒体生物生成和肠道屏障完整性的机制。利用慢性束缚应激(CRS)小鼠模型,我们观察到肠道 5-HT 水平升高、结肠粘膜结构改变和紧密连接破坏。5-羟色胺的增加与血清素合成酶上调和血清素再摄取转运体下调有关,表明慢性应激导致血清素平衡失调。此外,血清素还加剧了氧化应激,损害了紧密连接蛋白的表达,突出了它在促进肠屏障功能障碍方面的作用。体外细胞实验表明,5-羟色胺通过 5-HT7 受体和 cAMP-PKA 通路抑制 AMPK-PGC-1α 轴,从而损害线粒体生物生成。药物抑制血清素合成或 5-HT7 受体可减轻 5-HT 和慢性应激对肠道屏障的损伤,恢复线粒体的生物生成。这些发现提供了令人信服的证据,证明血清素通过抑制AMPK-PGC-1α轴加剧了慢性应激诱导的肠屏障破坏,为针对血清素对肠道的有害影响(尤其是在慢性应激条件下)的新型治疗干预铺平了道路。
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
International Journal of Biological Sciences
International Journal of Biological Sciences 生物-生化与分子生物学
CiteScore
16.90
自引率
1.10%
发文量
413
审稿时长
1 months
期刊介绍: The International Journal of Biological Sciences is a peer-reviewed, open-access scientific journal published by Ivyspring International Publisher. It dedicates itself to publishing original articles, reviews, and short research communications across all domains of biological sciences.
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