College of Veterinary Medicine, China Agricultural University, Beijing 100193, P.R. China.
Department of Horticulture and Landscape Architecture, Jiangsu Agri-animal Husbandry Vocational College, Taizhou 225300, P.R. China.
Int J Biol Sci. 2024 Aug 19;20(11):4476-4495. doi: 10.7150/ijbs.97275. eCollection 2024.
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 demonstrated that 5-HT impairs mitochondrial biogenesis by inhibiting the AMPK-PGC-1α axis via 5-HT receptors and the cAMP-PKA pathway. Pharmacological inhibition of serotonin synthesis or 5-HT 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.
慢性应激与胃肠道疾病密切相关。然而,应激相关神经递质如 5-羟色胺(5-hydroxytryptamine,5-HT)在慢性应激条件下对肠道的影响仍知之甚少。本研究旨在阐明 5-HT 在慢性应激期间影响线粒体生物发生和肠道屏障完整性的机制。我们采用慢性束缚应激(CRS)小鼠模型,观察到肠道 5-HT 水平升高,结肠黏膜结构改变,紧密连接破坏。5-HT 的增加与血清素合成酶上调和 5-HT 再摄取转运体下调有关,表明慢性应激引起的 5-HT 稳态失衡。此外,5-HT 加剧了氧化应激和紧密连接蛋白表达的损伤,突出了其促进肠道屏障功能障碍的作用。细胞实验表明,5-HT 通过 5-HT 受体和 cAMP-PKA 途径抑制 AMPK-PGC-1α 轴,从而损害线粒体生物发生。5-HT 合成或 5-HT 受体的药理学抑制减轻了 5-HT 和慢性应激引起的肠道屏障损伤,恢复了线粒体生物发生。这些发现提供了有力的证据,表明 5-HT 通过抑制 AMPK-PGC-1α 轴加剧慢性应激诱导的肠道屏障破坏,为针对 5-HT 对肠道的有害影响的新型治疗干预措施铺平了道路,特别是在慢性应激条件下。