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Dysbiosis of gut microbiota contributes to chronic stress in endometriosis patients via activating inflammatory pathway

机译:肠道菌群失调通过激活炎症途径促进子宫内膜异位症患者的慢性应激

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Background: Gut microbiota can interact with the central nervous system through the gut–brain axis, thus affecting the host's chronic stress level, such as anxiety and depression. Current researches show that patients with endometriosis often have a high level of chronic stress, which will in turn aggravate endometriosis by activating the β-adrenergic signaling pathway. Therefore, we wondered whether the gut microbiota associates with the chronic stress level in endometriosis patients, which may provide new insights on how to improve treatment. Methods: We grouped the endometriosis patients into the chronic stress group and the control group with questionnaires such as generalized anxiety disorder-7 and patient health questionnaire-9 and collected patients' fecal specimens and tissue specimens. Gut microbiota compositions were analyzed by the 16SrRNA gene sequencing-based method, and immunohistochemistry was performed to detect the activation of inflammatory pathways in endometriosis tissues. Results: We found that in patients with endometriosis, the dysbiosis of gut microbiota was associated with their stress levels. Furthermore, the levels of Paraprevotella, Odoribacter, Veillonella, and Ruminococcus were significantly reduced in chronic stressed endometriosis patients, suggestive of a disease-specific change of gut microbiota at the genus level. Compared to the healthy women, the expression levels of inflammatory cytokines, nuclear factor-κB p65, and cyclooxygenase-2 increased in the chronic stressed endometriosis patients, indicating that the dysbiosis of gut microbiota may activate the inflammatory pathway of gut–brain axis. Conclusions: We hypothesized that these new disease-specific changes of gut microbiota in chronic stressed patients with endometriosis may be a new examination target of chronic stress level. These changes may also provide new insights for psychological intervention, thus reducing the stress level and improving the prognosis of endometriosis patients.
机译:背景:肠道菌群可通过肠脑轴与中枢神经系统相互作用,从而影响宿主的慢性应激水平,如焦虑和抑郁。当前的研究表明,子宫内膜异位症患者通常具有较高的慢性应激水平,这反过来会通过激活β-肾上腺素能信号传导通路加重子宫内膜异位症。因此,我们想知道肠道菌群是否与子宫内膜异位症患者的慢性应激水平有关,这可能为如何改善治疗提供新的见解。方法:我们将子宫内膜异位症患者分为慢性应激组和对照组,分别采用问卷调查(如广泛性焦虑障碍7和患者健康调查表9),并收集患者的粪便样本和组织样本。通过基于16SrRNA基因测序的方法分析肠道菌群的组成,并进行免疫组织化学检测子宫内膜异位症组织中炎症途径的激活。结果:我们发现,在子宫内膜异位症患者中,肠道菌群的营养不良与其压力水平有关。此外,在慢性应激的子宫内膜异位症患者中,副preparvotella,Odoribacter,Veillonella和Ruminococcus的水平显着降低,提示该属水平的肠道菌群有疾病特异性的变化。与健康女性相比,慢性应激性子宫内膜异位症患者中炎性细胞因子,核因子-κBp65和环氧合酶-2的表达水平增加,表明肠道菌群失调可能激活了肠-脑轴的炎症途径。结论:我们假设,慢性应激子宫内膜异位症患者肠道微生物群的这些新的疾病特异性变化可能是慢性应激水平的新检查目标。这些变化也可能为心理干预提供新的见解,从而降低压力水平并改善子宫内膜异位症患者的预后。

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