外侧导水管周围灰质参与慢性约束应激诱导肠易激综合征的调节。

IF 5.1 2区 医学 Q1 NEUROSCIENCES Neurobiology of Disease Pub Date : 2025-01-01 DOI:10.1016/j.nbd.2024.106758
Jiaotao Xing , Ying Li , Jiali Hu , Liyao Gu , Guanghua Sun , Xiangle Li
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引用次数: 0

摘要

肠易激综合征(IBS)是一种功能性肠道疾病,其特征是反复腹痛,并伴有排便习惯不规则和大便频率及稠度的改变。目前,IBS被认为是一种肠-脑相互作用的疾病,越来越多的研究集中在脑-肠轴上。然而,与肠易激综合征相关的大脑区域尚未得到充分研究。在本研究中,我们利用慢性约束应激(CRS)模型在小鼠中引起ibs样症状,并伴有焦虑样行为和痛觉过敏。通过cFOS染色,我们观察到CRS后小鼠侧导水管周围灰质(LPAG)的活化。通过破伤风毒素或化学遗传学抑制LPAG的活性,我们发现LPAG的化学遗传学激活可引起ibs样症状,而LPAG的化学遗传学激活可引起ibs样症状。最后,我们使用经典镇痛药物舒芬太尼,发现它可以缓解crs诱导的ibs样症状。
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Lateral periaqueductal gray participate in the regulation of irritable bowel syndrome induced by chronic restraint stress
Irritable bowel syndrome (IBS) is a functional bowel disorder defined by recurrent abdominal pain, coupled with irregular bowel habits and alterations in the frequency as well as the consistency of stool. At present, IBS is considered as a disease of gut-brain interaction, and an increasing number of studies are focusing on the brain-gut axis. However, the brain regions associated with IBS have not been fully studied yet. In this study, we utilized the chronic restraint stress (CRS) model to evoke IBS-like symptoms in mice, which were accompanied by anxiety-like behaviors and hyperalgesia. Through cFOS staining, we observed the activation of the lateral periaqueductal gray (LPAG) in the mice after CRS. By inhibiting the activity of the LPAG through tetanus toxin or chemogenetics, we found that IBS-like symptoms could be relieved, whereas chemogenetic activation of the LPAG induced IBS-like symptoms. Finally, we utilized the classic analgesic drug sufentanil and found that it could alleviate CRS-induced IBS-like symptoms.
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来源期刊
Neurobiology of Disease
Neurobiology of Disease 医学-神经科学
CiteScore
11.20
自引率
3.30%
发文量
270
审稿时长
76 days
期刊介绍: Neurobiology of Disease is a major international journal at the interface between basic and clinical neuroscience. The journal provides a forum for the publication of top quality research papers on: molecular and cellular definitions of disease mechanisms, the neural systems and underpinning behavioral disorders, the genetics of inherited neurological and psychiatric diseases, nervous system aging, and findings relevant to the development of new therapies.
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