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新生儿母婴分离后成年期应激增强肾上腺素能信号促进内脏敏感性。

Neonatal Maternal Deprivation Followed by Adult Stress Enhances Adrenergic Signaling to Advance Visceral Hypersensitivity.

机构信息

Laboratory for Translational Pain Medicine, Institute of Neuroscience, Soochow University, Suzhou, 215123, China.

Center for Translational Medicine, The Zhangjiagang Affiliated Hospital of Soochow University, Zhangjiagang, 215600, China.

出版信息

Neurosci Bull. 2019 Feb;35(1):4-14. doi: 10.1007/s12264-018-0318-3. Epub 2018 Dec 17.

Abstract

The pathophysiology of visceral pain in patients with irritable bowel syndrome remains largely unknown. Our previous study showed that neonatal maternal deprivation (NMD) does not induce visceral hypersensitivity at the age of 6 weeks in rats. The aim of this study was to determine whether NMD followed by adult stress at the age of 6 weeks induces visceral pain in rats and to investigate the roles of adrenergic signaling in visceral pain. Here we showed that NMD rats exhibited visceral hypersensitivity 6 h and 24 h after the termination of adult multiple stressors (AMSs). The plasma level of norepinephrine was significantly increased in NMD rats after AMSs. Whole-cell patch-clamp recording showed that the excitability of dorsal root ganglion (DRG) neurons from NMD rats with AMSs was remarkably increased. The expression of β adrenergic receptors at the protein and mRNA levels was markedly higher in NMD rats with AMSs than in rats with NMD alone. Inhibition of β adrenergic receptors with propranolol or butoxamine enhanced the colorectal distention threshold and application of butoxamine also reversed the enhanced hypersensitivity of DRG neurons. Overall, our data demonstrate that AMS induces visceral hypersensitivity in NMD rats, in part due to enhanced NE-β adrenergic signaling in DRGs.

摘要

肠易激综合征患者内脏疼痛的病理生理学在很大程度上尚不清楚。我们之前的研究表明,新生期母鼠剥夺(NMD)不会在 6 周龄大鼠中引起内脏高敏感。本研究旨在确定 NMD 后再在 6 周龄时给予成年应激是否会诱导大鼠内脏疼痛,并探讨肾上腺素能信号在内脏疼痛中的作用。在此我们发现,NMD 大鼠在接受多次成年应激(AMSs)后 6 小时和 24 小时表现出内脏高敏感。AMSs 后 NMD 大鼠的血浆去甲肾上腺素水平显著升高。全细胞膜片钳记录显示,来自 AMSs 的 NMD 大鼠的背根神经节(DRG)神经元兴奋性显著增加。与仅接受 NMD 的大鼠相比,接受 AMSs 的 NMD 大鼠的β肾上腺素能受体在蛋白和 mRNA 水平上的表达明显更高。用普萘洛尔或丁氧胺抑制β肾上腺素能受体可增强结肠扩张阈值,并且丁氧胺的应用也可逆转 DRG 神经元的增强敏感性。总体而言,我们的数据表明,AMS 会引起 NMD 大鼠的内脏高敏感,部分原因是 DRG 中增强的 NE-β 肾上腺素能信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbe/6357269/c32dbe20f7d0/12264_2018_318_Fig1_HTML.jpg

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