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本文引用的文献

1
Identification of the visceral pain pathway activated by noxious colorectal distension in mice.鉴定小鼠中由结直肠扩张诱发的内脏痛觉通路。
Front Neurosci. 2011 Feb 22;5:16. doi: 10.3389/fnins.2011.00016. eCollection 2011.
2
Characterization of silent afferents in the pelvic and splanchnic innervations of the mouse colorectum.对小鼠直肠盆腔和内脏传入神经中沉默传入纤维的特性研究。
Am J Physiol Gastrointest Liver Physiol. 2011 Jan;300(1):G170-80. doi: 10.1152/ajpgi.00406.2010. Epub 2010 Nov 11.
3
Interactions between the immune and nervous systems in pain.免疫系统与神经系统在疼痛中的相互作用。
Nat Med. 2010 Nov;16(11):1267-76. doi: 10.1038/nm.2234. Epub 2010 Oct 14.
4
Calcium-activated pathways and oxidative burst mediate zymosan-induced signaling and IL-10 production in human macrophages.钙激活途径和氧化爆发介导酵母聚糖诱导的人巨噬细胞信号转导和 IL-10 产生。
J Immunol. 2010 May 15;184(10):5545-52. doi: 10.4049/jimmunol.0901293. Epub 2010 Apr 16.
5
Pathogenesis of IBS: role of inflammation, immunity and neuroimmune interactions.IBS 的发病机制:炎症、免疫和神经免疫相互作用的作用。
Nat Rev Gastroenterol Hepatol. 2010 Mar;7(3):163-73. doi: 10.1038/nrgastro.2010.4. Epub 2010 Jan 26.
6
Differential roles of stretch-sensitive pelvic nerve afferents innervating mouse distal colon and rectum.拉伸敏感的支配小鼠远端结肠和直肠的盆神经传入纤维的差异作用。
Am J Physiol Gastrointest Liver Physiol. 2010 Mar;298(3):G402-9. doi: 10.1152/ajpgi.00487.2009. Epub 2010 Jan 14.
7
Elevated pro-inflammatory and lipotoxic mucosal lipids characterise irritable bowel syndrome.升高的促炎和脂毒性黏膜脂质特征性地存在于肠易激综合征中。
World J Gastroenterol. 2009 Dec 28;15(48):6068-74. doi: 10.3748/wjg.15.6068.
8
Cytokine and chemokine regulation of sensory neuron function.细胞因子和趋化因子对感觉神经元功能的调节
Handb Exp Pharmacol. 2009(194):417-49. doi: 10.1007/978-3-540-79090-7_12.
9
Visceral pain: the neurophysiological mechanism.内脏痛:神经生理机制
Handb Exp Pharmacol. 2009(194):31-74. doi: 10.1007/978-3-540-79090-7_2.
10
Electroacupuncture attenuates visceral hyperalgesia and inhibits the enhanced excitability of colon specific sensory neurons in a rat model of irritable bowel syndrome.电针对肠易激综合征大鼠模型内脏痛觉过敏的缓解作用及对结肠特定感觉神经元兴奋性增强的抑制作用。
Neurogastroenterol Motil. 2009 Dec;21(12):1302-e125. doi: 10.1111/j.1365-2982.2009.01354.x. Epub 2009 Jun 24.

持续结直肠高敏感小鼠机械敏感和非敏感传入纤维的长期致敏。

Long-term sensitization of mechanosensitive and -insensitive afferents in mice with persistent colorectal hypersensitivity.

机构信息

Center for Pain Research, Univ. of Pittsburgh, Pittsburgh, PA 15213, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2012 Apr;302(7):G676-83. doi: 10.1152/ajpgi.00490.2011. Epub 2012 Jan 19.

DOI:10.1152/ajpgi.00490.2011
PMID:22268098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3330779/
Abstract

Afferent input contributes significantly to the pain and colorectal hypersensitivity that characterize irritable bowel syndrome. In the present study, we investigated the contributions of mechanically sensitive and mechanically insensitive afferents (MIAs; or silent afferents) to colorectal hypersensitivity. The visceromotor response to colorectal distension (CRD; 15-60 mmHg) was recorded in mice before and for weeks after intracolonic treatment with zymosan or saline. After CRD tests, the distal colorectum with the pelvic nerve attached was removed for single-fiber electrophysiological recordings. Colorectal afferent endings were located by electrical stimulation and characterized as mechanosensitive or not by blunt probing, mucosal stroking, and circumferential stretch. Intracolonic zymosan produced persistent colorectal hypersensitivity (>24 days) associated with brief colorectal inflammation. Pelvic nerve muscular-mucosal but not muscular mechanosensitive afferents recorded from mice with colorectal hypersensitivity exhibited persistent sensitization. In addition, the proportion of MIAs (relative to control) was significantly reduced from 27% to 13%, whereas the proportion of serosal afferents was significantly increased from 34% to 53%, suggesting that MIAs acquired mechanosensitivity. PGP9.5 immunostaining revealed no significant loss of colorectal nerve fiber density, suggesting that the reduction in MIAs is not due to peripheral fiber loss after intracolonic zymosan. These results indicate that colorectal MIAs and sensitized muscular-mucosal afferents that respond to stretch contribute significantly to the afferent input that sustains hypersensitivity to CRD, suggesting that targeted management of colorectal afferent input could significantly reduce patients' complaints of pain and hypersensitivity.

摘要

传入输入对功能性肠病的疼痛和结肠高敏性有重要贡献。在本研究中,我们研究了机械敏感传入和机械不敏感传入(MIA;或沉默传入)对结肠高敏性的贡献。在给予酵母聚糖或盐水的腔内治疗前和治疗后数周,记录了小鼠对结肠扩张(CRD;15-60mmHg)的内脏运动反应。在 CRD 测试后,去除带有盆神经的远端结肠进行单纤维电生理记录。通过电刺激定位结肠传入末梢,并通过钝探针探查、黏膜刷擦和环周拉伸将其特征化为机械敏感或不敏感。腔内酵母聚糖产生持续的结肠高敏性(>24 天),伴有短暂的结肠炎症。从有结肠高敏性的小鼠中记录到的盆神经肌肉-黏膜但非肌肉机械敏感传入持续敏感。此外,MIA 的比例(相对于对照)从 27%显著降低到 13%,而浆膜传入的比例从 34%显著增加到 53%,表明 MIA 获得了机械敏感性。PGP9.5 免疫染色显示结肠神经纤维密度无明显减少,表明腔内酵母聚糖后 MIA 的减少不是由于周围纤维丢失。这些结果表明,结肠 MIA 和对拉伸有反应的致敏肌肉-黏膜传入对维持 CRD 高敏性的传入输入有重要贡献,提示靶向管理结肠传入输入可能会显著减轻患者对疼痛和高敏性的抱怨。