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憩室病中的血清素信号传导

Serotonin signaling in diverticular disease.

作者信息

Costedio Meagan M, Coates Matthew D, Danielson Amy B, Buttolph Thomas R, Blaszyk Hagen J, Mawe Gary M, Hyman Neil H

机构信息

Department of Surgery, University of Vermont College of Medicine, Burlington, VT 05405, USA.

出版信息

J Gastrointest Surg. 2008 Aug;12(8):1439-45. doi: 10.1007/s11605-008-0536-5. Epub 2008 May 20.

Abstract

Diverticulosis is extremely common in Western societies and is associated with complications in up to 15%of cases. Altered motility is an important feature of the pathogenesis of diverticular disease, and serotonin (5-HT) release is a primary trigger of gut motility. This study aims to determine whether colonic 5-HT signaling is altered in patients with diverticulosis or diverticulitis, and whether differences in serotonin signaling may distinguish patients with asymptomatic diverticulosis from those who develop disease specific complications. Sigmoid colon biopsies were obtained from healthy control subjects, individuals with asymptomatic diverticulosis, and those with a history of CT-proven diverticulitis within the preceding 6 months. The key elements of 5-HT signaling including content, release, and 5-HT transporter (SERT) expression were analyzed. A significant decrease in SERT transcript levels was present in the mucosa of patients with a history of diverticulitis when compared with controls, but not in those with asymptomatic diverticulosis. Mucosal 5-HT content, enterochromaffin (EC) cell numbers, and TpH-1 mRNA levels were comparable amongst the groups, as were basal and stimulated 5-HT release. Alterations in 5-HT signaling do not appear to be responsible for the development of diverticula. However, patients with a recent history of acute diverticulitis have a significant attenuation in SERT expression and function, likely secondary to previous inflammation. Our findings may explain the persistent symptoms of pain and altered motility so often observed in patients with diverticulitis long after recovery from the acute inflammatory response.

摘要

憩室病在西方社会极为常见,高达15%的病例会出现并发症。动力改变是憩室病发病机制的一个重要特征,而血清素(5-羟色胺,5-HT)释放是肠道动力的主要触发因素。本研究旨在确定憩室病或憩室炎患者的结肠5-HT信号是否改变,以及血清素信号的差异是否可将无症状憩室病患者与发生疾病特异性并发症的患者区分开来。从健康对照者、无症状憩室病个体以及在过去6个月内有CT证实的憩室炎病史的患者中获取乙状结肠活检样本。分析了5-HT信号的关键要素,包括含量、释放和5-HT转运体(SERT)表达。与对照组相比,有憩室炎病史患者的黏膜中SERT转录水平显著降低,但无症状憩室病患者则无此现象。各组间黏膜5-HT含量、肠嗜铬(EC)细胞数量以及TpH-1 mRNA水平相当,基础和刺激后的5-HT释放情况也相似。5-HT信号改变似乎并非憩室形成的原因。然而,近期有急性憩室炎病史的患者SERT表达和功能显著减弱,可能继发于先前的炎症。我们的研究结果或许可以解释憩室炎患者在急性炎症反应恢复后很长时间仍经常出现的持续疼痛和动力改变症状。

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