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水通道蛋白 3 和 8 在三硝基苯磺酸诱导的大鼠结肠炎中下调。

Aquaporin 3 and 8 are down-regulated in TNBS-induced rat colitis.

机构信息

Department of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai, China.

Department of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Biochem Biophys Res Commun. 2014 Jan 3;443(1):161-6. doi: 10.1016/j.bbrc.2013.11.067. Epub 2013 Nov 25.

DOI:10.1016/j.bbrc.2013.11.067
PMID:24286754
Abstract

Aquaporins (AQPs) plays an important role in transcellular water movement, but the AQPs expression profile has not been demonstrated in 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis which closely mimics human Crohn's disease (CD) histopathologically. To solve the problem, 30 female Sprague-Dawley (SD) rats were randomly divided into a model group (n=18), an ethanol control group (n=6) and a normal control group (n=6). On day 1, the rats in the model group received TNBS+50% ethanol via the rectum, while the ethanol control rats received an equal volume of 50% ethanol and the normal control rats did not receive any treatment. All rats were sacrificed on day 7, and ileum, proximal colon and distal colon specimens were obtained to examine the alteration in AQP3 and AQP8 using real-time polymerase chain reaction, Western blot analysis and immunohistochemistry. As a result, exposure to TNBS+ethanol resulted in a marked decrease in both the mRNA and protein expression of AQP3 and AQP8, with the exception of AQP8 protein which was negative in the distal colon in all three groups. These reductions in AQP3 and AQP8 were accompanied by an increase in intestinal inflammation and injury. The results obtained here implied that both AQP3 and AQP8 may be involved in the pathogenesis of inflammatory bowel disease.

摘要

水通道蛋白(AQP)在细胞间水运动中发挥重要作用,但在 2,4,6-三硝基苯磺酸(TNBS)诱导的结肠炎中,AQP 的表达谱尚未得到证实,该结肠炎在组织病理学上与人类克罗恩病(CD)非常相似。为了解决这个问题,将 30 只雌性 Sprague-Dawley(SD)大鼠随机分为模型组(n=18)、乙醇对照组(n=6)和正常对照组(n=6)。在第 1 天,模型组大鼠经直肠给予 TNBS+50%乙醇,乙醇对照组大鼠给予等体积的 50%乙醇,正常对照组大鼠不给予任何处理。所有大鼠于第 7 天处死,取回肠、近端结肠和远端结肠标本,采用实时聚合酶链反应、Western blot 分析和免疫组织化学方法检测 AQP3 和 AQP8 的变化。结果显示,暴露于 TNBS+乙醇会导致 AQP3 和 AQP8 的 mRNA 和蛋白表达明显降低,但在所有三组中,AQP8 蛋白在远端结肠均为阴性。AQP3 和 AQP8 的减少伴随着肠道炎症和损伤的增加。这里的结果表明,AQP3 和 AQP8 可能都参与了炎症性肠病的发病机制。

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