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ENaC表达改变导致克罗恩病非炎症性肠段钠吸收受损。

Altered ENaC expression leads to impaired sodium absorption in the noninflamed intestine in Crohn's disease.

作者信息

Zeissig Sebastian, Bergann Theresa, Fromm Anja, Bojarski Christian, Heller Frank, Guenther Ute, Zeitz Martin, Fromm Michael, Schulzke Jörg-Dieter

机构信息

Department of Gastroenterology, Infectious Diseases, and Rheumatology, Charité, Campus Benjamin Franklin, Berlin, Germany.

出版信息

Gastroenterology. 2008 May;134(5):1436-47. doi: 10.1053/j.gastro.2008.02.030. Epub 2008 Feb 17.

Abstract

BACKGROUND & AIMS: Crohn's disease (CD) is a chronic inflammatory bowel disease. In this study, we have investigated sodium absorption via epithelial sodium channels (ENaC) in the macroscopically noninflamed colon in active CD.

METHODS

Sodium transport via ENaC was investigated in Ussing chambers using biopsy specimens of sigmoid colon from controls and active CD limited to the small intestine. ENaC messenger RNA expression and subcellular localization were studied by real-time polymerase chain reaction and confocal microscopy. Effects of proinflammatory cytokines on ENaC and signaling via mitogen-activated protein kinases were investigated in rat distal colon. Therapeutic inhibition of mitogen-activated protein kinases was studied in CD biopsy specimens.

RESULTS

Electrogenic sodium absorption via ENaC was strongly impaired in the macroscopically noninflamed CD colon because of reduced gamma-ENaC transcription, whereas subcellular localization of ENaC was not changed. In contrast to impaired epithelial sodium transport, epithelial barrier function was not altered in noninflamed CD colon, indicating that paracellular leak flux of ions did not contribute to decreased sodium absorption. Exposure of rat distal colon to tumor necrosis factor alpha led to reduced electrogenic sodium absorption because of impaired transcriptional gamma-ENaC induction, which resembled the changes found in CD. Tumor necrosis factor alpha effects were dependent on extracellular signal-regulated kinase 1/2 but not p38 or c-Jun-N-terminal kinase because inhibition of mitogen-activated protein kinase/extracellular regulated kinase (MEK)1/2 but not inhibition of p38 or c-Jun-N-terminal kinase prevented suppression of ENaC. Finally, therapeutic inhibition of MEK1/2 restored electrogenic sodium absorption in CD.

CONCLUSIONS

In CD, macroscopically noninflamed colon contributes to diarrhea via impaired ENaC-mediated sodium absorption. Inhibition of extracellular signal-regulated kinase might serve as a potential therapeutic strategy for CD diarrhea.

摘要

背景与目的

克罗恩病(CD)是一种慢性炎症性肠病。在本研究中,我们调查了活动期CD患者宏观上无炎症的结肠中通过上皮钠通道(ENaC)进行的钠吸收情况。

方法

使用来自对照组和仅累及小肠的活动期CD患者的乙状结肠活检标本,在尤斯灌流小室中研究通过ENaC的钠转运。通过实时聚合酶链反应和共聚焦显微镜研究ENaC信使核糖核酸表达及亚细胞定位。在大鼠远端结肠中研究促炎细胞因子对ENaC的影响以及通过丝裂原活化蛋白激酶的信号传导。在CD活检标本中研究对丝裂原活化蛋白激酶的治疗性抑制作用。

结果

由于γ-ENaC转录减少,宏观上无炎症的CD结肠中通过ENaC的电致钠吸收严重受损,而ENaC的亚细胞定位未改变。与上皮钠转运受损相反,无炎症的CD结肠中上皮屏障功能未改变,这表明离子的细胞旁渗漏通量对钠吸收减少没有影响。大鼠远端结肠暴露于肿瘤坏死因子α导致电致钠吸收减少,原因是转录性γ-ENaC诱导受损,这与在CD中发现的变化相似。肿瘤坏死因子α的作用依赖于细胞外信号调节激酶1/2,而不依赖于p38或c-Jun氨基末端激酶,因为抑制丝裂原活化蛋白激酶/细胞外调节激酶(MEK)1/2可防止ENaC受到抑制,而抑制p38或c-Jun氨基末端激酶则不能。最后,对MEK1/2的治疗性抑制恢复了CD中的电致钠吸收。

结论

在CD中,宏观上无炎症的结肠通过受损的ENaC介导的钠吸收导致腹泻。抑制细胞外信号调节激酶可能是治疗CD腹泻的一种潜在策略。

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