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[溃疡性结肠炎患者结肠黏膜中核因子-κB的激活及其与细胞因子基因表达的关系]

[Activation of nuclear factor-kappaB and its relationship with cytokine gene expression in colonic mucosa of ulcerative colitis patients].

作者信息

Gan Huatian, Ouyang Qin, Jia Daoquan, Xia Qingjie

机构信息

Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Zhonghua Nei Ke Za Zhi. 2002 Apr;41(4):252-5.

Abstract

OBJECTIVE

To investigate the activation of nuclear factor-kappaB (NF-kappaB) and its relationship with expression of cytokine mRNA in intestinal mucosal biopsy specimens from patients with ulcerative colitis (UC).

METHODS

31 cases with UC were included in the study. 17 cases received sulfasalazine (SASP) or SASP and glucocorticoid treatment. 14 cases did not receive any medication related with UC. Normal mucosa from 11 colon cancer cases served as control. Ten pieces of intestinal mucosal biopsy specimens were obtained from each patient. NF-kappaB DNA binding activity was evaluated with electrophoretic mobility shift assay (EMSA). Expression of cytokine mRNA were studied with reversal tanscription-polymerase chain reaction (RT-PCR).

RESULTS

(1) The expression of IL-1beta mRNA and IL-8 mRNA was increased significantly in patients with UC, as compared with that in the control specimens (P < 0.05) and had a significant positive correlation with NF-kappaB DNA binding activity (r = 0.8363, P < 0.05; r = 0.6024, P < 0.05, respectively). (2) Glucocorticoids and SASP strongly inhibited NF-kappaB activation and signficantly decreased the expression of IL-1beta mRNA and IL-8 mRNA.

CONCLUSIONS

NF-kappaB is a major and essential factor in regulating the expression of cytokine and plays a fundamental role in the pathogenesis of UC. SASP and glucocorticoids decrease cytokine expression via inhibition of NF-kappaB activation.

摘要

目的

研究溃疡性结肠炎(UC)患者肠黏膜活检标本中核因子-κB(NF-κB)的激活情况及其与细胞因子mRNA表达的关系。

方法

本研究纳入31例UC患者。17例接受柳氮磺胺吡啶(SASP)或SASP与糖皮质激素联合治疗。14例未接受任何与UC相关的药物治疗。选取11例结肠癌患者的正常黏膜作为对照。每位患者获取10份肠黏膜活检标本。采用电泳迁移率变动分析(EMSA)评估NF-κB DNA结合活性。运用逆转录-聚合酶链反应(RT-PCR)研究细胞因子mRNA的表达。

结果

(1)与对照标本相比,UC患者IL-1β mRNA和IL-8 mRNA的表达显著增加(P < 0.05),且与NF-κB DNA结合活性呈显著正相关(r分别为0.8363,P < 0.05;r为0.6024,P < 0.05)。(2)糖皮质激素和SASP强烈抑制NF-κB激活,并显著降低IL-1β mRNA和IL-8 mRNA的表达。

结论

NF-κB是调节细胞因子表达的主要且关键因素,在UC发病机制中起重要作用。SASP和糖皮质激素通过抑制NF-κB激活来降低细胞因子表达。

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