...
首页> 外文期刊>European journal of gastroenterology and hepatology >Gluten-induced nitric oxide and pro-inflammatory cytokine release by cultured coeliac small intestinal biopsies.
【24h】

Gluten-induced nitric oxide and pro-inflammatory cytokine release by cultured coeliac small intestinal biopsies.

机译:麸质诱导的一氧化氮和促炎性细胞因子的释放通过培养的腹腔小肠活检组织。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

OBJECTIVES: To determine whether there was increased nitric oxide (NO) production from coeliac small intestinal biopsies cultured in vitro with gluten and whether the inhibition of NO production could prevent gluten-induced enterotoxicity. The relationship between NO production with the pro-inflammatory cytokines interferon-gamma (IFN-gamma), tumour necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) was evaluated. DESIGN: Small intestinal biopsies from ten patients with treated coeliac disease and six controls were studied. METHODS: Small intestinal biopsies were taken from each patient and set up in culture with Frazer's fraction III (FFIII), a peptic/tryptic digest of gluten, FFIII plus L-NMMA and L-NMMA alone, culture medium alone and ovalbumin which served as a control protein. The biopsies were cultured for 20 h at 37 degrees C. The supernatants were then collected and analysed for nitrite using the Greiss reaction; cytokine levels were determined using ELISA kits. Enterocyte height was determined by microscopy using a calibrated eyepiece graticule and cryostat sections of the cultured biopsies. RESULTS: Coeliac biopsies cultured with FFIII produced significantly greater nitrite compared to culture medium alone (P< 0.05) and this could be blocked with L-NMMA (P< 0.01). A reduction in enterocyte height was seen in coeliac biopsies cultured with FFIII compared to culture medium alone (P < 0.01) and this was ameliorated but not completely blocked when FFIII was cultured with L-NMMA. These changes were not seen in the controls. There was a significant reduction in IL-1beta levels in the supernatant of coeliac biopsies cultured with FFIII compared to culture medium alone (P< 0.05), but when cultured with FFIII and L-NMMA there was a significant increase in IL-1beta levels (P< 0.05). An increase in IFN-gamma levels was also seen when coeliac biopsies were cultured with FFIII and L-NMMA (P< 0.05). This pattern was not seen with TNF-alpha. CONCLUSIONS: Increased levels of NO can be found when coeliac biopsies are cultured with gluten in an in vitro small intestinal culture system, and NO may play a role in the observed enterotoxicity as the inhibition of NO production ameliorates the enterocyte damage. The results suggest that NO is involved in the regulation of pro-inflammatory cytokines, particularly IL-1beta. This is likely to be one of many pathways leading to the observed mucosal pathology in coeliac disease and demonstrates the close interactions between them.
机译:目的:确定体外用麸质培养的腹腔小肠活检组织中一氧化氮(NO)的产生是否增加,以及是否抑制NO的产生是否可以防止麸质引起的肠毒性。评估NO产生与促炎细胞因子干扰素-γ(IFN-γ),肿瘤坏死因子-α(TNF-α)和白介素-1β(IL-1β)之间的关系。设计:研究了来自十名患有乳糜泻的患者和六个对照组的小肠活检。方法:从每位患者中取出小肠活检组织,并与弗雷泽氏级分(FFIII),面筋的消化/胰消化液,FFIII加L-NMMA和L-NMMA单独,单独的培养基和卵清蛋白一起培养。对照蛋白。在37℃下将活组织检查样品培养20小时。然后收集上清液,并使用Greiss反应分析亚硝酸盐。用ELISA试剂盒测定细胞因子水平。肠上皮细胞的高度通过显微镜检查,使用经校准的目镜刻度和培养的活检切片的低温恒温器切片确定。结果:与单独的培养基相比,用FFIII培养的腹腔活检组织产生的亚硝酸盐明显更多(P <0.05),并且可以被L-NMMA阻断(P <0.01)。与单独的培养基相比,在用FFIII培养的腹腔穿刺活检中发现肠细胞高度降低(P <0.01),当用L-NMMA培养FFIII时,这种情况得到了改善,但并未完全被阻止。这些更改未在控件中看到。与单独的培养基相比,用FFIII培养的腹腔穿刺活检上清液中IL-1beta水平显着降低(P <0.05),但是当用FFIII和L-NMMA培养时,IL-1beta水平显着增加( P <0.05)。当腹腔穿刺活检与FFIII和L-NMMA培养时,IFN-γ水平也增加(P <0.05)。 TNF-α未见此模式。结论:在体外小肠培养系统中,将麸质活检与麸质一起培养时,可以发现NO含量升高,并且NO可能在观察到的肠毒性中发挥作用,因为抑制NO的产生可以减轻肠细胞的损害。结果表明NO参与促炎细胞因子,特别是IL-1beta的调节。这很可能是导致腹腔疾病粘膜病理的许多途径之一,并证明了它们之间的密切相互作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号