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首页> 外文期刊>Scandinavian journal of gastroenterology. >Expression of inducible nitric oxide synthase and effects of L-arginine on colonic nitric oxide production and fluid transport in patients with minimal colitis
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Expression of inducible nitric oxide synthase and effects of L-arginine on colonic nitric oxide production and fluid transport in patients with minimal colitis

机译:轻度结肠炎患者诱导型一氧化氮合酶的表达及L-精氨酸对结肠一氧化氮产生和输液的影响

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Objective. Some patients with idiopathic, chronic diarrhoea have minimal, non-specific colonic inflammation. As nitric oxide (NO) acts as a secretagogue in the colon, we studied the expression of inducible NO synthase (iNOS) in mucosal biopsies and the effects of NOS stimulation on colonic transfer of fluid and output of NO in patients with "minimal colitis".Material and methods. Twelve patients with idiopathic, chronic diarrhoea and "minimal colitis" and 6 healthy volunteers were included in the study. Expression of iNOS in colonic mucosal biopsies was quantified by Western blot analysis and localized by immunohistochemistry. The effects of topical L-arginine or placebo on colonic net fluid transfer and nitriteitrate (NO(x)) output were assessed during "steady state" perfusion of the whole colon. Concentrations of NO(x) were measured by Griess' assay.Results. The expression of iNOS was increased 10-fold (p<0.01) in patients with "minimal colitis" compared with that in healthy volunteers and localized to the colonic epithelium. Colonic absorption of fluid was impaired (mean (SEM) 1.5 (0.2) versus 3.0 (0.2) ml/min, p<0.001) and the output of NO(x) was increased (47 (4) nmol/min versus <37 nmol/min, p<0.05) in patients with "minimal colitis" compared with that in healthy volunteers. Luminal L-arginine (20 mM) reduced colonic absorption of fluid in both groups (95% confidence intervals (CIs) 21-50% in patients with "minimal colitis" versus 4-18% in healthy volunteers), but an increase in NO(x) output was detectable only in the group of patients (8-106%). In time control experiments, colonic net transfer rates of fluid and outputs of NO(x) were unaffected by placebo.Conclusions. In patients with idiopathic, chronic diarrhoea and histopathological evidence of minimal colitis epithelial expression of iNOS and mucosal production of NO is enhanced. It could be speculated that NO in excess contributes to the diarrhoea observed in "minimal colitis".
机译:目的。一些患有特发性慢性腹泻的患者仅有很少的非特异性结肠炎。由于一氧化氮(NO)充当结肠的促分泌素,我们研究了“最小结肠炎”患者黏膜活检组织中诱导型NO合酶(iNOS)的表达以及NOS刺激对结肠液转移和NO输出的影响。 。材料与方法。这项研究包括了十二位特发性,慢性腹泻和“最小结肠炎”患者和六名健康志愿者。通过蛋白质印迹分析定量iNOS在结肠粘膜活检组织中的表达,并通过免疫组织化学定位。在整个结肠的“稳态”灌注过程中,评估了局部L-精氨酸或安慰剂对结肠净液转移和亚硝酸盐/硝酸盐(NO(x))输出的影响。通过Griess法测定NO(x)的浓度。结果。与健康志愿者相比,“最小结肠炎”患者中iNOS的表达增加了10倍(p <0.01),并位于结肠上皮细胞中。结肠的液体吸收受到损害(平均值(SEM)1.5(0.2)对3.0(0.2)ml / min,p <0.001),NO(x)的输出增加(47(4)nmol / min对<37 nmol /min,p<0.05)与健康志愿者的“最小结肠炎”患者相比。发光的L-精氨酸(20 mM)降低了两组的结肠液吸收(“最小结肠炎”患者的95%置信区间(CIs)为21-50%,而健康志愿者为4-18%),但NO升高(x)仅在患者组(8-106%)中可检测到输出。在时间控制实验中,结肠液的净净传输速率和NO(x)的输出不受安慰剂的影响。在患有特发性,慢性腹泻的患者中,iNOS的结肠炎上皮最小表达和粘膜NO生成的组织病理学证据得到增强。可以推测,过量的NO导致“最小结肠炎”中的腹泻。

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