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Ursodeoxycholate inhibits induction of NOS in human intestinal epithelial cells and in vivo.

作者信息

Invernizzi P, Salzman A L, Szabó C, Ueta I, O'Connor M, Setchell K D

机构信息

Clinical Mass Spectrometry Center, Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

出版信息

Am J Physiol. 1997 Jul;273(1 Pt 1):G131-8. doi: 10.1152/ajpgi.1997.273.1.G131.

DOI:10.1152/ajpgi.1997.273.1.G131
PMID:9252519
Abstract

Ursodeoxycholate (UDCA) has anti-inflammatory and chemoprotective effects in animal models of inflammatory bowel disease and colon cancer. Because overproduction of nitric oxide (NO) by the inducible isoform of NO synthase (iNOS) is implicated in the pathogenesis of these conditions, we investigated the ability of UDCA to inhibit NO production in transformed human intestinal epithelial (DLD-1) cells. Nitrite/nitrate production was measured by the Griess reaction, enzymatic activity of iNOS was assessed by conversion of L-arginine to L-citrulline, and protein and mRNA were measured by Western and Northern blotting. Dose-dependent inhibition of interleukin-1 beta- and interferon-gamma-stimulated nitrite/nitrate production was observed when cells were preincubated for 6 h with UDCA (0-800 microM), and a substantial inhibition (81 +/- 3.2%) was seen at 500 microM. In cytokine-stimulated cells, UDCA reduced iNOS mRNA, protein, and enzyme activity without exerting cytotoxicity. UDCA had a minimal direct inhibitory effect on iNOS enzyme activity. UDCA pretreatment also reduced the expression of iNOS in the colonic epithelium of rats treated with bacterial lipopolysaccharide. Thus UDCA inhibits the induction of epithelial iNOS in vitro and in vivo, and this effect may contribute to the anti-inflammatory and chemoprotective actions of UDCA.

摘要

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Nitric oxide-mediated intestinal injury is required for alcohol-induced gut leakiness and liver damage.
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Dig Dis Sci. 2008 Jun;53(6):1437-42. doi: 10.1007/s10620-007-0061-5.
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Ursodeoxycholic acid suppresses extent of lipid peroxidation in diseased liver in experimental cholestatic liver disease.熊去氧胆酸可抑制实验性胆汁淤积性肝病中病肝的脂质过氧化程度。
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