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Oxidases and oxygenases in regulation of neutrophil redox pathways in Beh?et’s disease patients

机译:中性粒细胞氧化还原途径调节中的氧化酶和氧气酶?等疾病患者

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This study aimed to determine plasma and neutrophil oxidase activities that may contribute to vascular inflammation in Beh?et’s disease (BD) patients. Cyclooxygenase (COX), NADPH oxidase and myeloperoxidase (MPO) activity was determined in neutrophils isolated from BD patients and healthy controls. Functional assay of NADPH oxidase was significantly increased in BD patients, both at basal conditions and in response to fMLP stimulation. There was a significant increase in plasma MPO activity in the disease group as compared to controls. Total COX activity was significantly increased in BD neutrophils. The increase in total COX activity was accompanied with enhanced activity of COX-2, differentiated by using the COX-1 isoform-specific inhibitor SC-560. Neutrophil nitrate/nitrite levels showed no significant difference in BD; however, plasma nitrate/nitrite contents in BD patients were significantly greater compared to controls. In conclusion, increased plasma MPO, neutrophil NADPH and COX activities may contribute to intravascular inflammation documented in BD patients.
机译:该研究旨在确定可能有助于血管炎症的血浆和中性粒细胞氧化酶活性,其疾病(BD)患者。在从BD患者和健康对照中分离的中性粒细胞中测定环加氧基酶(COX),NADPH氧化酶和髓氧化酶(MPO)活性。在基础条件下,BD患者中NADPH氧化酶的功能测定显着增加,并且响应于FMLP刺激。与对照相比,疾病组中的血浆MPO活性显着增加。 BD中性粒细胞中总COX活性显着增加。总COX活性的增加伴随着COX-2的增强活性,通过使用COX-1种类特异性抑制剂SC-560来分化。中性粒细胞硝酸盐/亚硝酸盐水平显示出BD没有显着差异;然而,与对照相比,BD患者中的血浆硝酸盐/亚硝酸盐含量明显更大。总之,增加血浆MPO,中性粒细胞NADPH和COX活性可能导致BD患者中记载的血管内炎症。

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