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首页> 外文期刊>Veterinary Research Communications >Modulatory effects of non-steroidal anti-inflammatory drugs on the luminol and lucigenin amplified chemiluminescence of equine neutrophils
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Modulatory effects of non-steroidal anti-inflammatory drugs on the luminol and lucigenin amplified chemiluminescence of equine neutrophils

机译:非甾体抗炎药对鲁米酚和鳞蜥的调节作用扩增大二嗜中性粒细胞的化学发光

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摘要

The purpose of this study was to explore the potential modulation of equine neutrophil oxidative burst by a series of classical NSAIDs which was subsequently monitored by the luminol or lucigenin-enhanced chemiluminescence (CL) technique. A significant dose-dependent inhibition of the luminol CL was observed with the majority of investigated drugs. This inhibition was very significant for phenylbutazone and Indomethacin; while for aspirin, a higher concentration is required. The action of Ketoprofen was significant during the first 5 min and only when the concentration was above 1 mM. Indomethacin and acetylsalicylic acid result in an inhibition dose-dependent of luminol CL. On the other hand, the phenylbutazone showed an inhibiting effect when used either luminol or lucigenin though luminol is slightly better. When the ketoprofen is considered, an inhibiting effect of luminal CL was observed but less significant than the other NSAIDs investigated. The flunixin meglumine enhances strongly the CL.
机译:本研究的目的是探讨马中性粒细胞氧化爆发的一系列经典NSAID的潜在调节,该型古典NSAID被鲁米酚或肠素增强的化学发光(CL)技术监测。用大多数研究药物观察到鲁米诺克隆的显着剂量依赖性抑制。这种抑制对于苯二丁酮和吲哚美辛非常显着;虽然对于阿司匹林,但需要更高的浓度。酮洛芬的作用在前5分钟内显着,并且仅当浓度高于1mm时。吲哚美辛和乙酰胱氨酸酸导致抑制剂量依赖于Luminol Cl。另一方面,当荧光醇略好时,苯基丁嗪在使用鲁米酚或尿苷时显示出抑制作用。考虑酮洛芬时,观察到腔C1的抑制作用,但比所研究的其他NSAID较小。弗卢其汀菌丝强烈增强了CL。

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