University of Mascara, 29000, Mascara, Algeria.
Vet Res Commun. 2012 Mar;36(1):29-33. doi: 10.1007/s11259-011-9507-5. Epub 2011 Oct 21.
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.
本研究旨在探讨一系列经典非甾体抗炎药对马中性粒细胞氧化爆发的潜在调节作用,随后通过发光氨或光红素增强化学发光(CL)技术进行监测。 大多数研究药物对发光氨 CL 有显著的剂量依赖性抑制作用。 这种抑制作用在苯丁唑酮和吲哚美辛中非常显著; 而对于阿司匹林,则需要更高的浓度。 酮洛芬在最初的 5 分钟内作用显著,且仅当浓度高于 1mM 时才如此。 吲哚美辛和乙酰水杨酸的作用导致发光氨 CL 的抑制作用呈剂量依赖性。 另一方面,尽管发光氨稍好一些,但苯丁唑酮在使用发光氨或光红素时均表现出抑制作用。 当考虑酮洛芬时,观察到 luminal CL 的抑制作用,但不如其他研究的 NSAIDs 显著。 氟尼辛葡甲胺强烈增强 CL。