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Interactions of sulindac and its metabolites with phospholipid membranes: an explanation for the peroxidation protective effect of the bioactive metabolite.

机译:舒林酸及其代谢产物与磷脂膜的相互作用:生物活性代谢产物过氧化保护作用的解释。

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摘要

Non-steroidal anti-inflammatory drugs (NSAIDs) treat inflammatory processes by inhibition of cycloxygenase (COX). However, their action against lipid peroxidation can be an alternative pathway to COX inhibition. Since inflammation and lipid peroxidation are cell-surface phenomena, the effects of NSAIDs on membrane models were investigated. Peroxidation was induced by peroxyl radical (ROO*) derived from AAPH and assessed in aqueous or lipid media using fluorescence probes with distinct lipophilic properties: fluorescein; HDAF and DPH-PA. The antioxidant effect of Sulindac and its metabolites was tested and related with their membrane interactions. Drug-membrane interactions included the study of: drug location by fluorescence quenching; drug interaction with membrane surface by zeta-potential measurements; and membrane fluidity changes by steady-state anisotropy. Results revealed that the active NSAID (sulindac sulphide) penetrates into the lipid bilayer and protects the membrane against oxy-radicals. The inactive forms (sulindac and sulindac sulphone) present weaker interactions with the membrane and are better radical scavengers in aqueous media.
机译:非甾体类抗炎药(NSAIDs)通过抑制环氧合酶(COX)来治疗炎症过程。但是,它们对脂质过氧化的作用可能是抑制COX的另一种途径。由于炎症和脂质过氧化是细胞表面现象,因此研究了NSAIDs对膜模型的影响。过氧化是由源自AAPH的过氧自由基(ROO *)诱导的,并使用具有独特亲脂特性的荧光探针在水性或脂质介质中进行评估: HDAF和DPH-PA。测试了舒林酸及其代谢产物的抗氧化作用,并与其膜相互作用有关。药物-膜相互作用包括以下方面的研究:通过荧光猝灭进行药物定位;通过ζ电势测量药物与膜表面的相互作用;膜的流动性因稳态各向异性而改变。结果表明,活性NSAID(舒林酸硫化物)渗透到脂质双层中,并保护膜免受氧自由基的侵害。非活性形式(舒林酸和舒林酸砜)与膜的相互作用较弱,在水性介质中是较好的自由基清除剂。

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