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司帕沙星的光毒性:紫外线A和B光源潜在的光增强作用

Sparfloxacin phototoxicity: potential photoaugmentation by ultraviolet A and B sources.

作者信息

Tokura Y, Iwamoto Y, Mizutani K, Takigawa M

机构信息

Department of Dermatology, Hamamatsu University School of Medicine, Japan.

出版信息

Arch Dermatol Res. 1996;288(1):45-50. doi: 10.1007/BF02505042.

Abstract

Sparfloxacin, a quinolone antibacterial agent, frequently elicits photosensitive skin reactions. Our clinical studies of patients treated with sparfloxacin have demonstrated that this photosensitivity is primarily phototoxic and that a marked erythematous response is induced by sequential irradiation with ultraviolet A (UVA) and B (UVB) but not UVA or UVB alone, suggesting potential synergism between UVA and UVB. We evaluated the phototoxicity of this agent using in vitro DNA breaking activity and in vivo murine cutaneous responses. Sparfloxacin induced DNA strand breaks in vitro and converted the supercoiled closed circular form of plasmid DNA to the open circular form by its photodynamic action. In mice, the topical application of sparfloxacin and subsequent irradiation with UVB, but not UVA, induced ear swelling responses. However, the UVB-induced ear swelling response was augmented by irradiation with UVA before or after UVB exposure. Such interaction between UVA and UVB in the production of ear swelling was further confirmed by systemic administration of sparfloxacin. Our study suggests that sparfloxacin is a unique phototoxic agent in that photosensitivity dermatitis is evoked by photoaugmentation between UVA and UVB.

摘要

司帕沙星是一种喹诺酮类抗菌剂,常引起光敏性皮肤反应。我们对接受司帕沙星治疗的患者进行的临床研究表明,这种光敏性主要是光毒性的,并且紫外线A(UVA)和紫外线B(UVB)顺序照射可诱导明显的红斑反应,而单独的UVA或UVB照射则不会,这表明UVA和UVB之间存在潜在的协同作用。我们使用体外DNA断裂活性和体内小鼠皮肤反应来评估该药物的光毒性。司帕沙星在体外诱导DNA链断裂,并通过其光动力作用将质粒DNA的超螺旋闭环形式转化为开环形式。在小鼠中,局部应用司帕沙星并随后用UVB照射,而不是UVA照射,可诱导耳部肿胀反应。然而,在UVB暴露之前或之后用UVA照射可增强UVB诱导的耳部肿胀反应。司帕沙星全身给药进一步证实了UVA和UVB在耳部肿胀产生中的这种相互作用。我们的研究表明,司帕沙星是一种独特的光毒性药物,因为UVA和UVB之间的光增强作用会引发光敏性皮炎。

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