Hashizume H, Tokura Y, Oku T, Iwamoto Y, Takigawa M
Division of Dermatology, National Tousei Hospital, Shizuoka, Japan.
Arch Dermatol Res. 1995;287(6):586-90. doi: 10.1007/BF00374081.
Various drugs and chemicals break the DNA strand under ultraviolet irradiation. This study aimed to clarify the DNA-breaking activity (DBA) of serum from 39 patients with various photosensitivity disorders and that from eight normal subjects. A mixture of serum and circular plasmid DNA was exposed to longwave ultraviolet radiation, and the photoinduced cleavage of plasmid DNA was examined by electrophoretic analysis. DBA was found in serum from patients with erythropoietic protoporphyria (2 of 2), drug-induced photosensitivity (3 of 5), chronic actinic dermatitis (1 of 12) and hydroa vacciniforme (1 of 1). DBA was not found in serum from patients with porphyria cutanea tarda, collagen diseases with photosensitivity, papulovesicular light eruption or pellagra. The inhibition profile of DBA by active oxygen scavengers was different between afloqualone- and tetracycline-induced photosensitivity and chronic actinic dermatitis. The present method was useful for the detection of serum phototoxicity and the investigation of the pathomechanisms of photosensitivity.
多种药物和化学物质在紫外线照射下会使DNA链断裂。本研究旨在阐明39例各种光敏性疾病患者及8名正常受试者血清的DNA断裂活性(DBA)。将血清与环状质粒DNA的混合物暴露于长波紫外线辐射下,通过电泳分析检测质粒DNA的光诱导切割。在红细胞生成性原卟啉病患者(2例中的2例)、药物性光敏反应(5例中的3例)、慢性光化性皮炎(12例中的1例)和种痘样水疱病(1例中的1例)患者的血清中发现了DBA。在迟发性皮肤卟啉病、光敏性胶原病、丘疹水疱性光疹或糙皮病患者的血清中未发现DBA。活性氧清除剂对afloqualone和四环素诱导的光敏反应以及慢性光化性皮炎的DBA抑制谱不同。本方法可用于检测血清光毒性及研究光敏性的发病机制。