Morison W L, Paul B S, Parrish J A
J Invest Dermatol. 1977 Mar;68(3):130-3. doi: 10.1111/1523-1747.ep12492445.
Indomethacin, a known inhibitor of prostaglandin synthesis, administered topically as a 2.5% solution, intradermally in 10 mug doses, and orally in a dose of 150 mg/day for 2 days did not diminish the delayed erythema produced a long-wave ultraviolet light (320-400 nm). The delayed phototoxic erythema produced by 8-methoxypsoralen and subsequent exposure the long-wave ultraviolet light was similarly unaffected. By comparison, topical and intradermal indomethacin treatment produced sustained decrease in the erythemal response to ultraviolet radiation in the UVB ranges (290-320 nm).
吲哚美辛是一种已知的前列腺素合成抑制剂,以2.5%的溶液局部给药,皮内注射剂量为10微克,口服剂量为150毫克/天,持续2天,并未减轻长波紫外线(320 - 400纳米)产生的延迟性红斑。8-甲氧基补骨脂素产生的延迟性光毒性红斑以及随后暴露于长波紫外线的情况同样未受影响。相比之下,局部和皮内吲哚美辛治疗使对UVB范围(290 - 320纳米)紫外线辐射的红斑反应持续降低。