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吲哚美辛对人抗IgE晚期反应的抑制作用。

Inhibition of the late phase response to anti-IgE in humans by indomethacin.

作者信息

Grönneberg R, Zetterström O

出版信息

Allergy. 1985 Jan;40(1):36-41. doi: 10.1111/j.1398-9995.1985.tb04152.x.

Abstract

The hypothesis of cyclooxygenase derivates of arachidonic acid as putative mediators of late phase skin reactions (LPR) was evaluated by studying the effect of indomethacin and naproxen on anti-IgE elicited skin reactions in healthy volunteers. Indomethacin 50 mg t.i.d., 48 h prior to and up to 24 h following challenge with anti-IgE 1/3300 (v/v), produced a slight attenuation of the flare response and a 35% inhibition of the LPR (P less than 0.05) at 1-24 h as compared with placebo (n = 11). Naproxen, 250 mg, b.i.d. showed analogous anti-LPR effect (n = 4, P less than 0.05). Intradermally (i.d.) injected indomethacin, 75 micrograms (7 X 10(-3) mol/l), attenuated the flare and LPR to anti-IgE 1/330 at 1-6 h (n = 12, P less than 0.01). Indomethacin, oral and i.d., enhanced the LPR to various dilutions of anti-IgE in 30% of the individuals. The results suggest that prostaglandins and thromboxanes participate in the development of an LPR in human skin.

摘要

通过研究吲哚美辛和萘普生对健康志愿者抗IgE引发的皮肤反应的影响,评估了花生四烯酸的环氧化酶衍生物作为迟发性皮肤反应(LPR)假定介质的假说。在使用1/3300(v/v)抗IgE激发前48小时至激发后24小时,口服吲哚美辛50mg,每日3次,与安慰剂相比(n = 11),在1 - 24小时时,红斑反应略有减弱,LPR受到35%的抑制(P < 0.05)。萘普生250mg,每日2次,显示出类似的抗LPR作用(n = 4,P < 0.05)。皮内注射75μg(7×10⁻³mol/L)吲哚美辛,在1 - 6小时时减弱了对1/330抗IgE的红斑和LPR反应(n = 12,P < 0.01)。口服和皮内注射吲哚美辛,在30%的个体中增强了对不同稀释度抗IgE的LPR反应。结果表明,前列腺素和血栓烷参与了人类皮肤LPR的发生发展。

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