TOPICAL GLUCOCORTICOIDS INHIBIT NEUROGENIC INFLAMMATION - INVOLVEMENT OF LIPOCORTIN-1

被引:19
作者
AHLUWALIA, A [1 ]
NEWBOLD, P [1 ]
BRAIN, SD [1 ]
FLOWER, RJ [1 ]
机构
[1] UNIV LONDON KINGS COLL,DIV BIOMED SCI,PHARMACOL & VASC BIOL RES CTR,LONDON SW3 6LX,ENGLAND
基金
英国惠康基金;
关键词
LIPOCORTIN; 1; NEUROGENIC INFLAMMATION; EDEMA; TOPICAL GLUCOCORTICOID;
D O I
10.1016/0014-2999(95)00350-T
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Topical glucocorticoid treatment (betamethasone-17-valerate (0.018 mg/cm(2), 3 h pretreatment) significantly inhibited neurogenic oedema formation induced by electrical antidromic stimulation (2 Hz, 15 V, 0.1 ms for 5 min) of the rat saphenous nerve; a response mediated by neuropeptides released from activated capsaicin-sensitive sensory C-fibres. Oedema formation was estimated by measurement of extravasation of i.v. injected I-125-albumin into skin. The inhibitory effect of the topical glucocorticoid was reversed by passive immunisation of rats with polyclonal antibody to the glucocorticoid-inducible anti-inflammmatory protein lipocortin 1 (1 ml/kg, s.c., 24 h pretreatment) whilst a non-immune serum was without effect. Similarly the glucocorticoid receptor antagonist RU38486 (20 mg/kg, 2 and 20 h pretreatment) abrogated the response indicating specific binding to glucocorticoid receptors. Topical glucocorticoid treatment also inhibited the oedema produced by intradermal substance P (0.1 nmol) in the dorsal skin of rats. Topical glucocorticoid inhibited neurogenic oedema formation partly through a mechanism dependent upon lipocortin 1. This inhibition may be partly due to a post-junctional effect upon substance P activity/binding however a pre-junctional component cannot be excluded.
引用
收藏
页码:193 / 198
页数:6
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