Subacute treatment of rats with dexamethasone reduces ICAM-1 levels on circulating monocytes

被引:27
作者
Tailor, A [1 ]
Das, AM [1 ]
Getting, SJ [1 ]
Flower, RJ [1 ]
Perretti, M [1 ]
机构
[1] WILLIAM HARVEY RES INST,DEPT BIOCHEM PHARMACOL,LONDON EC1M 6BQ,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1006/bbrc.1997.6168
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report for the first time that in vivo treatment with dexamethasone (DEX) reduces levels of intercellular adhesion molecule-1 (ICAM-1) expression on rat circulating unstimulated monocytes (-55%) and peritoneal macrophages (-26%), This effect was present following sub-acute (5 days) treatment with a low dose (0.1 mg/kg per day), but not after single administration of a high dose (1 mg/kg, -2 h), of the steroid. Both acute and sub-acute treatment with DEX failed 60 modify either basal or up-regulated CD11b expression on peripheral blood monocytes and neutrophils, elastase release from neutrophils, and beta-glucuronidase release from cultured macrophages. The lack of alteration of CD11b expression on circulating leukocytes suggests that the effect of DEX on ICAM-1 expression is secondary to gene repression rather than a non-specific blockade of cell differentiation. These data promote the concept that different dose-regimens with glucocorticoids affect distinct molecular targets and indicate that clinically-related protocols of DEX may reveal new mechanism(s) of action. (C) 1997 Academic press.
引用
收藏
页码:675 / 678
页数:4
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