β2-adrenergic receptor stimulation inhibits LPS-induced IL-18 and IL-12 production in monocytes

被引:31
作者
Mizuno, K
Takahashi, HK
Iwagaki, H
Katsuno, G
Kamurul, HASM
Otani, S
Mori, S
Yoshino, T
Nishibori, M
Tanaka, N
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Pharmacol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med & Dent, Dept Surg Gastroenterol, Okayama 7008558, Japan
[3] Okayama Univ, Grad Sch Med & Dent, Dept Pathol, Okayama 7008558, Japan
关键词
adrenergic receptor; IL-18; IL-12;
D O I
10.1016/j.imlet.2005.05.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We examined the effects of beta 2-adrenergic receptor (beta 2-AR) agonists on monocyte-derived cytokines, interleukin (IL)-18 and IL-12 production in lipopolysaccharide, (LPS)-stimulated monocytes derived from human peripheral blood mononuclear cells (PBMCs), as in vitro model of sepsis. The study found that beta 2-AR agonists inhibited IL-18 and IL-12 production in monocytes, and that AR agonist activity was antagonized by the selective beta 2-AR antagonist, butoxamine. The selective beta 2-AR agonists salbutamol and terbutaline induced a similar inhibitory pattern of IL-18 and IL-12 production. IL-12 production induced by LPS was inhibited by anti-IL-18 Ab, but IL-18 production by LPS was not inhibited by anti-IL-12 Ab, showing that LPS induced IL-18 production without IL-12 production. Therefore, the stimulation of beta 2-AR might be beneficial in the treatment of sepsis through inhibiting LPS-elicited IL-18. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:168 / 172
页数:5
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