The effects of noradrenaline and alpha-2 adrenoceptor agents on the production of monocytic products

被引:79
作者
Maes, M
Lin, AH
Kenis, G
Egyed, B
Bosmans, E
机构
[1] Univ Hosp, Dept Psychiat & Neuropsychol, NL-6202 AZ Maastricht, Netherlands
[2] Clin Res Ctr Mental Hlth, Antwerp, Belgium
[3] Vanderbilt Univ, Dept Psychiat, Nashville, TN USA
[4] Eurogenet, Tessenderlo, Belgium
关键词
cytokines; interleukin-6; interleukin-1 receptor antagonist; tumor necrosis factor; catecholamines; noradrenaline; clonidine; alpha-adrenergic receptors;
D O I
10.1016/S0165-1781(00)00216-X
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
There are some reports that catecholamines may modulate the production of monocytic cytokines such as interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF alpha). The present study was carried out in order to examine the effects of noradrenaline (10(-5), 10(-6) and 10(-7) M), clonidine (10(-5), 10(-6) and 10(-7) M), an alpha2-adrenoceptor agonist, and yohimbine (10(-5), 10(-6) and 10(-7) M), an alpha2-adrenoceptor antagonist, on the production of IL-6, the IL-1 receptor antagonist (IL-1RA) and TNF alpha by stimulated whole blood of normal humans. We measured the in vitro production of IL-b, TNF alpha and IL-1RA by stimulated (phytohemagglutinin + lipopolysaccharide), diluted whole blood of 16 normal volunteers, The results show that noradrenaline, 10-5 M, significantly suppressed the production of IL-6; noradrenaline, 10(-5) and 10(-6) M, significantly suppressed the production of IL-1RA and TNF alpha; clonidine, 10(-5) M, significantly suppressed the production of TNF alpha; and yohimbine, 10(-5) and 10(-6) M, significantly suppressed the production of IL-1RA. It is concluded that (1) noradrenaline has significant negative immunoregulatory effects in humans through suppression of the production of (monocytic) proinflammatory cytokines, e.g. IL-6 and TNF alpha, and (2) the suppression of the production of TNF alpha may be related to alpha (2)-adrenoceptor-related mechanisms. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:245 / 253
页数:9
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