BETA-ADRENERGIC RECEPTORS MEDIATE IN-VIVO THE ADRENALINE INHIBITION OF LIPOPOLYSACCHARIDE-INDUCED TUMOR-NECROSIS-FACTOR RELEASE

Citation
G. Monastra et Ef. Secchi, BETA-ADRENERGIC RECEPTORS MEDIATE IN-VIVO THE ADRENALINE INHIBITION OF LIPOPOLYSACCHARIDE-INDUCED TUMOR-NECROSIS-FACTOR RELEASE, Immunology letters, 38(2), 1993, pp. 127-130
Citations number
26
Categorie Soggetti
Immunology
Journal title
ISSN journal
01652478
Volume
38
Issue
2
Year of publication
1993
Pages
127 - 130
Database
ISI
SICI code
0165-2478(1993)38:2<127:BRMITA>2.0.ZU;2-T
Abstract
Adrenaline has been shown to inhibit the release of tumor necrosis fac tor (TNF) elicited by lipopolysaccharide (LPS) when tested in vitro on cultured human blood cells and rat macrophages. In this report we hav e examined the effect of the in vivo administration of adrenaline on T NF serum levels induced by LPS. In agreement with in vitro data, adren aline (0.1 mg/kg, s.c.) was found to inhibit in the mouse the LPS-indu ced TNF release. The beta-adrenergic antagonist propranolol administer ed 1 h before adrenaline completely blocked the adrenaline activity, w hereas the alpha-adrenergic antagonist phentolamine was ineffective. T hese data demonstrate that: (i) adrenaline is an effective antagonist of LPS-induced TNF release in vivo, and (ii) its effect is mediated by adrenergic receptors.