CATECHOLAMINES INHIBIT LEUKOTRIENE FORMATION AND DECREASE LEUKOTRIENE PROSTAGLANDIN RATIO

被引:20
作者
PARANTAINEN, J
ALANKO, J
MOILANEN, E
METSAKETELA, T
ASMAWI, MZ
VAPAATALO, H
机构
[1] UNIV TAMPERE, DEPT BIOMED SCI, SF-33101 TAMPERE 10, FINLAND
[2] UNIV SAINS MALAYSIA, SCH PHARMACEUT SCI, George Town 11800, MALAYSIA
关键词
D O I
10.1016/0006-2952(90)90480-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Adrenaline, noradrenaline, isoprenaline, and to a lesser extent dopamine inhibit the release of leukotriene (LT) B4 from calcium ionophore-stimulated human polymorphonuclear leukocytes, while the release of prostaglandin (PG) E2 is proportionally elevated. The inactivity of salbutamol, a non-catechol adrenergic β2-receptor agonist, and the inability of propranolol to antagonize the effects of adrenaline, suggest the mediation through β-receptor independent mechanisms. Neither are α-1-receptors involved, as prazosin, a specific antagonist, fails to inhibit the reaction. As the principles for biochemical regulation of LT- and PG-production are met by catecholamines in several tissues, the mechanism is considered to be of general physiological importance. Catecholamines may function as coenzymes/antioxidants which, by altering the redox state of the enzyme iron or heme, decrease the LT/ PG ratio thus protecting the organism against tissue anaphylaxis and other LT-related pathophysiology. © 1990.
引用
收藏
页码:961 / 966
页数:6
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