Inhibition of human sPLA2 and 5-lipoxygenase activities by two neo-clerodane diterpenoids

被引:21
作者
Benrezzouk, R
Terencio, MC
Ferrándiz, ML
San Feliciano, A
Gordaliza, M
del Corral, JMM
de la Puente, ML
Alcaraz, MJ
机构
[1] Univ Valencia, Dept Pharmacol, Fac Pharm, E-46100 Valencia, Spain
[2] Univ Salamanca, Dept Pharmaceut Chem, E-37008 Salamanca, Spain
关键词
neo-clerodane diterpenoids; phospholipase A(2); 5-lipoxygenase; neutrophil degranulation; elastase; Linaria saxatilis;
D O I
10.1016/S0024-3205(99)00119-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The inhibitory effect of two neo-clerodane diterpenoids, E-isolinaridial (EI) and its methylketone derivative (EIM), isolated from Linaria saxatilis var. glutinosa on PLA(2) and other enzyme activities involved in the inflammatory process was studied. Both compounds inhibited human synovial sPLA(2) in a concentration-dependent manner with IC50 values of 0.20 and 0.49 mu M, respectively, similar to scalaradial. Besides, these compounds decreased the cell-free 5-lipoxygenase activity and A23187-induced neutrophil LTB4 biosynthesis. Another function of human neutrophils, such as receptor-mediated degranulation, was also significantly reduced. In contrast, none of the compounds affected superoxide generation in leukocytes, or cyclooxygenase-l, cyclooxygenase-2 and inducible nitric oxide synthase activities in cell-free assays. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:PL205 / PL211
页数:7
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