Ternowitz T, Fogh K, Kragballe K
Department of Dermatology, Marselisborg Hospital, University of Aarhus, Denmark.
Skin Pharmacol. 1988;1(2):93-9. doi: 10.1159/000210754.
15-Hydroxyeicosatetraenoic acid (15-HETE), a 15-lipoxygenase (15-LO) product of arachidonic acid has the potential to inhibit leukotriene formation. In the present study the effect of 15-HETE on leukotriene B4 (LTB4)-induced polymorphonuclear leukocytes (PMN) and monocyte chemotaxis was investigated. LTB4-induced chemotaxis of PMNs was inhibited in a dose-dependent manner by 15-HETE. Maximum inhibition (68%) occurred at a 15-HETE concentration of 10(-4) M. The 15-LO product of eicosapentaenoic acid (15-HEPE) was approximately 10 times less potent in inhibiting LTB4-induced PMN chemotaxis. LTB4-induced chemotaxis of monocytes was unaffected by both 15-HETE and 15-HEPE. Using N-formyl-methionyl-leucyl-phenylalanine (FMLP) and complement split product C5a as chemoattractants, 15-HETE did not decrease PMN chemotaxis. Furthermore, 15-HETE itself did not affect random migration of leukocytes. The present results demonstrate that 15-HETE inhibits LTB4-induced chemotaxis of PMNs in vitro in a specific and selective way. Because 15-HETE not only inhibits formation, but also the effect of LTB4, it may be important in regulating LTB4-induced inflammation.
15-羟基二十碳四烯酸(15-HETE)是花生四烯酸的15-脂氧合酶(15-LO)产物,具有抑制白三烯形成的潜力。在本研究中,研究了15-HETE对白三烯B4(LTB4)诱导的多形核白细胞(PMN)和单核细胞趋化性的影响。15-HETE以剂量依赖性方式抑制LTB4诱导的PMN趋化性。在15-HETE浓度为10^(-4) M时出现最大抑制(68%)。二十碳五烯酸的15-LO产物(15-HEPE)在抑制LTB4诱导的PMN趋化性方面的效力约低10倍。LTB4诱导的单核细胞趋化性不受15-HETE和15-HEPE的影响。使用N-甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)和补体裂解产物C5a作为趋化剂,15-HETE不会降低PMN趋化性。此外,15-HETE本身不影响白细胞的随机迁移。目前的结果表明,15-HETE在体外以特异性和选择性方式抑制LTB4诱导的PMN趋化性。由于15-HETE不仅抑制LTB4的形成,还抑制其作用,它可能在调节LTB4诱导的炎症中起重要作用。