Effect of vitamin E on expression of cyclooxygenase-2 in lipopolysaccharide-stimulated rat macrophages

被引:18
作者
Sakamoto, W
Fujie, K
Nishihira, J
Handa, H
Ueda, N
Yamamoto, S
机构
[1] HOKKAIDO UNIV,SCH MED,CENT RES INST,SAPPORO,HOKKAIDO 060,JAPAN
[2] TONAN HOSP,SAPPORO,HOKKAIDO 060,JAPAN
[3] UNIV TOKUSHIMA,SCH MED,DEPT BIOCHEM,TOKUSHIMA 770,JAPAN
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1996年 / 1304卷 / 02期
关键词
alpha-tocopherol; macrophage; prostaglandin E(2); cyclooxygenase-2; lipopolysaccharide; vitamin E; (rat peritoneal macrophage);
D O I
10.1016/S0005-2760(96)00114-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To clarify the role of vitamin E (alpha-tocopherol) for the induction of cyclooxygenase-2 (COX-2) in rat macrophages stimulated by lipopolysaccharide (LPS), vitamin E-enriched macrophages were prepared by intraperitoneal injection of vitamin E for 6 days at a rate of 5 mg per day. The production of PGE(2) was increased in dose- and time-dependent manners by addition of LPS in both control and vitamin E-enriched peritoneal macrophages. The maximum effect of LPS was observed in 12 h at concentration of 5 mu g/ml. By analyzing COX-2 mRNA level by Northern blot and COX-2 enzyme mass and phosphotyrosine by Western blot, it was revealed that the increase of PGE(2) production reflected the induction of COX-2 expression through activation of tyrosine kinase. Vitamin E failed to inhibit PGE(2) production in LPS-stimulated macrophages; however, genistein, a tyrosine kinase inhibitor, completely inhibited the production at 100 mu M. These results suggest that vitamin E does not inhibit COX-2 expression via LPS-mediated tyrosine kinase signal transduction pathway.
引用
收藏
页码:139 / 144
页数:6
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