EICOSANOID PRODUCTION BY RAT CEREBRAL ENDOTHELIAL-CELLS - STIMULATION BY LIPOPOLYSACCHARIDE, INTERLEUKIN-1 AND INTERLEUKIN-6

被引:58
作者
DEVRIES, HE
HOOGENDOORN, KH
VANDIJK, J
ZIJLSTRA, FJ
VANDAM, AM
BREIMER, DD
VANBERKEL, TJC
DEBOER, AG
KUIPER, J
机构
[1] LEIDEN UNIV, SYLVIUS LABS, AMSTERDAM CTR DRUG RES, DIV PHARMACOL, 2300 RA LEIDEN, NETHERLANDS
[2] LEIDEN UNIV, SYLVIUS LABS, AMSTERDAM CTR DRUG RES, DIV BIOPHARMACEUT, 2300 RA LEIDEN, NETHERLANDS
[3] ERASMUS UNIV ROTTERDAM, DEPT PHARMACOL, 3000 DR ROTTERDAM, NETHERLANDS
[4] FREE UNIV AMSTERDAM, FAC MED, DEPT PHARMACOL, 1081 BT AMSTERDAM, NETHERLANDS
关键词
BLOOD-BRAIN BARRIER; INFLAMMATION; CEREBRAL ENDOTHELIAL CELLS; EICOSANOIDS;
D O I
10.1016/0165-5728(95)00009-Q
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The capacity of rat cerebral endothelial cells (RCEC) to form eicosanoids was determined after incubation with C-14-labelled arachidonic acid. Prostaglandin E(2) (PGE(2)) was the main metabolite formed by RCEC and was responsible for 54% of the total amount of eicosanoids produced. In contrast, in primary cultures of rat aorta endothelial cells, 32% of the amount of prostaglandins was 6-keto-PGF(1 alpha). RCEC treated with 50 ng/ml LPS for 24 h responded with an augmented PGE(2) synthesis and 6-keto-PGF(1 alpha) of 3.4-fold and 2.2-fold, respectively. Cultures treated with IL-1 beta (50 ng/ml) for 3 h showed a stimulation of the release of PGE, and 6-keto-PGF(1 alpha) of 2.5- and 4.5-fold, respectively, and 2.0-fold and 2.3-fold, respectively, after IL-6 (50 ng/ml) incubation fdr 3 h. PGE(2) is the main eicosanoid formed by RCEC in response to inflammatory agents, suggesting an important role of the cerebral endothelial cells in the transduction of an inflammatory response in the central nervous system.
引用
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页码:1 / 8
页数:8
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