Prostaglandin E2 production and induction of prostaglandin endoperoxide synthase-2 is inhibited in a murine macrophage-like cell line, RAW 264.7, by Mallotus japonicus phloroglucinol derivatives

被引:20
|
作者
Ishii, R
Horie, M
Saito, K
Arisawa, M
Kitanaka, S
机构
[1] Nihon Univ, Coll Pharm, Funabashi, Chiba 2748555, Japan
[2] Saitama Inst Publ Hlth, Urawa, Saitama 3380824, Japan
[3] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Lab Herbal Garden, Toyama 9300194, Japan
来源
关键词
Mallotus japonicus; Euphorbiaceae; phloroglucinol derivative; macrophage; prostaglandin E-2; prostaglandin endoperoxide synthase;
D O I
10.1016/S0304-4165(02)00200-3
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
An aqueous acetone extract obtained from the pericarps of Mallotus japonicus (MJE) was observed to inhibit prostaglandin (PG) E, production in a lipopolysaccharide (LPS)-activated murine macrophage-like cell line, RAW 264.7. Six phloroglucinol derivatives isolated from MJE exhibited inhibitory activity against PGE(2) production. Among these phloroglucinol derivatives, isomallotochromanol showed the strongest inhibitory activity, with an IC50 of 1.0 muM. MJE and its phloroglucinol derivatives did not effect the enzyme activity of either prostaglandin endoperoxide synthase (PGHS)-1 or PGHS-2. However, induction of PGHS-2 in LPS-activated macrophages was inhibited by MJE and its phloroglucinol derivatives, whereas the level of PGHS-1 protein was not affected. Moreover, RT-PCR analysis showed that WE and its phloroglucinol derivatives significantly suppressed PGHS-2 mRNA expression, Therefore, the observed inhibition of PGHS-2 induction by WE and its phloroglucinol derivatives was likely due to a suppression of PGHS-2 mRNA expression. These results suggest that MJE and its phloroglucinol derivatives have the pharmacological ability to suppress PGE(2) production by activated macrophages. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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