Inhibitory effects of phloroglucinol derivatives from Mallotus japonicus on nitric oxide production by a murine macrophage-like cell line, RAW 264.7, activated by lipopolysaccharide and interferon-γ

被引:24
作者
Ishii, R
Horie, M
Saito, K
Arisawa, M
Kitanaka, S
机构
[1] Nihon Univ, Coll Pharm, Funabashi, Chiba 2748555, Japan
[2] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Lab Herbal Garden, Toyama 9300194, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2001年 / 1568卷 / 01期
关键词
Euphorbiaceae; phloroglucinol derivative; macrophage; nitric oxide; Mallotus japonicus;
D O I
10.1016/S0304-4165(01)00203-3
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 of the pericarps of Mallotus japonicus (MJE) inhibited nitric oxide (NO) production by a murine macrophage-like cell fine, RAW 264.7, which was activated by lipopolysaccharide (LPS) and interferon-gamma (IFN-gamma). Seven phloroglucinol derivatives isolated from MJE exhibited inhibitory activity against NO production. Among these phloroglucinol derivatives, isomallotochromanol exhibited strong inhibitory activity toward NO production, exhibiting an IC50 of 10.7 muM. MJE and the phloroglucinol derivatives significantly reduced both the induction of inducible nitric oxide synthase (iNOS) protein and NOS mRNA expression. NO production by macrophages preactivated with LPS and IFN-gamma for 16 h was also inhibited by MJE and the phloroglucinol derivatives. Furthermore, MJE and the derivatives directly affected the conversion of 1-[C-14]arginine to 1-[C-14]eitrulline by the cell extract. These results suggest that MJE and the phloroglucinol derivatives have the pharmacological ability to suppress NO production by activated macrophages. They inhibited NO production by two mechanisms: reduction of iNOS protein induction and inhibition of enzyme activity. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:74 / 82
页数:9
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