The methanol extract of Spiraea prunifolia var, simpliciflora root inhibits the generation of nitric oxide and superoxide in RAW 264.7 cells

被引:20
作者
So, HS
Park, R
Oh, HM
Pae, HO
Lee, JH
Chai, KY
Chung, SY
Chung, HT [1 ]
机构
[1] Wonkwang Univ, Sch Med, Dept Microbiol, Iksan 570749, Chonbuk, South Korea
[2] Wonkwang Univ, Sch Med, Dept Microbiol, Iksan 570749, Chonbuk, South Korea
[3] Wonkwang Univ, Med Resources Res Ctr, Iksan 570749, Chonbuk, South Korea
[4] LG Biotech Inst, Taejeon 305380, South Korea
[5] Chonnam Natl Univ, Sch Med, Dept Surg, Kwangju 500757, South Korea
关键词
nitric oxide; superoxide; Spiraea prunifolia var; simpliciflora;
D O I
10.1016/S0378-8741(99)00101-4
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
It is well established that nitric oxide (NO) and superoxide radicals play pivotal roles in the pathogenesis of inflammatory diseases and fever. This study is undertaken to address whether the methanol extract of Spiraea prunifolia var. simpliciflora root, a traditional medicine as an antipyretic, modulates the generation of NO and superoxide in IFN-gamma primed or polymyristic acetate (PMA) stimulated RAW 264.7 cells, respectively. The generation of NO as well as the expression of inducible nitric oxide synthase (iNOS) protein from IFN-gamma primed RAW 264.7 cells is markedly decreased by the methanol extract in a dose dependent manner. However, the methanol extract does not affect the viability of RAW 264.7 cells, as assessed by methylthiazol-2-yl-2,5-diphenyl tetrazolium bromide (MTT) assay. In addition, the methanol extract suppresses the generation of superoxide in PMA-stimulated RAW 264.7 cells in a dose and a time dependent manner. Taken together, anti-pyretic effects of Spiraea prunifolia var. simpliciflora root extract could result from direct suppression of NO and decreased superoxide generation. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:209 / 217
页数:9
相关论文
共 26 条
[1]
THE CELL BIOLOGY OF MACROPHAGE ACTIVATION [J].
ADAMS, DO ;
HAMILTON, TA .
ANNUAL REVIEW OF IMMUNOLOGY, 1984, 2 :283-318
[2]
ASSEMBLY AND REGULATION OF NADPH OXIDASE AND NITRIC-OXIDE SYNTHASE [J].
BASTIAN, NR ;
HIBBS, JB .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (01) :131-139
[3]
Dinarello CA, 1997, SEMIN ONCOL, V24, P288
[4]
MODULATION OF ADJUVANT ARTHRITIS BY ENDOGENOUS NITRIC-OXIDE [J].
IALENTI, A ;
MONCADA, S ;
DIROSA, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (02) :701-706
[5]
JUN CD, 1994, J IMMUNOL, V153, P3684
[6]
Dexamethasone administered into organum vasculosum laminae terminalis of rabbits induced antipyresis via inhibiting nitric oxide pathway in situ [J].
Lin, MT ;
Lin, JH ;
Yang, YL .
NEUROSCIENCE LETTERS, 1997, 230 (01) :53-56
[7]
SUPPRESSION OF ARTHRITIS BY AN INHIBITOR OF NITRIC-OXIDE SYNTHASE [J].
MCCARTNEYFRANCIS, N ;
ALLEN, JB ;
MIZEL, DE ;
ALBINA, JE ;
XIE, QW ;
NATHAN, CF ;
WAHL, SM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (02) :749-754
[8]
INCREASED NITRIC-OXIDE SYNTHESIS IN ULCERATIVE-COLITIS [J].
MIDDLETON, SJ ;
SHORTHOUSE, M ;
HUNTER, JO .
LANCET, 1993, 341 (8843) :465-466
[9]
Priming of NADPH oxidase by tumor necrosis factor alpha in patients with inflammatory and autoimmune rheumatic diseases [J].
Miesel, R ;
Hartung, R ;
Kroeger, H .
INFLAMMATION, 1996, 20 (04) :427-438
[10]
MILLER MJS, 1993, J PHARMACOL EXP THER, V264, P11