Flavonoids from Cleome droserifolia suppress NO production in activated macrophages in vitro

被引:35
作者
Fushiya, S
Kishi, Y
Hattori, K
Batkhuu, J
Takano, F
Singab, ANB
Okuyama, T
机构
[1] Tohoku Univ, Fac Pharmaceut Sci, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Al Azhar Univ, Fac Pharm, Dept Pharmacognosy, Cairo, Egypt
[3] Meiji Pharmaceut Univ, Tokyo, Japan
关键词
Cleome droserifolia; Capparidaceae; flavonoid; nitric oxide; inflammation; macrophage;
D O I
10.1055/s-1999-14084
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The effect of an Egyptian medicinal plant, Cleome droserifolia (Forssk.) Del. on nitric oxide (NO) production in bacillus Calmette-Guerin-induced mouse peritoneal macrophages activated by lipopolysaccharide was investigated in vitro. The methanol extract of C. droserifolia reduced the NO production, and two flavonoids were isolated as the active components. The new one was determined to be 5,4'-dihydroxy-6,7,8,3',5'-pentamethoxyflavone (1) and the other was identified as 5,4'-dihydroxy-6,7,8,3'-tetramethoxyflavone (8-methoxycirsilineol; 2). Compound 1 concentration-dependently suppressed the NO production and was effective at a non-toxic concentration (12.5 mu g/ml). The suppressive activity of 2 was weaker than that of 1.
引用
收藏
页码:404 / 407
页数:4
相关论文
共 24 条
[1]  
Bellingan GJ, 1996, J IMMUNOL, V157, P2577
[2]   NITRIC-OXIDE - A PHYSIOLOGICAL MESSENGER MOLECULE [J].
BREDT, DS ;
SNYDER, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1994, 63 :175-195
[3]   HEPATOCYTES PRODUCE NITROGEN-OXIDES FROM L-ARGININE IN RESPONSE TO INFLAMMATORY PRODUCTS OF KUPFFER CELLS [J].
CURRAN, RD ;
BILLIAR, TR ;
STUEHR, DJ ;
HOFMANN, K ;
SIMMONS, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (05) :1769-1774
[4]   Inhibition of Kupffer cell functions as an explanation for the hepatoprotective properties of silibinin [J].
Dehmlow, C ;
Erhard, J ;
deGroot, H .
HEPATOLOGY, 1996, 23 (04) :749-754
[5]   GLUCOCORTICOIDS INHIBIT THE INDUCTION OF NITRIC-OXIDE SYNTHASE IN MACROPHAGES [J].
DIROSA, M ;
RADOMSKI, M ;
CARNUCCIO, R ;
MONCADA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 172 (03) :1246-1252
[6]   (+)-rhododendrol and epi-rhododendrin suppress the NO production by activated macrophages in vivo [J].
Fushiya, S ;
Kabe, Y ;
Ikegaya, Y ;
Takano, F .
PLANTA MEDICA, 1998, 64 (07) :598-602
[7]   ANALYSIS OF NITRATE, NITRITE, AND [N-15]-LABELED NITRATE IN BIOLOGICAL-FLUIDS [J].
GREEN, LC ;
WAGNER, DA ;
GLOGOWSKI, J ;
SKIPPER, PL ;
WISHNOK, JS ;
TANNENBAUM, SR .
ANALYTICAL BIOCHEMISTRY, 1982, 126 (01) :131-138
[8]   Timing of prostaglandin exposure is critical for the inhibition of LPS- or IFN-gamma-induced macrophage NO synthesis by PGE(2) [J].
Harbrecht, BG ;
Kim, YM ;
Wirant, EA ;
Simmons, RL ;
Billiar, TR .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 61 (06) :712-720
[9]  
KhairElDin TA, 1996, AM J REPROD IMMUNOL, V36, P1
[10]   ANTIINFLAMMATORY GLUCOCORTICOIDS INHIBIT THE INDUCTION BY ENDOTOXIN OF NITRIC-OXIDE SYNTHASE IN THE LUNG, LIVER AND AORTA OF THE RAT [J].
KNOWLES, RG ;
SALTER, M ;
BROOKS, SL ;
MONCADA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 172 (03) :1042-1048