Inhibitory effect of Ginkgo biloba extract on the expression of inducible nitric oxide synthase in endothelial cells

被引:57
作者
Cheung, F
Siow, YL
Chen, WZ
O, K
机构
[1] Univ Hong Kong, Fac Med, Dept Pharmacol, Hong Kong, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 200031, Peoples R China
关键词
nitric oxide; endothelial cells; Ginkgo biloba leaf extracts;
D O I
10.1016/S0006-2952(99)00255-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Excessive production of nitric oxide (NO) may have cytotoxic effects through the formation of peroxynitrite with superoxide. The extract of Ginkgo biloba leaves (EGb) has been demonstrated to be a potent scavenger of free radicals. Although EGb has been shown recently to inhibit NO production in macrophages, its effect on NO production in endothelial cells is largely unknown. The objective of this study was to elucidate the mechanism by which EGb affects NO production in a human endothelial cell line (EGV304). After cells were incubated with EGb (10-100 mu g/mL) for 2 or 4 hr, the amounts of NO metabolites released by the cells were quantitated, and cellular NOS activities were determined following the conversion of [H-3]arginine to [H-3]citrulline. NOS protein expression was determined by western immunoblotting analysis. mRNA levels were examined by reverse transcription-polymerase chain reaction (RT-PCR) analysis. EGb (50 mu g/mL) caused a 30% reduction of NO metabolites released by endothelial cells. Following EGb treatment, cellular inducible NO synthase (iNOS) activity was reduced by 28% with a concomitant reduction in the levels of iNOS protein mass and mRNA. There was no change in the activity or protein mass of constitutive NO synthase in these cells. EGb inhibited NO production by attenuating the level of iNOS mRNA in ECV304 cells. Selective inhibition of iNOS by EGb may be therapeutically relevant in modulating NO production in endothelial cells. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:1665 / 1673
页数:9
相关论文
共 49 条
[31]   Inducible nitric oxide synthase: What difference does it make? [J].
Nathan, C .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (10) :2417-2423
[32]  
NATHAN C, 1994, J BIOL CHEM, V269, P13725
[33]  
O K, 1995, J LIPID RES, V36, P2344
[34]   HYPERCHOLESTEROLEMIA INCREASES ENDOTHELIAL SUPEROXIDE ANION PRODUCTION [J].
OHARA, Y ;
PETERSON, TE ;
HARRISON, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2546-2551
[35]   Ginkgo biloba extract protects brain neurons against oxidative stress induced by hydrogen peroxide [J].
Oyama, Y ;
Chikahisa, L ;
Ueha, T ;
Kanemaru, K ;
Noda, K .
BRAIN RESEARCH, 1996, 712 (02) :349-352
[36]   Therapeutic strategies for the inhibition of inducible nitric oxide synthase - Potential for a novel class of anti-inflammatory agents [J].
Pfeilschifter, J ;
Eberhardt, W ;
Hummel, R ;
Kunz, D ;
Muhl, H ;
Nitsch, D ;
Pluss, C ;
Walker, G .
CELL BIOLOGY INTERNATIONAL, 1996, 20 (01) :51-58
[37]   Ginkgo biloba attenuates oxidative stress in macrophages and endothelial cells [J].
Rong, YG ;
Geng, ZH ;
Lau, BHS .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (01) :121-127
[38]   Effects of EGb 761 on nitric oxide and oxygen free radicals, myocardial damage and arrhythmia in ischemia-reperfusion injury in vivo [J].
Shen, JG ;
Wang, J ;
Zhao, BL ;
Hou, JW ;
Gao, TL ;
Xin, WJ .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1998, 1406 (03) :228-236
[39]   INDUCIBLE NITRIC-OXIDE SYNTHASE MESSENGER-RNA AND ACTIVITY IN GLOMERULAR MESANGIAL CELLS [J].
SHULTZ, PJ ;
ARCHER, SL ;
ROSENBERG, ME .
KIDNEY INTERNATIONAL, 1994, 46 (03) :683-689
[40]   MAMMALIAN NITRATE BIOSYNTHESIS - MOUSE MACROPHAGES PRODUCE NITRITE AND NITRATE IN RESPONSE TO ESCHERICHIA-COLI LIPOPOLYSACCHARIDE [J].
STUEHR, DJ ;
MARLETTA, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (22) :7738-7742