Stimulation of nitric oxide synthesis by the aqueous extract of Panax ginseng root in RAW 264.7 cells

被引:54
作者
Friedl, R
Moeslinger, T
Kopp, B
Spieckermann, PG
机构
[1] Inst Physiol, A-1090 Vienna, Austria
[2] Univ Vienna, Ctr Pharm, Inst Pharmacognosy, A-1090 Vienna, Austria
关键词
inducible nitric oxide synthase; Panax ginseng; ginsenosides; food additive; herbal medicine; cell culture;
D O I
10.1038/sj.bjp.0704425
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 In this study, we investigated the effect of Panax ginseng root aqueous extracts upon inducible nitric oxide synthesis in RAW 264.7 cells. Panax ginseng root extract has been used in the Asian world for centuries as a traditional herb to enhance physical strength and resistance and is becoming more and more popular in Europe and North America. 2 Incubation of murine macrophages (RAW 264.7 cells) with increasing amounts of aqueous extracts of Panax ginseng (0.05-0.8 mug mul(-1)) showed a dose dependent stimulation of inducible nitric oxide synthesis. 3 Polysaccharides isolated from Panax ginseng showed strong stimulation of inducible nitric oxide synthesis, whereas a triterpene-enriched fraction from an aqueous extract of Panax ginseng did not show any stimulation. 4 Inducible nitric oxide synthase protein expression was enhanced in a dose dependent manner as revealed by immunoblotting when cells were incubated with increasing amounts of Panax ginseng extract. This was associated with an incline in inducible nitric oxide synthase mRNA-levels as determined by semiquantitative polymerase chain reaction and electromobility shift assay studies indicated enhanced nuclear factor-kappaB DNA binding activity. 5 As nitric oxide plays an important role in immune function, Panax ginseng treatment could modulate several aspects of host defense mechanisms due to stimulation of the inducible nitric oxide synthase.
引用
收藏
页码:1663 / 1670
页数:8
相关论文
共 44 条
[31]   VASCULAR ENDOTHELIAL-CELLS SYNTHESIZE NITRIC-OXIDE FROM L-ARGININE [J].
PALMER, RMJ ;
ASHTON, DS ;
MONCADA, S .
NATURE, 1988, 333 (6174) :664-666
[32]  
Park YC, 1996, BIOCHEM MOL BIOL INT, V40, P751
[33]  
PEREZPEREZ GI, 1995, INFECT IMMUN, V63, P1183
[34]   NITRIC-OXIDE SYNTHASE - MESSENGER-RNA EXPRESSION OF DIFFERENT ISOFORMS IN HUMAN MONOCYTES/MACROPHAGES [J].
REILING, N ;
ULMER, AJ ;
DUCHROW, M ;
ERNST, M ;
FLAD, HD ;
HAUSCHILDT, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (08) :1941-1944
[35]   Mycobacterium tuberculosis (MTB)-stimulated production of nitric oxide by human alveolar macrophages and relationship of nitric oxide production to growth inhibition of MTB [J].
Rich, EA ;
Torres, M ;
Sada, E ;
Finegan, CK ;
Hamilton, BD ;
Toossi, Z .
TUBERCLE AND LUNG DISEASE, 1997, 78 (5-6) :247-255
[36]  
Scaglione F, 1996, DRUG EXP CLIN RES, V22, P65
[37]  
Scaglione F, 1996, DRUG EXP CLIN RES, V22, P338
[38]   INDUCTION AND POTENTIAL BIOLOGICAL RELEVANCE OF A CA2+-INDEPENDENT NITRIC-OXIDE SYNTHASE IN THE MYOCARDIUM [J].
SCHULZ, R ;
NAVA, E ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 105 (03) :575-580
[39]   Ginseng treatment enhances bacterial clearance and decreases lung pathology in athymic rats with chronic P-aeruginosa pneumonia [J].
Song, ZJ ;
Johansen, HK ;
Faber, V ;
Hoiby, N .
APMIS, 1997, 105 (06) :438-444
[40]   Stimulation of interleukin-8 production by acidic polysaccharides from the root of Panax ginseng [J].
Sonoda, Y ;
Kasahara, T ;
Mukaida, N ;
Shimizu, N ;
Tomoda, M ;
Takeda, T .
IMMUNOPHARMACOLOGY, 1998, 38 (03) :287-294