Planta Med 2009; 75(2): 148-151
DOI: 10.1055/s-0028-1088347
Pharmacology
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Modulation of Macrophage Functions by Compounds Isolated from Zingiber officinale

Eun Mi Koh1 , Hye Jin Kim2 , Sohee Kim1 , Woo Hyuck Choi1 , Yeon Hee Choi2 , Shi Yong Ryu2 , Young Sup Kim2 , Woo Suk Koh1 , Shin-Young Park1
  • 1Korea Institute of Toxicology, Daejeon, Korea
  • 2Korea Research Institute of Chemical Technology, Daejeon, Korea
Further Information

Publication History

Received: March 31, 2008 Revised: September 1, 2008

Accepted: October 1, 2008

Publication Date:
24 November 2008 (online)

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Abstract

Bioactivity-guided fractionation of Zingiber officinale (Zingiberaceae) led us to isolate 14 compounds, [4]-gingerol (1), [6]-gingerol (2), [8]-gingerol (3), [10]-gingerol (4), [6]-paradol (5), [4]-shogaol (6), [6]-shogaol (7), 1-dehydro-[10]-gingerdione (8), [10]-gingerdione (9), hexahydrocurcumin (10), tetrahydrocurcumin (11), gingerenone A (12), 1,7-bis-(4’ hydroxyl-3’ methoxyphenyl)-5-methoxyhepthan-3-one (13), and methoxy-[10]-gingerol (14). Using the RAW 264.7 cell line, the inhibitory effects on nitric oxide production induced by lipopolysaccharide and the stimulatory effects on phagocytosis of these compounds were evaluated. Compounds 7, 8, and 9 significantly decreased lipopolysaccharide-induced nitric oxide production, and compounds 7 and 8 significantly reduced inducible nitric oxide synthase expression. Among them, compound 8 also showed significant stimulatory effects on phagocytosis.

Abbreviations

Con A:concanavalin A

DMEM:Dulbecco’s modified Eagle’s medium

FBS:fetal bovine serum

iNOS:inducible nitric oxide synthase

LPS:lipopolysaccharide

NO:nitric oxide

TTBS:Tween tris buffered saline

References

Shin-Young Park, PhD.

Korea Institute of Toxicology

100 Jangdong, Yuseong

Daejeon 305–343

Korea

Phone: +82-42-610-8224

Fax: +82-42-610-8172

Email: sypark@kitox.re.kr