Analgesic activity of di-caffeoylquinic acids from roots of Lychnophora ericoides (Arnica da serra)

被引:50
作者
dos Santos, MD
Gobbo-Neto, L
Albarella, L
de Souza, GEP
Lopes, NP
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Quim & Fis, BR-14040903 Ribeirao Preto, SP, Brazil
[2] Univ Salerno, Fac Farm, Dipartimento Sci Farmaceut, I-84084 Fisciano, SA, Italy
基金
巴西圣保罗研究基金会;
关键词
Lychnophora ericoides; Asteraceae; analgesic; roots; di-caffeoylquinic acids;
D O I
10.1016/j.jep.2004.09.043
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The Brazilian medicinal plant Lychnophora ericoides Mart. (Asteraceae) has been used in traditional medicine to treat wounds, pain and inflammation. As part of our continuing investigation of this commercial phytomedicine, we focused on the polar fractions of the plant, since it is employed as alcoholic and hydroalcoholic preparations. The analgesic bioguided fractionation of the root polar extract yielded 3,5-di-O-[E]-caffeoylquinic acid, 4,5-di-O-[E]-caffcoylquinic acid and 3,4,5-tri-O-[E]-caffeoylquinic acid. The n-butanol fraction and the di-caffeoylquinic acids showed significant analgesic activity in the acetic acid-induced mouse writhing test at low but not at high doses. These findings support, at least in part, the validity of the use of Lychnophora ericoides roots in traditional medicine. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:545 / 549
页数:5
相关论文
共 27 条
[1]   Sesquiterpene lactones, triterpenes and flavones from Lychnophora ericoides and Lychnophora pseudovillosissima [J].
Borella, JC ;
Lopes, JLC ;
Vichnewski, W ;
Cunha, WR ;
Herz, W .
BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 1998, 26 (06) :671-676
[2]   Analgesic activity of the lignans from Lychnophora ericoides [J].
Borsato, MLC ;
Grael, CFF ;
Souza, GEP ;
Lopes, NP .
PHYTOCHEMISTRY, 2000, 55 (07) :809-813
[3]   RELEASE OF PROSTAGLANDINS-E AND PROSTAGLANDINS-F IN AN ALGOGENIC REACTION AND ITS INHIBITION [J].
DERAEDT, R ;
JOUQUEY, S ;
DELEVALLEE, F ;
FLAHAUT, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1980, 61 (01) :17-24
[4]  
DUARTE IDG, 1988, BRAZ J MED BIOL RES, V21, P341
[5]   INTERLEUKIN-1-BETA AS A POTENT HYPERALGESIC AGENT ANTAGONIZED BY A TRIPEPTIDE ANALOG [J].
FERREIRA, SH ;
LORENZETTI, BB ;
BRISTOW, AF ;
POOLE, S .
NATURE, 1988, 334 (6184) :698-701
[6]   BRADYKININ INITIATES CYTOKINE-MEDIATED INFLAMMATORY HYPERALGESIA [J].
FERREIRA, SH ;
LORENZETTI, BB ;
POOLE, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (03) :1227-1231
[7]   STUDIES ON THE ACTIVITIES OF TANNINS AND RELATED-COMPOUNDS .10. EFFECTS OF CAFFEETANNINS AND RELATED-COMPOUNDS ON ARACHIDONATE METABOLISM IN HUMAN POLYMORPHONUCLEAR LEUKOCYTES [J].
KIMURA, Y ;
OKUDA, H ;
OKUDA, T ;
HATANO, T ;
ARICHI, S .
JOURNAL OF NATURAL PRODUCTS, 1987, 50 (03) :392-399
[8]  
KIMURA Y, 1985, CHEM PHARM BULL, V33, P690
[9]  
KOSTER R, 1959, FED PROC, V18, P412
[10]  
LOPES NP, 2001, FAPESP PESQUISA, V64, P42