Anti-ulcerogenic activity of xanthanolide sesquiterpenes from Xanthium cavanillesii in rats

被引:67
作者
Favier, LS
María, AOM
Wendel, GH
Borkowski, EJ
Giordano, OS
Pelzer, L
Tonn, CE
机构
[1] Univ Nacl San Luis, Fac Quim Bioquim & Farm, Dept Quim, INTEQUI CONICET UNSL, RA-5700 San Luis, Argentina
[2] Univ Nacl San Luis, Fac Quim Bioquim & Farm, Dept Farm, Unidad Farmacol, RA-5700 San Luis, Argentina
关键词
xanthanolides; xanthatin; gastric anti-ulcer activity; gastric; Xanthium cavanillesii;
D O I
10.1016/j.jep.2005.02.042
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The preventive effect of natural xanthanolides as well as a series of synthetic derivatives on ulcer formation induced by absolute ethanol in rats was examined. Among the compounds tested, xanthatin gave the strongest protective activity. The inhibitory action exerted by this molecule on the lesions induced by 0.6N HCl and 0.2N NaOH was highly significant, reducing ulceration in the range of 58-96% at a dose from 12.5 to 100 mg/kg. These results appear to confirm that the presence of a non-hindered alpha,beta-unsaturated carbonyl group seems to be an essential structural requirement for the gastric cytoprotective activity of these compounds. In order to explore this possibility, a theoretical conformational analysis was performed. We suggest that the mechanism of protection would involve, at least in part, a nucleophylic attack of the sulfhydryl group from the biological molecules present in the gastric mucosa to electrophylic carbons accessible in suitable Michael acceptors. (C) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:260 / 267
页数:8
相关论文
共 25 条
[1]   XANTHANOLIDES FROM XANTHIUM-SPINOSUM [J].
ABDEIMOGIB, M ;
DAWIDAR, AM ;
METWALLY, MA ;
ABOUELZAHAB, M .
PHYTOCHEMISTRY, 1991, 30 (10) :3461-3462
[2]  
ALONSO JR, 1998, TRATADO FITOMEDICINA, P386
[3]   Structure - Cytotoxicity relationships of some helenanolide-type sesquiterpene lactones [J].
Beekman, AC ;
Woerdenbag, HJ ;
vanUden, W ;
Pras, N ;
Konings, AWT ;
Wikstrom, HV ;
Schmidt, TJ .
JOURNAL OF NATURAL PRODUCTS, 1997, 60 (03) :252-257
[4]   NATURALLY OCCURRING TERPENE DERIVATIVES .142. NEW SESQUITERPENE LACTONES FROM INULA SPECIES [J].
BOHLMANN, F ;
MAHANTA, PK ;
JAKUPOVIC, J ;
RASTOGI, RC ;
NATU, AA .
PHYTOCHEMISTRY, 1978, 17 (07) :1165-1172
[5]   NATURALLY-OCCURRING TERPENE DERIVATIVES .348. FURTHER EUDESMANOLIDES AND XANTHANOLIDES FROM TELEKIA-SPECIOSA [J].
BOHLMANN, F ;
JAKUPOVIC, J ;
SCHUSTER, A .
PHYTOCHEMISTRY, 1981, 20 (08) :1891-1893
[6]   STRUCTURE ACTIVITY RELATIONSHIP IN THE GASTRIC CYTOPROTECTIVE EFFECT OF SEVERAL SESQUITERPENE LACTONES [J].
GIORDANO, OS ;
PESTCHANKER, MJ ;
GUERREIRO, E ;
SAAD, JR ;
ENRIZ, RD ;
RODRIGUEZ, AM ;
JAUREGUI, EA ;
GUZMAN, J ;
MARIA, AOM ;
WENDEL, GH .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (13) :2452-2458
[7]   MUCUS SYNTHESIS AND SULFHYDRYL-GROUPS IN CYTOPROTECTION MEDIATED BY DEHYDROLEUCODINE, A SESQUITERPENE LACTONE [J].
GUARDIA, T ;
GUZMAN, JA ;
PESTCHANKER, MJ ;
GUERREIRO, E ;
GIORDANO, OS .
JOURNAL OF NATURAL PRODUCTS, 1994, 57 (04) :507-509
[8]   Novel strategies for the discovery of plant-derived anticancer agents [J].
Kinghorn, AD ;
Farnsworth, NR ;
Soejarto, DD ;
Cordell, GA ;
Pezzuto, JM ;
Udeani, GO ;
Wani, MC ;
Wall, ME ;
Navarro, HA ;
Kramer, RA ;
Menendez, AT ;
Fairchild, CR ;
Lane, KE ;
Forenza, S ;
Vyas, DM ;
Lam, KS ;
Shu, YZ .
PURE AND APPLIED CHEMISTRY, 1999, 71 (09) :1611-1618
[9]   Thiazinedione from Xanthium strumarium [J].
Ma, YT ;
Huang, MC ;
Hsu, FL ;
Chang, HF .
PHYTOCHEMISTRY, 1998, 48 (06) :1083-1085
[10]  
MALIK MS, 1993, PHYTOCHEMISTRY, V32, P206, DOI 10.1016/0031-9422(92)80135-2