Antinociceptive and antiedematogenic effects of the hydroalcoholic extract and coumarin from Torresea cearensis Fr. All.

被引:27
作者
Leal, LKAM
Matos, ME
Matos, FJA
Ribeiro, RA
Ferreira, FV
Viana, GSB
机构
[1] FED UNIV CEARA,DEPT PHYSIOL & PHARMACOL,BR-60431970 FORTALEZA,CEARA,BRAZIL
[2] FED UNIV CEARA,DEPT PATHOL,BR-60431970 FORTALEZA,CEARA,BRAZIL
关键词
antinociceptive and antiedematogenic activities; Torresea cearensis Fr. All; coumarin;
D O I
10.1016/S0944-7113(97)80071-2
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
This work studied the antinociceptive and antiedematogenic effects of the hydroalcoholic extract (HAE) and coumarin (Coum) from T. cearensis in experimental models of nociception in mice, and carrageenan-and dextran-induced paw edema in rats. HAE (100 and 200 mg/kg, p.o.) and Coum (5-20 mg/kg, p.o.) reduced in a dose-dependent manner the nociception produced by acetic acid and formalin. In the hot plate test, HAE (100-400 mg/kg, p.o.) and Coum (5 and 10 mg/kg, p.o.) increased the latency time to the thermal stimulus 90 min after administration. While naloxone partially reversed the antinociceptive effect of the HAE but not that of Coum, L-arginine reversed the antinociceptive effect of Coum in the formalin test. HAE (200 mg/kg, Po) and Coum (10 and 20 mg/kg, p.o.) significantly inhibited the carrageenan-induced edemas in rats but not the dextran-induced edema. This antiedematogenic effect on the carrageenan model was supported by histological studies performed in sections of the rat paw. In conclusion, the antinociceptive effects of HAE and Coum occur by a mechanism at least in part dependent on the opioid system. The nitric oxide system possibly has also a role in the Coum nociception. In addition, the antiedematogenic activity is manifested in inflammatory processes dependent on polimorphonuclear cells.
引用
收藏
页码:221 / 227
页数:7
相关论文
共 34 条
[1]  
AHERNE W, 1970, Journal of Medical Laboratory Technology, V27, P160
[2]  
BRAGA R, 1976, PLANTAS NORDESTE ESP, P219
[3]  
BUCKLEY TL, 1991, J IMMUNOL, V146, P3424
[4]  
CORREA PM, 1984, DICIONARIO PLANTAS U, V2, P474
[5]  
DERAEDT R, 1976, ARCH INT PHARMACOD T, V224, P30
[6]   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
[7]   STUDIES OF MEDIATORS OF ACUTE INFLAMMATORY RESPONSE INDUCED IN RATS IN DIFFERENT SITES BY CARRAGEENAN AND TURPENTINE [J].
DIROSA, M ;
GIROUD, JP ;
WILLOUGHBY, DA .
JOURNAL OF PATHOLOGY, 1971, 104 (01) :15-+
[8]   PERIPHERAL ANALGESIA AND ACTIVATION OF THE NITRIC OXIDE-CYCLIC GMP PATHWAY [J].
DUARTE, IDG ;
LORENZETTI, BB ;
FERREIRA, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 186 (2-3) :289-293
[9]   ANALGESIA BY DIRECT ANTAGONISM OF NOCICEPTOR SENSITIZATION INVOLVES THE ARGININE-NITRIC OXIDE-CGMP PATHWAY [J].
DUARTE, IDG ;
DOSSANTOS, IR ;
LORENZETTI, BB ;
FERREIRA, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 217 (2-3) :225-227
[10]   PURIFICATION OF SUBUNITS OF ESCHERICHIA-COLI DNA GYRASE AND RECONSTITUTION OF ENZYMATIC-ACTIVITY [J].
HIGGINS, NP ;
PEEBLES, CL ;
SUGINO, A ;
COZZARELLI, NR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (04) :1773-1777