Gastroprotective activity of isopulegol on experimentally induced gastric lesions in mice: investigation of possible mechanisms of action

被引:55
作者
Gomes Silva, Maria Izabel [1 ]
Moura, Brinell Arcanjo [1 ]
de Aquino Neto, Manuel Rufino [1 ]
Tome, Adriana da Rocha [2 ]
Moura Rocha, Nayrton Flavio [1 ]
Rodrigues de Carvalho, Alyne Mara [1 ]
Macedo, Danielle Silveira [1 ]
Mendes Vasconcelos, Silvania Maria [1 ]
de Sousa, Damiao Pergentino [3 ]
de Barros Viana, Glauce Socorro [1 ]
Florenco de Sousa, Francisca Clea [1 ]
机构
[1] Univ Fed Ceara, Dept Physiol & Pharmacol, Fac Med, BR-60431270 Fortaleza, Ceara, Brazil
[2] Univ Estadual Ceara, Fac Vet Med, BR-60740903 Fortaleza, Ceara, Brazil
[3] Univ Fed Sergipe, Dept Physiol, BR-49100000 Sergipe, Brazil
关键词
Antiulcerogenic activity; Isopulegol; Monoterpene; Action mechanisms; INDOMETHACIN-INDUCED GASTROPATHY; SENSITIVE POTASSIUM CHANNELS; NEES MEZ LAURACEAE; MUCOSAL LESIONS; NITRIC-OXIDE; ULCEROGENIC ACTIVITY; ESSENTIAL OILS; PANAX-GINSENG; RAT STOMACH; INJURY;
D O I
10.1007/s00210-009-0429-5
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The present study investigated whether isopulegol, a monoterpene present in essential oils of several aromatic plants, would be able to promote some gastroprotective effect and also verified the possible mechanisms involved in this action. For this study, ethanol- and indomethacin-induced gastric ulcer models in mice and histopathological assessment were used. The roles of NO, sulfhydryls (glutathione, GSH), ATP-sensitive K+ channels (K-ATP channels), and prostaglandins were also investigated. Isopulegol exhibited a dose-related gastroprotective effect against ethanol-induced lesions, while the pretreatment with glibenclamide and indomethacin [but not with N(G)-nitro-l-arginine methyl ester] were able to reverse this action. The pretreatment with isopulegol also restored GSH levels to normal levels and exhibited dose-related gastroprotective effect against indomethacin-induced ulcer. The results suggested that isopulegol presents significant gastroprotective effects in both ethanol- and indomethacin-induced ulcer models, which appear to be mediated, at least in part, by endogenous prostaglandins, K-ATP channel opening, and antioxidant properties.
引用
收藏
页码:233 / 245
页数:13
相关论文
共 66 条
[1]
Adeyemi EO, 2005, WORLD J GASTROENTERO, V11, P4154
[2]
Plants with central analgesic activity [J].
Almeida, RN ;
Navarro, DS ;
Barbosa, JM .
PHYTOMEDICINE, 2001, 8 (04) :310-322
[3]
MECHANISM OF ULCEROGENIC ACTIVITY OF INDOMETHACIN AND OXYPHENBUTAZONE [J].
BHARGAVA, KP ;
GUPTA, MB ;
TANGRI, KK .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1973, 22 (02) :191-195
[4]
Fragrance material review on isopulegol [J].
Bhatia, S. P. ;
McGinty, D. ;
Letizia, C. S. ;
Api, A. M. .
FOOD AND CHEMICAL TOXICOLOGY, 2008, 46 (11) :S185-S189
[5]
Grapefruit-seed extract attenuates ethanol-and stress-induced gastric lesions via activation of prostaglandin, nitric oxide and sensory nerve pathways [J].
Brzozowski, Tomasz ;
Konturek, Peter C. ;
Drozdowicz, Danuta ;
Konturek, Stanislaw J. ;
Zayachivska, Oxana ;
Pajdo, Robert ;
Kwiecien, Slawomir ;
Pawlik, Wieslaw W. ;
Hahn, Eckhart G. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2005, 11 (41) :6450-6458
[6]
A comparative study on the activity of lansoprazole, omeprazole and PD-136450 on acidified ethanol- and indomethacin-induced gastric lesions in the rat [J].
Chandranath, SI ;
Bastaki, SMA ;
Singh, J .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2002, 29 (03) :173-180
[7]
Cyclisation of citronellal to isopulegol catalysed by hydrous zirconia and other solid acids [J].
Chuah, GK ;
Liu, SH ;
Jaenicke, S ;
Harrison, LJ .
JOURNAL OF CATALYSIS, 2001, 200 (02) :352-359
[8]
Evaluation of the antiulcerogenic activity of Maytenus robusta (Celastraceae) in different experimental ulcer models [J].
de Andrade, Sergio Faloni ;
Lemos, Marivane ;
Comunello, Eros ;
Noldin, Vania Floriani ;
Filho, Valdir Cechinel ;
Niero, Rivaldo .
JOURNAL OF ETHNOPHARMACOLOGY, 2007, 113 (02) :252-257
[9]
Quebrachitol-induced gastroprotection against acute gastric lesions:: Role of prostaglandins, nitric oxide and K+ATP channels [J].
de Olinda, T. M. ;
Lemos, T. L. G. ;
Machado, L. L. ;
Rao, V. S. ;
Santos, F. A. .
PHYTOMEDICINE, 2008, 15 (05) :327-333
[10]
de Sousa DP, 2007, Z NATURFORSCH C, V62, P563