Gastroprotection of Calein D against Ethanol-Induced Gastric Lesions in Mice: Role of Prostaglandins, Nitric Oxide and Sulfhydryls
María Elena Sánchez-Mendoza,
Yaraset López-Lorenzo,
Leticia Cruz-Antonio,
Audifás-Salvador Matus-Meza,
Yolanda Sánchez-Mendoza,
Jesús Arrieta
Affiliations
María Elena Sánchez-Mendoza
Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón, Colonia Santo Tomás, Delegación Miguel Hidalgo, Ciudad de México 11340, Mexico
Yaraset López-Lorenzo
Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón, Colonia Santo Tomás, Delegación Miguel Hidalgo, Ciudad de México 11340, Mexico
Leticia Cruz-Antonio
Facultad de Estudios Superiores Zaragoza, UNAM. Av. Guelatao No. 66, Colonia Ejército de Oriente Iztapalapa, Ciudad de México 09230, Mexico
Audifás-Salvador Matus-Meza
Departamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico
Yolanda Sánchez-Mendoza
Unidad de Medicina Familiar No. 49, Instituto Mexicano del Seguro Social, Ciudad de México 06600, Mexico
Jesús Arrieta
Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón, Colonia Santo Tomás, Delegación Miguel Hidalgo, Ciudad de México 11340, Mexico
Peptic ulcers are currently treated with various drugs, all having serious side effects. The aim of this study was to evaluate the gastroprotective activity of calein D (from Calea urticifolia), a sesquiterpene lactone with a germacrane skeleton. Gastric lesions were induced in mice by administering ethanol (0.2 mL) after oral treatment with calein D at 3, 10 and 30 mg/kg, resulting in 13.15 ± 3.44%, 77.65 ± 7.38% and 95.76 ± 2.18% gastroprotection, respectively, to be compared with that of the control group. The effect found for 30 mg/kg of calein D was not reversed by pretreatment with NG-nitro-l-arginine methyl ester (l-NAME, 70 mg/kg, ip), indomethacin (10 mg/kg, sc) or N-ethylmaleimide (NEM, 10 mg/kg, sc). Hence, the mechanism of action of calein D does not involve NO, prostaglandins or sulfhydryl compounds. Calein D was more potent than carbenoxolone, the reference drug. The findings for the latter are in agreement with previous reports.