Gastroprotective effect and cytotoxicity of semisynthetic jatropholone derivatives

Pertino, M; Schmeda-Hirschmann, G; Rodriguez JA.; Theoduloz, C

Abstract

The gastroprotective effect of the diterpenes jatropholone A, jatropholone B and 16 semisynthetic derivatives was assessed in the HCl/ethanol-induced gastric lesion model in mice and the cytotoxicity was determined towards fibroblasts and AGS cells. In a dose-response study, jatropholone B reduced gastric lesions by 65% at 6 mg/kg and jatropholone A by 54% at 100 mg/kg. The jatropholone B derivatives 9-14 and the compounds 15-18 were compared at a single oral dose of 25 mg/kg while the jatropholone A derivatives 2-7 were assessed at 100 mg/kg. A decrease in gastroprotective activity was observed for the ether as well as for the ester derivatives of jatropholone B. The methyl and propyl ethers of jatropholone A were more gastroprotective than the natural product. The placement of an additional methyl group at C-2 in the jatropholone B derivatives led to a loss of selectivity, the methyl and propyl ethers lack a gastroprotective effect. Jatropholone B was not toxic towards AGS cells and fibroblasts. Jatro-pholone A was active only against AGS cells. The gastroprotective effect of the epimeric jatropholones was selective showing a higher effect for jatropholone B. These results further support that the stereochemistry of the methyl group at C-2 in the jatropholones plays a relevant role in preventing the gastric lesions in mice. The compounds 3, 5 - 7, 10 and 12-18 are described for the first time. © Georg Thieme Verlag KG Stuttgart.

Más información

Título según WOS: Gastroprotective effect and cytotoxicity of semisynthetic jatropholone derivatives
Título según SCOPUS: Gastroprotective effect and cytotoxicity of semisynthetic jatropholone derivatives
Título de la Revista: PLANTA MEDICA
Volumen: 73
Número: 10
Editorial: GEORG THIEME VERLAG KG
Fecha de publicación: 2007
Página de inicio: 1095
Página final: 1100
Idioma: English
URL: http://www.thieme-connect.de/DOI/DOI?10.1055/s-2007-981580
DOI:

10.1055/s-2007-981580

Notas: ISI, SCOPUS