Planta Med 2007; 73(4): 310-317
DOI: 10.1055/s-2007-967153
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Gastroprotective Effect and Cytotoxicity of Labdenamides

Rafael Izquierdo2 , Luis Astudillo2 , Jaime A. Rodríguez3 , Cristina Theoduloz3 , José A. Palenzuela4 , Guillermo Schmeda-Hirschmann1
  • 1Laboratorio de Química de Productos Naturales, Instituto de Química de Recursos Naturales, Universidad de Talca, Talca, Chile
  • 2Laboratorio de Síntesis Orgánica, Instituto de Química de Recursos Naturales, Universidad de Talca, Talca, Chile
  • 3Depto. de Ciencias Básicas Biomédicas, Facultad de Ciencias de la Salud, Universidad de Talca, Talca, Chile
  • 4Centro de Productos Naturales Orgánicos ”Antonio González”, Depto. de Química Orgánica, Facultad de Farmacia, Universidad de La Laguna, Tenerife, Spain
Further Information

Publication History

Received: September 21, 2006 Revised: January 24, 2007

Accepted: February 1, 2007

Publication Date:
05 April 2007 (online)

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Abstract

Some 18 aromatic amides from the labdane diterpenes 15-acetoxyimbricatolic acid and 15-acetoxylabd-8(9)-en-19-oic acid were prepared and assessed for their gastroprotective effect in the HCl/EtOH-induced gastric lesion model in mice. The analysis of the gastroprotective activity of the benzylamides belonging to the series 8(9)- and 8(17)-ene was undertaken at doses of 12.5, 25 and 50 mg/kg in the HCl/EtOH-induced gastric lesion model in mice. A statistically significant gastroprotective effect was observed for 15-acetoxylabd-8(9)-en-19-oic acid benzylamide starting at 12.5 mg/kg, reducing the gastric lesions by 50 %, while 15-acetoxylabd-8(17)-en-19-oic acid benzylamide reduced lesions by 66 % at 25 mg/kg. The 25 mg/kg dose was used for the comparison of the different amides. At 25 mg/kg, the highest gastroprotective effect was observed for the benzyl- and 3-bromophenylamides from 15-acetoxyimbricatolic acid as well as for the benzyl- and p-toluidylamides of 15-acetoxylabd-8(9)-en-19-oic acid, being as active as lansoprazole at 20 mg/kg. Most compounds displayed low toxicity against epithelial gastric (AGS) and human lung fibroblasts cells, with IC50 values > 1000 μM. The highest cytotoxicity towards AGS cells was observed for the 2-bromophenyl- and 2-hydroxy-5-chlorophenylamides in both diterpene series, with IC50 values in the range of 14 - 34 μM towards AGS cells and 10 - 37 μM towards fibroblasts, respectively.