Show simple item record

Authordc.contributor.authorDelporte Vergara, Carla 
Authordc.contributor.authorBackhouse Erazo, Nadine es_CL
Authordc.contributor.authorSalinas, P. es_CL
Authordc.contributor.authorSan Martín Barrientos, Aurelio es_CL
Authordc.contributor.authorBórquez, J. es_CL
Authordc.contributor.authorLoyola, A. es_CL
Admission datedc.date.accessioned2009-06-19T17:09:45Z
Available datedc.date.available2009-06-19T17:09:45Z
Publication datedc.date.issued2003-04-03
Cita de ítemdc.identifier.citationBIOORGANIC & MEDICINAL CHEMISTRY 11(7):1187-1190en
Identifierdc.identifier.issn0968-0896
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120680
Abstractdc.description.abstractAzorella compacta, Azorella yareta and Laretia acaulis (Apiaceae) are native species from the high Andes Mountains, northeastern Chile, and they have being traditionally used to treat asthma, colds and bronchitis, illnesses with inflammation and pain as the main symptoms. Interestingly, there are no scientific reports available on their benefits or toxicity. This study was carried out with the purpose of validating the medicinal use of these species and to discover anti-inflammatory and analgesic new molecules. As a working hypothesis, we have proposed that these medicinal species contain bioactive compounds with antiinflammatory and analgesic effects. In this context, azorellanol, 13-hydroxy-7-oxoazorellane and 7-deacetylazorellanol, three diterpenoids previously isolated only from these plants, were subjected to farmaco-toxicological evaluation. Their topical anti-inflammatory and analgesic activities along with acute toxicities or innocuosness were also investigated. Our results indicate the absence of toxic and side effects in mice. All compounds presented dose-related inhibition of pain. 13-hydroxy-7-oxoazorellane was the most potent analgesic but it was less effective than sodium naproxen, the reference drug. Azorellanol exhibited the highest topical antiinflammatory potency on AA (arachidonic acid) and TPA (12-deoxyphorbol 13-tetradecanoate) induced oedema, and it effect was similar to the reference drugs (nimesulide and indomethacin). Probably, its mechanism of action could be explained through the inhibition to cyclo-oxygenase activity. Our results corroborate the anti-inflammatory and analgesic effects of these species, and it justifies their use in folk medicine.en
Lenguagedc.language.isoenen
Publisherdc.publisherPERGAMON-ELSEVIER SCIENCE LTDen
Keywordsdc.subjectARACHIDONIC-ACIDen
Títulodc.titlePharmaco-toxicological study of diterpenoidsen
Document typedc.typeArtículo de revista


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record