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Activity of compounds isolated from Chilean lichens against experimental cutaneous leishmaniasis.

Abstract
Three secondary metabolites isolated from Chilean lichens, (+) usnic acid, pannarine and 1'-chloropannarine, were tested against promastigotes forms of three strains of Leishmania ssp. Pannarine and 1'-chloropannarine exhibited in vitro activity at 50 micrograms/ml and (+) usnic acid at 25 micrograms/ml. BALB/c mice infected with Leishmania amazonensis were treated 4 weeks post-infection with (+) usnic acid by subcutaneous or oral routes for 15 days at 25 mg/kg or by five intralesional injections at interval of 4 days at 25 mg/kg of body weight. The reference drug, N-methylglucamine antimonate (Glucantime), was administered by subcutaneous injections (regimens of 28 mg of pentavalent antimony) for 15 days. The subcutaneous and oral treatments with (+) usnic did not produce any effect, but by intralesional administration we observed a significant effect that reduced by 43.34% the weight lesions and by 72.28% the parasites loads in infected footpads.
AuthorsA Fournet, M E Ferreira, A Rojas de Arias, S Torres de Ortiz, A Inchausti, G Yaluff, W Quilhot, E Fernandez, M E Hidalgo
JournalComparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology (Comp Biochem Physiol C Pharmacol Toxicol Endocrinol) Vol. 116 Issue 1 Pg. 51-4 (Jan 1997) ISSN: 1367-8280 [Print] United States
PMID9080673 (Publication Type: Journal Article)
Chemical References
  • Antiprotozoal Agents
  • Benzofurans
  • Benzoxepins
  • Depsides
  • usnic acid
  • argopsin
  • pannarin
Topics
  • Animals
  • Antiprotozoal Agents (therapeutic use)
  • Benzofurans (pharmacology, therapeutic use)
  • Benzoxepins (pharmacology, therapeutic use)
  • Depsides
  • Female
  • Leishmaniasis, Cutaneous (drug therapy)
  • Lichens (chemistry)
  • Male
  • Mice
  • Mice, Inbred BALB C

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