Glucantime resistant Leishmania promastigotes are sensitive to pentostam.

Abstract

Growth inhibition in vitro tests were used to study the susceptibility to pentostam of different Leishmania strains involved in cutaneous and mucocutaneous leishmaniasis--one glucantime sensitive strain, three naturally glucantime resistant strains and one glucantime resistant line developed by in vitro drug exposure. Contrasting with the high degree of glucantime resistance, all strains were sensitive to pentostam. These differences suggest that there is some relationship between chemical structure and in vitro activity for these antimonial compounds. These data justify a clinical re-evaluation to compare therapeutic efficacy of glucantime and pentostam in the treatment of leishmaniasis.

• Authors: E S Moreira, J B Guerra, M de L Petrillo-Peixoto
• Journal: Revista da Sociedade Brasileira de Medicina Tropical (Rev Soc Bras Med Trop) 1992 Oct-Dec Vol. 25 Issue 4 Pg. 247-50 ISSN: 0037-8682 [Print] Brazil
• PMID: 1340539 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antiprotozoal Agents
• Organometallic Compounds
• Meglumine
• Meglumine Antimoniate
• Antimony
• Antimony Sodium Gluconate

Topics

• Animals
• Antimony (antagonists & inhibitors)
• Antimony Sodium Gluconate (pharmacology)
• Antiprotozoal Agents (antagonists & inhibitors)
• Dose-Response Relationship, Drug
• Drug Resistance
• Leishmania (drug effects, growth & development)
• Leishmania braziliensis (drug effects, growth & development)
• Leishmania guyanensis (drug effects, growth & development)
• Meglumine (antagonists & inhibitors)
• Meglumine Antimoniate
• Organometallic Compounds (antagonists & inhibitors)
• Species Specificity