This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Al-Abdely, H. M.
Right arrow Articles by Melby, P. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Al-Abdely, H. M.
Right arrow Articles by Melby, P. C.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, October 1998, p. 2542-2548, Vol. 42, No. 10
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Efficacies of KY62 against Leishmania amazonensis and Leishmania donovani in Experimental Murine Cutaneous Leishmaniasis and Visceral Leishmaniasis

Hail M. Al-Abdely,1,2,* John R. Graybill,1,2 Rosie Bocanegra,1 Laura Najvar,1 Eleanor Montalbo,1 Steven L. Regen,3 and Peter C. Melby1,2

Division of Infectious Diseases, Department of Medicine, The University of Texas Health Science Center at San Antonio,1 and Audie Murphy Veterans Administration Hospital,2 San Antonio, Texas 78284, and Department of Chemistry, Lehigh University, Bethlehem, Pennsylvania 180153

Received 5 February 1998/Returned for modification 24 March 1998/Accepted 15 July 1998

Current therapy for leishmaniasis is unsatisfactory because parenteral antimonial salts and pentamidine are associated with significant toxicity and failure rates. We examined the efficacy of KY62, a new, water-soluble, polyene antifungal, against cutaneous infection with Leishmania amazonensis and against visceral infection with Leishmania donovani in susceptible BALB/c mice. Mice were infected with L. amazonensis promastigotes in the ear pinna and in the tail and were treated with KY62 or amphotericin B. The cutaneous lesions showed a remarkable response to therapy with KY62 at a dose of 30 mg per kg of body weight per day. At this dose, the efficacy of KY62 was equivalent to or better than that of amphotericin B at 1 to 5 mg/kg/day. Mice infected intravenously with 107 L. donovani promastigotes and treated with KY62 showed a 4-log reduction in the parasite burden in the liver and spleen compared to untreated mice. These studies indicate potent activity of KY62 against experimental cutaneous leishmaniasis caused by L. amazoniensis and against experimental visceral leishmaniasis caused by L. donovani.


* Corresponding author. Mailing address: Division of Infectious Diseases, Department of Medicine, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78284. Phone: (210) 567-4823. Fax: (210) 567-4670. E-mail: abdely{at}uthscsa.edu.


Antimicrobial Agents and Chemotherapy, October 1998, p. 2542-2548, Vol. 42, No. 10
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Ashutosh, , Gupta, S., Ramesh, , Sundar, S., Goyal, N. (2005). Use of Leishmania donovani Field Isolates Expressing the Luciferase Reporter Gene in In Vitro Drug Screening. Antimicrob. Agents Chemother. 49: 3776-3783 [Abstract] [Full Text]  
  • Larabi, M., Yardley, V., Loiseau, P. M., Appel, M., Legrand, P., Gulik, A., Bories, C., Croft, S. L., Barratt, G. (2003). Toxicity and Antileishmanial Activity of a New Stable Lipid Suspension of Amphotericin B. Antimicrob. Agents Chemother. 47: 3774-3779 [Abstract] [Full Text]  
  • Murray, H. W. (2001). Clinical and Experimental Advances in Treatment of Visceral Leishmaniasis. Antimicrob. Agents Chemother. 45: 2185-2197 [Full Text]  
  • Al-Abdely, H. M., Graybill, J. R., Loebenberg, D., Melby, P. C. (1999). Efficacy of the Triazole SCH 56592 against Leishmania amazonensis and Leishmania donovani in Experimental Murine Cutaneous and Visceral Leishmaniases. Antimicrob. Agents Chemother. 43: 2910-2914 [Abstract] [Full Text]  
  • Golenser, J., Frankenburg, S., Ehrenfreund, T., Domb, A. J. (1999). Efficacious Treatment of Experimental Leishmaniasis with Amphotericin B-Arabinogalactan Water-Soluble Derivatives. Antimicrob. Agents Chemother. 43: 2209-2214 [Abstract] [Full Text]