2003
DOI: 10.1590/s0037-86822003000400018
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Ineficácia in vivo da terbinafina em leishmaniose cutânea causada por Leishmania (Leishmania) amazonensis em camundongos C57BL/6

Abstract: The efficiency of terbinafine was tested in C57BL/6 mice inoculated with the Leishmania (Leishmania) amazonensis strain MHOM/BR/PH8. The mice were administered: terbinafine at a dose of 100mg/kg/d by via oral; 0.9% saline solution orally as the control; and subcutaneous sodium stibogluconate 400mg SbV/kg/d as gold standard, for 20 days. Terbinafine was demonstrated to be ineffective when compared to the controls, using clinical and parasitological parameters and the limiting dilution assay.

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Cited by 7 publications
(2 citation statements)
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“…Among these diseases, cutaneous leishmaniasis (CL) is particularly important in South America because of its chronicity, latency, and the potential to develop metastases that can lead to disfiguring lesions. Chemotherapy with pentavalent antimonial compounds is extensively used to treat this illness; however, its adverse effects, such as parenteral administration, extended treatment regimens, and the appearance of resistance warrant a search for alternative drugs that can be more 10,21 effective .…”
Section: Introductionmentioning
confidence: 99%
“…Among these diseases, cutaneous leishmaniasis (CL) is particularly important in South America because of its chronicity, latency, and the potential to develop metastases that can lead to disfiguring lesions. Chemotherapy with pentavalent antimonial compounds is extensively used to treat this illness; however, its adverse effects, such as parenteral administration, extended treatment regimens, and the appearance of resistance warrant a search for alternative drugs that can be more 10,21 effective .…”
Section: Introductionmentioning
confidence: 99%
“…A controversial result was observed in experimental models of cutaneous leishmaniasis, the treatment with terbinafine of L. major-innfected BALB/c mice was effective in reducing lesions, while in the model L. amazonensis-infected C57Bl/6 mice, this drug led to no significant reduction of both lesion size or parasite load when compared to the untreated control group (48,49). In the in vivo models of visceral infection, treatment of hamsters infected with L. infantum chagasi with terbinafine did not cause a difference in weight or spleen parasite load compared to the untreated control, with a significant decrease only observed when the drug was associated with glucantime (50,51).…”
Section: Antifungalsmentioning
confidence: 98%