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Study of therapeutic effect of different concentrations of imatinib on Balb/c model of cutaneous leishmaniasis. | LitMetric

AI Article Synopsis

  • * Imatinib, an anticancer drug known for inhibiting protein kinases, was tested for its effectiveness against CL due to the crucial role of these enzymes in the disease.
  • * In a study using Balb/c mice, imatinib at a dose of 50 mg/kg showed significant improvement in treating CL ulcers compared to a negative control group, indicating its potential as a treatment option.

Article Abstract

Leishmaniasis, as a tropical and subtropical disease, is endemic in more than 90 countries around the world. Today, cutaneous leishmaniasis (CL) that affects more than 1.5 million people per year lacks a definitive treatment approach. Imatinib is an anticancer drug that inhibits the abnormal function of Bcr-Abl due to its tyrosine kinase inhibitor, and that was the reason why the drug was tested for CL treatment because protein kinases are essential enzymes in the genus. In this study, the CL model of Balb/c mice was produced by injection of the cultured metacyclic form of parasite at the base of the tail. The possible recovery of CL ulcers and determination of the optimum dose of imatinib against amastigotes were evaluated. A significant decrease was observed in mice treated with amphotericin B (positive control group) as well as imatinib 50 mg/kg compared to the unreceived drug, negative control group (P<0.05). This study could be promising in gaining insight into the potential of imatinib as an effective treatment approach against CL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326727PMC
http://dx.doi.org/10.3934/microbiol.2020010DOI Listing

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