Characterization of the Effect of N-(2-Methoxyphenyl)-1-methyl-1H-benzimidazol-2-amine, Compound 8, against Leishmania mexicana and Its In Vivo Leishmanicidal Activity

Author:

Nieto-Meneses Rocío12,Castillo Rafael3ORCID,Hernández-Campos Alicia3ORCID,Nogueda-Torres Benjamín1ORCID,López-Villegas Edgar Oliver4ORCID,Moreno-Rodríguez Adriana5ORCID,Matadamas-Martínez Félix2,Yépez-Mulia Lilián2ORCID

Affiliation:

1. Departamento de Parasitología, ENCB-Instituto Politécnico Nacional, Mexico City 11340, Mexico

2. Unidad de Investigación Médica en Enfermedades Infecciosas y Parasitarias-UMAE Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City 06720, Mexico

3. Departamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico

4. Central de Microscopia, ENCB-Instituto Politécnico Nacional, Mexico City 11340, Mexico

5. Facultad de Ciencias Químicas, Universidad Autónoma Benito Juárez de Oaxaca, Oaxaca 68120, Mexico

Abstract

Chemotherapy currently available for leishmaniasis treatment has many adverse side effects and drug resistance. Therefore, the identification of new targets and the development of new drugs are urgently needed. Previously, we reported the synthesis of a N-(2-methoxyphenyl)-1-methyl-1H-benzimidazol-2-amine, named compound 8, with an IC50 value in the micromolar range against L. mexicana, it also inhibited 68.27% the activity of recombinant L. mexicana arginase. Herein, we report studies carried out to characterize the mechanism of action of compound 8, as well as its in vivo leishmanicidal activity. It was shown in our ultrastructural studies that compound 8 induces several changes, such as membrane blebbing, the presence of autophagosomes, membrane detachment and mitochondrial and kinetoplast disorganization, among others. Compound 8 triggers the production of ROS and parasite apoptosis. It reduced 71% of the parasite load of L. mexicana in an experimental model of cutaneous leishmaniasis in comparison with a control. Altogether, the data obtained suggest the potential use of compound 8 in the treatment of cutaneous leishmaniasis.

Funder

Instituto Mexicano del Seguro Social

Publisher

MDPI AG

Reference32 articles.

1. (2023, November 28). Word Health Organization: Leishmaniasis [Updated 2023 Jan 12]. Available online: https://www.who.int/news-room/fact-sheets/detail/leishmaniasis.

2. (2023, November 28). Pan American Health Organization: Leishmaniasis. Available online: https://www.paho.org/en/topics/leishmaniasis.

3. Pan American Health Organization (2023, November 22). Leishmaniasis: Epidemiological Report for the Americas. No. 11 (December 2022). Available online: https://iris.paho.org/bitstream/handle/10665.2/56831.

4. Choi, H.L., Jain, S., Ruiz Postigo, J.A., Borisch, B., and Dagne, D.A. (2021). The global procurement landscape of leishmaniasis medicines. PLoS Negl. Trop. Dis., 15.

5. Comparison between systemic and intralesional meglumine antimoniate therapy in a primary health care unit;Soares;Acta Trop.,2019

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