Piperine, quercetin, and curcumin identifed as promising natural products for topical treatment of cutaneous leishmaniasis

ABSTRACT: Leishmania braziliensis (L. braziliensis) causes cutaneous leishmaniasis (CL) in the New World. The costs and the side efects of current treatments render imperative the development of new therapies that are afordable and easy to administer. Topical treatment would be the ideal option for the treatment of CL. This underscores the urgent need for afordable and efective treatments, with natural compounds being explored as potential solutions. The alkaloid piperine (PIP), the polyphenol curcumin (CUR), and the favonoid quercetin (QUE), known for their diverse biological properties, are promising candidates to address these parasitic diseases. Initially, the in vitro cytotoxicity activity of the compounds was evaluated using U-937 cells, followed by the assessment of the leishmanicidal activity of these compounds against amastigotes of L. braziliensis. Subsequently, a golden hamster model with stationary-phase L. braziliensis promastigote infections was employed. Once the ulcer appeared, hamsters were treated with QUE, PIP, or CUR formulations and compared to the control group treated with meglumine antimoniate administered intralesionally. We observed that the three organic compounds showed high in vitro leishmanicidal activity with efective concentrations of less than 50 mM, with PIP having the highest activity at a concentration of 8 mM. None of the compounds showed cytotoxic activity for U937 macrophages with values between 500 and 700 mM. In vivo, topical treatment with QUE daily for 15 days produced cured in 100% of hamsters while the efectiveness of CUR and PIP was 83% and 67%, respectively. No failures were observed with QUE. Collectively, our data suggest that topical formulations mainly for QUE but also for CUR and PIP could be a promising topical treatment for CL. Not only the ease of obtaining or synthesizing the organic compounds evaluated in this work but also their commercial availability eliminates one of the most important barriers or bottlenecks in drug development, thus facilitating the roadmap for the development of a topical drug for the management of CL caused by L. braziliensis

• Autores: Murillo Arroyave, Javier Darío; Arbeláez Córdoba, Natalia; Robledo Restrepo, Sara María; Clemente, Camila Mara; Garro, Ariel G.; Pineda, Tatiana; Ravetti, Soledad
• Tipo de recurso: Article of investigation
• Fecha de publicación: 2024
• Institución: Universidad de Antioquia
• Repositorio: Repositorio UdeA
• Idioma: eng
• OAI Identifier: oai:bibliotecadigital.udea.edu.co:10495/40809
• Acceso en línea: https://hdl.handle.net/10495/40809
• Palabra clave: Alkaloids; Alcaloides; Antiprotozoarios; Antiprotozoal Agents; Benzodioxoles; Cricetinae; Curcumina; Curcumin; Leishmania braziliensis; Leishmaniasis; Mesocricetus; Piperidinas; Piperidines; Alcamidas Poliinsaturadas; Polyunsaturated Alkamides; Quercetina; Quercetin; Leishmaniasis Cutánea; Leishmaniasis, Cutaneous; https://id.nlm.nih.gov/mesh/D000470; https://id.nlm.nih.gov/mesh/D000981; https://id.nlm.nih.gov/mesh/D052117; https://id.nlm.nih.gov/mesh/D006224; https://id.nlm.nih.gov/mesh/D003474; https://id.nlm.nih.gov/mesh/D007892; https://id.nlm.nih.gov/mesh/D007896; https://id.nlm.nih.gov/mesh/D008647; https://id.nlm.nih.gov/mesh/D010880; https://id.nlm.nih.gov/mesh/D053284; https://id.nlm.nih.gov/mesh/D011794; https://id.nlm.nih.gov/mesh/D016773
• Rights: openAccess
• License: http://creativecommons.org/licenses/by/2.5/co/