Título :	Phylloseptin-1 is leishmanicidal for amastigotes of Leishmania amazonensis inside infected macrophages
Autor :	Kückelhaus, Selma Aparecida Souza Aquino, Daniela Sant’Ana de Borges, Tatiana Karla dos Santos Moreira, Daniel Carneiro Leite, Luciana de Magalhães Junqueira, Maria Imaculada Muniz Barboza Kückelhaus, Carlos S. Romero, Gustavo Adolfo Sierra Prates, Maura Vianna Bloch Júnior, Carlos Leite, José Roberto de Souza de Almeida
metadata.dc.identifier.orcid:	https://orcid.org/0000-0002-6813-6276 https://orcid.org/0000-0003-1961-7281 https://orcid.org/0000-0002-6463-362X https://orcid.org/0000-0002-9006-4619 https://orcid.org/0000-0003-1425-926X https://orcid.org/0000-0003-2799-6883 https://orcid.org/0000-0002-1096-3236
Assunto::	Peptídeos antimicrobianos Citocinas Leishmaniose Stress oxidativo
Fecha de publicación :	6-jul-2020
Editorial :	MDPI
Citación :	KÜCKELHAUS, Selma A. S. et al. Phylloseptin-1 is leishmanicidal for amastigotes of Leishmania amazonensis inside infected macrophages. International Journal of Environmental Research and Public Health, v. 17, n. 13, 4856, 2020. DOI:10.3390/ijerph17134856. Disponível em: https://www.mdpi.com/1660-4601/17/13/4856/html. Acesso em: 19 out. 2020.
Abstract:	Leishmania protozoans are the causal agents of neglected diseases that represent an important public health issue worldwide. The growing occurrence of drug-resistant strains of Leishmania and severe side effects of available treatments represent an important challenge for the leishmaniases treatment. We have previously reported the leishmanicidal activity of phylloseptin-1 (PSN-1), a peptide found in the skin secretion of Phyllomedusa azurea (=Pithecopus azureus), against Leishmania amazonensis promastigotes. However, its impact on the amastigote form of L. amazonensis and its impact on infected macrophages are unknown. In this work, we evaluated the effects of PSN-1 on amastigotes of L. amazonensis inside macrophages infected in vitro. We assessed the production of hydrogen peroxide and nitric oxide, as well as the levels of inflammatory and immunomodulatory markers (TGF-β, TNF-α and IL-12), in infected and non-infected macrophages treated with PSN-1. Treatment with PSN-1 decreased the number of infected cells and the number of ingested amastigotes per cell when compared with the untreated cells. At 32 µM (64 µg/mL), PSN-1 reduced hydrogen peroxide levels in both infected and uninfected macrophages, whereas it had little effect on NO production or TGF-β release. The effect of PSN-1 on IL-12 and TNF-α secretion depended on its concentration, but, in general, their levels tended to increase as PSN-1 concentration increased. Further in vitro and in vivo studies are needed to clarify the mechanisms of action of PSN-1 and its interaction with the immune system aiming to develop pharmacological applications.
metadata.dc.description.unidade:	Faculdade de Medicina (FMD)
Licença::	© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
DOI:	https://doi.org/10.3390/ijerph17134856
Aparece en las colecciones:	Artigos publicados em periódicos e afins

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