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DOI 10.1016/j.bcp.2016.12.018

Медицинская библиотека · Biochemical pharmacology · 2016

Antileishmanial activity of verbascoside: Selective arginase inhibition of intracellular amastigotes of Leishmania (Leishmania) amazonensis with resistance induced by LPS plus IFN-γ.

Maquiaveli Claudia do Carmo, Rochetti Arina Lázaro, Fukumasu Heidge, Vieira Paulo Cezar, da Silva Edson Roberto

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Verbascoside is the main component of the traditional medicinal plants that were used against protozoa parasites that cause malaria and leishmaniasis. Previously, we have described verbascoside inhibition of Leishmania amazonensis arginase as well as its antileishmanial action against extracellular promastigotes. In this study, we have assessed arginase parasite inhibition in intracellular amastigotes. In addition, we verified whether verbascoside can influence the host defense against the parasite by measuring gene expression of cytokines IL-1b, IL-10, IL-18, TNF-α and murine macrophage arginase as well as nitric oxide synthase enzymes. Our results show that verbascoside acts on intracellular amastigotes of L. amazonensis (EC50=32μM) by selectively inhibiting the parasite arginase. Verbascoside did not affect the expression of cytokines or enzymes by murine macrophages. However, verbascoside was active against L. (L.) amazonensis amastigotes that were resistant to treatment with LPS and IFN-γ. Verbascoside action on L. amazonensis can be associated with reduction of the protective oxidative mechanism of the parasite leading to impaired trypanothione synthesis that is induced by the parasite arginase inhibition.

Для цитирования: Maquiaveli Claudia do Carmo, Rochetti Arina Lázaro, Fukumasu Heidge, Vieira Paulo Cezar, da Silva Edson Roberto. Antileishmanial activity of verbascoside: Selective arginase inhibition of intracellular amastigotes of Leishmania (Leishmania) amazonensis with resistance induced by LPS plus IFN-γ.. Biochemical pharmacology. 2016. DOI: 10.1016/j.bcp.2016.12.018.

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