Leishmanicidal Activity and Ultrastructural Changes of Maslinic Acid Isolated from Hyptidendron canum

Author:

Adriana Jesus Jéssica1ORCID,Laurenti Márcia Dalastra1ORCID,Lopes Silva Matheus2,Ghilardi Lago João Henrique2,Domingues Passero Luiz Felipe34ORCID

Affiliation:

1. Laboratory of Pathology of Infectious Diseases (LIM50), Department of Pathology, Medical School of São Paulo University, Av. Dr. Arnaldo, 455. Cerqueira César, SP 01246-903, Brazil

2. Centre of Natural and Human Sciences, Federal University of ABC (UFABC), Santo André 09210-580, Brazil

3. São Paulo State University (UNESP), Institute of Biosciences, São Vicente. Praça Infante Dom Henrique, s/n, São Vicente, SP 11330-900, Brazil

4. São Paulo State University (UNESP), Institute for Advanced Studies of Ocean, São Vicente. João Francisco Bensdorp, 1178, São Vicente, SP 11350-011, Brazil

Abstract

The therapeutic arsenal for the treatment of leishmaniasis is limited and has serious obstacles, such as variable activity, high toxicity, and costs. To overcome such limitations, it becomes urgent to characterize new bioactive molecules. Plants produce and accumulate different classes of bioactive compounds, and these molecules can be studied as a strategy to combat leishmaniasis. The study presented herein evaluated the leishmanicidal effect of maslinic acid isolated from the leaves of Hyptidendron canum (Lamiaceae) and investigated the morphological that occurred on Leishmania (Leishmania) infantum upon treatment. Maslinic acid was active and selective against promastigote and amastigote forms in a dose-dependent manner. Additionally, it was not toxic to peritoneal macrophages isolated from golden hamsters, while miltefosine and amphotericin B showed mild toxicity for macrophages. Morphological changes in promastigotes of L. (L.) infantum treated with maslinic acid were related to cytoplasmic degeneration, intense exocytic activity, and blebbing in the kDNA; disruption of mitochondrial cristae was observed in some parasites. The nucleus of promastigote forms seems to be degraded and the chromatin fragmented, suggesting that maslinic acid triggers programmed cell death. These results indicate that maslinic acid may be an interesting molecule to develop new classes of drugs against leishmaniasis.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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