Ursolic acid‐rich extract presents trypanocidal action in vitro but worsens mice under experimental acute Chagas disease

Author:

Daga Maiara A.1,Nicolau Scheila T.1,Jurumenha‐Barreto Juliana1,Lima Lucas B. S.1,Cabral Isaac L.1,Pivotto Ana Paula1,Stefanello Amanda1,Amorim João P. A.2,Hoscheid Jaqueline3,Silva Edson A.4ORCID,Ayala Thaís S.1,Menolli Rafael A.1ORCID

Affiliation:

1. Laboratory of Applied Immunology, Center of Medical and Pharmaceutical Sciences Western Parana State University Cascavel Brazil

2. Center of Biological and Health Sciences Western Parana State University Cascavel Brazil

3. Professional Master's Program in Medicinal Plants and Herbal Medicine in Primary Care Universidade Paranaense Umuarama Brazil

4. Laboratory of Biotechnological Processes and Separation, Center of Exact and Technological Sciences Western Parana State University Toledo Brazil

Abstract

AbstractChagas disease is a neglected tropical disease with only two drugs available for treatment and the plant Cecropia pachystachya has several compounds with antimicrobial and anti‐inflammatory activities. This study aimed to evaluate a supercritical extract from C. pachystachya leaves in vitro and in vivo against Trypanosoma cruzi. A supercritical CO2 extraction was used to obtain the extract (CPE). Cytotoxicity and immunostimulation ability were evaluated in macrophages, and the in vitro trypanocidal activity was evaluated against epimastigotes and trypomastigotes forms. In vivo tests were done by infecting BALB/c mice with blood trypomastigotes forms and treating animals orally with CPE for 10 days. The parasitemia, survival rate, weight, cytokines and nitric oxide dosage were evaluated. CPE demonstrated an effect on the epi and trypomastigotes forms of the parasite (IC50 17.90 ± 1.2 μg/mL; LC50 26.73 ± 1.2 μg/mL) and no changes in macrophages viability, resulting in a selectivity index similar to the reference drug. CPE‐treated animals had a worsening compared to non‐treated, demonstrated by higher parasitemia and lower survival rate. This result was attributed to the anti‐inflammatory effect of CPE, demonstrated by the higher IL‐10 and IL‐4 values observed in the treated mice compared to the control ones. CPE demonstrated a trypanocidal effect in vitro and a worsening in the in vivo infection due to its anti‐inflammatory activity.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação Araucária

Publisher

Wiley

Subject

Immunology,Parasitology

Reference45 articles.

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