| Full text | |
| Author(s): |
Alves Conserva, Geanne A.
[1]
;
da Costa-Silva, Thais A.
[1]
;
Amaral, Maiara
[2]
;
Antar, Guilherme M.
[3]
;
Neves, Bruno J.
[4, 5]
;
Andrade, Carolina H.
[4]
;
Tempone, Andre G.
[2]
;
Lago, Joao Henrique G.
[1]
Total Authors: 8
|
| Affiliation: | [1] Univ Fed ABC, Ctr Ciencias Nat & Humans, BR-09210180 Sao Paulo - Brazil
[2] Adolfo Lutz Inst, Ctr Parasitol & Micol, BR-01246902 Sao Paulo - Brazil
[3] Univ Sao Paulo, Inst Biociencias, Dept Bot, BR-05508090 Sao Paulo - Brazil
[4] Univ Fed Goias, Fac Farm, Lab Modelagem Mol & Drug Design, LabMol, BR-75070290 Goiania, Go - Brazil
[5] Ctr Univ Ancipolis UniE, Lab Quimioinformat, BR-75070290 Goiania, Go - Brazil
Total Affiliations: 5
|
| Document type: | Journal article |
| Source: | Phytomedicine; v. 54, p. 302-307, FEB 15 2019. |
| Web of Science Citations: | 1 |
| Abstract | |
Background: From a previous screening of Brazilian biodiversity for antitrypanosomal activity, the n-hexane extract from twigs of Nectandra oppositifolia (Lauraceae) demonstrated in vitro activity against Trypanosoma cruzi. Purpose: To perform the isolation and chemical characterization of bioactive compounds from n-hexane extract from twigs of N. oppositifolia and evaluate their therapeutical potential as well as to elucidate their mechanism of action against T. cruzi. Methods/Study design: Bioactivity-guided fractionation of the n-hexane extract from twigs of N. oppositifolia af-forded three related butenolides: isolinderanolide D (1), isolinderanolide E (2) and secosubamolide A (3). These compounds were evaluated in vitro against T. cruzi (trypomastigote and amastigote forms) and against NCTC (L929) cells for mammalian cytotoxicity. Additionally, phenotypic analyzes of compounds-treated parasites were performed: alterations in the plasma membrane permeability, plasma membrane electric potential (Delta Psi(p)), mitochondrial membrane potential (Delta Psi(m)) and induction of ROS. Results: Compounds 1-3 were effective against T. cruzi, with IC50 values of 12.9, 29.9 and 12.5 mu M for trypomastigotes and 25.3, 10.1 and 12.3 mu M for intracellular amastigotes. Furthermore, it was observed alteration in the mitochondrial membrane potential (Delta Psi(m)) of parasites treated with butenolides 1-3. These compounds caused no alteration to the parasite plasma membrane, and the deregulation of the mitochondria might be an early event to cell death. In addition, in silico studies showed that all butenolides were predicted to be non-mutagenic, non-carcinogenic, non hERG blockers, with acceptable human intestinal absorption, low inhibitory promiscuity with the main five CYP isoforms, and with high metabolic stability. Otherwise, tested butenolides showed unfavorable blood-brain barrier penetration (BBB +). Conclusion: Our results demonstrated the anti-T. cruzi effects of compounds 1-3 isolated from N. oppositifolia and indicated that the lethal effect of these compounds in trypomastigotes of T. cruzi could be associated to the alteration in the mitochondrial membrane potential (Delta Psi(m)). (AU) | |
| FAPESP's process: | 16/20633-6 - Bioactive metabolites from Nectandra oppositifolia Nees & Mart. (Lauraceae): molecular characterization, in vitro and in vivo antiparasitic potential evaluation and determination of mechanism of action |
| Grantee: | Geanne Alexsandra Alves Conserva |
| Support Opportunities: | Scholarships in Brazil - Doctorate |
| FAPESP's process: | 15/23403-9 - Rational Pre-Clinical Study of New Drug Candidates Against Neglected Protozoan Diseases Using Pharmacokinetic Approaches |
| Grantee: | André Gustavo Tempone Cardoso |
| Support Opportunities: | Regular Research Grants |
| FAPESP's process: | 18/07885-1 - Biomolecules from plant species of remnant areas of the Atlantic Forest and Cerrado to treat neglected tropical diseases - chemical and pharmacological aspects |
| Grantee: | João Henrique Ghilardi Lago |
| Support Opportunities: | BIOTA-FAPESP Program - Regular Research Grants |