Title:The Potential of Secondary Metabolites from Plants as Drugs or Leads
against Trypanosoma cruzi-An Update from 2012 to 2021
Volume: 23
Issue: 3
Author(s): Henrique Barbosa, Fernanda Thevenard, Juliana Quero Reimão, Andre Gustavo Tempone, Kathia Maria Honorio and Joao Henrique Ghilardi Lago*
Affiliation:
- Center of Natural Sciences and Humanities, Federal University of ABC, São Paulo, 09210-180, Brazil
Keywords:
Trypanosoma cruzi, Chagas disease, Natural products, Terpenoids, Alkaloids, Phenylpropanoids, Quinones, Polyketides.
Abstract:
Background: Chagas disease (American Trypanosomiasis) is classified by the World
Health Organization (WHO) as one of the seventeen neglected tropical diseases (NTD), affecting,
mainly, several regions of Latin America.
Introduction: However, immigration has expanded the range of this disease to other continents.
Thousands of patients with Chagas disease die annually, yet no new therapeutics for Chagas disease
have been approved, with only nifurtimox and benznidazole available. Treatment with these drugs
presents several challenges, including protozoan resistance, toxicity, and low efficacy. Natural
products, including the secondary metabolites found in plants, offer a myriad of complex structures
that can be sourced directly or optimized for drug discovery.
Methods: Therefore, this review aims to assess the literature from the last 10 years (2012-2021) and
present the anti-T. cruzi compounds isolated from plants in this period, as well as briefly discuss
computational approaches and challenges in natural product drug discovery. Using this approach,
more than 350 different metabolites were divided based on their biosynthetic pathway alkaloids,
terpenoids, flavonoids, polyketides, and phenylpropanoids which displayed activity against different
forms of this parasite epimastigote, trypomastigote and more important, the intracellular form,
amastigote.
Conclusion: In this aspect, there are several compounds with high potential which could be considered
as a scaffold for the development of new drugs for the treatment of Chagas disease-for this,
more advanced studies must be performed including pharmacokinetics (PK) and pharmacodynamics
(PD) analysis as well as conduction of in vivo assays, these being important limitations in the discovery
of new anti-T. cruzi compounds.