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The terpenic diamine GIB24 inhibits the growth of Trypanosoma cruzi epimastigotes and intracellular amastigotes, with proteomic analysis of drug-resistant epimastigotes.
Azeredo, Camila Maria; Saraiva, Mauricio Frota; de Oliveira, Maristela Ribeiro; Barbosa, Gisele; de Almeida, Mauro Vieira; de Souza, Marcus Vinicius Nora; Soares, Maurilio José.
Affiliation
  • Azeredo CM; Laboratory of Cell Biology, Carlos Chagas Institute/Fiocruz-PR, Curitiba, PR, Brazil.
  • Saraiva MF; Institute of Physics and Chemistry, Federal University of Itajubá, Itajubá, MG, Brazil. Electronic address: mauriciosaraiva@unifei.edu.br.
  • de Oliveira MR; Institute of Physics and Chemistry, Federal University of Itajubá, Itajubá, MG, Brazil.
  • Barbosa G; Department of Chemistry, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.
  • de Almeida MV; Department of Chemistry, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.
  • de Souza MVN; Oswaldo Cruz Foundation, Institute of Technology in Drugs, FarManguinhos, Rio de Janeiro, RJ, Brazil.
  • Soares MJ; Laboratory of Cell Biology, Carlos Chagas Institute/Fiocruz-PR, Curitiba, PR, Brazil.
Chem Biol Interact ; 330: 109165, 2020 Oct 01.
Article in En | MEDLINE | ID: mdl-32771326
ABSTRACT
The effect of N-geranyl-ethane-1,2-diamine dihydochloride (GIB24), a synthetic diamine, was assayed against different developmental forms of the parasitic protozoan Trypanosoma cruzi (strain Dm28c). The compound was effective against culture epimastigote forms (IC50/24h = 5.64 µM; SI = 16.4) and intracellular amastigotes (IC50/24h = 12.89 µM; SI = 7.18), as detected by the MTT methodology and by cell counting, respectively. Incubation of epimastigotes for 6h with 6 µM GIB24 (IC50/24h value) resulted in significant dissipation of the mitochondrial membrane potential, prior to permeabilization of the plasma membrane. Rounded epimastigotes with cell size reduction were observed by scanning electron microscopy. These morpho-physiological changes induced by GIB24 suggest an incidental death process. Treatment of infected Vero cells did not prevent the intracellular amastigotes from completing the intracellular cycle. However, there was a decrease in the number of released parasites, increasing the ratio amastigotes/trypomastigotes. Proteomic analysis of 15 µM GIB24 resistant epimastigotes indicated that the compound acts mainly on mitochondrial components involved in the Krebs cycle and in maintaining the oxidative homeostasis of the parasites. Our data suggest that GIB24 is active against the main morphological forms of T. cruzi.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Terpenes / Trypanosoma cruzi / Drug Resistance / Proteomics / Intracellular Space / Diamines Limits: Animals Language: En Journal: Chem Biol Interact Year: 2020 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Terpenes / Trypanosoma cruzi / Drug Resistance / Proteomics / Intracellular Space / Diamines Limits: Animals Language: En Journal: Chem Biol Interact Year: 2020 Document type: Article Affiliation country: Brazil