In Vitro Antileishmanial Activity of Sterols from Trametes versicolor (Bres. Rivarden)

Molecules. 2016 Aug 10;21(8):1045. doi: 10.3390/molecules21081045.

Abstract

Two ergostanes, 5α,8α-epidioxy-22E-ergosta-6,22-dien-3β-ol (1) and 5α-ergost-7,22-dien-3β-ol (2), and a lanostane, 3β-hydroxylanostan-8,24-diene-21-oic acid (trametenolic acid) (3), were isolated from an n-hexane extract prepared from the fruiting body of Trametes versicolor (Bres. Rivarden). The activity of the isolated sterols was evaluated against promastigotes and amastigotes of Leishmania amazonensis Lainson and Shaw, 1972. The lanostane, compound (3), showed the best inhibitory response (IC50 promastigotes 2.9 ± 0.1 μM and IC50 amastigotes 1.6 ± 0.1 μM). This effect was 25-fold higher compared with its cytotoxic effect on peritoneal macrophages from BALB/c mice. Therefore, trametenolic acid could be regarded as a promising lead for the synthesis of compounds with antileishmanial activity.

Keywords: Trametes versicolor; antileishmanial activity; trametenolic acid B.

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Fruiting Bodies, Fungal / chemistry
  • Leishmania / drug effects
  • Macrophages, Peritoneal / drug effects
  • Mice
  • Molecular Structure
  • Sterols / chemistry
  • Sterols / isolation & purification
  • Sterols / pharmacology*
  • Trametes / chemistry*
  • Trypanocidal Agents / chemistry
  • Trypanocidal Agents / isolation & purification
  • Trypanocidal Agents / pharmacology*

Substances

  • Sterols
  • Trypanocidal Agents