Antinociceptive compounds and LC-DAD-ESIMSn profile from Dictyoloma vandellianum leaves

PLoS One. 2019 Oct 29;14(10):e0224575. doi: 10.1371/journal.pone.0224575. eCollection 2019.

Abstract

Limonoids, quinolone alkaloids and chromones have been reported as constituents of Dictyoloma vandellianum Adr. Juss. (Rutaceae). Although those compounds are known for their biological activities, only the anti-inflammatory activity of chromones isolated from the underground parts has been evaluated. There are no studies of the pharmacological properties of the aerial parts of D. vandellianum. The present study was carried out to determine the phytochemical profile and antinociceptive activity of the methanol extract, fractions and isolated compounds of leaves of D. vandellianum. The phytochemical profile was performed by HLPC-DAD-ESIMSn and pure substances obtained were characterized by MS and NMR spectroscopy. The antinociceptive activity was assessed using the formalin assay in mice, and the motor function in the rotarod test. ME and all the fractions obtained from ME produced antinociceptive effects. Among them, the ethyl ether fraction was the most active. Data from HPLC-DAD-ESIMSn showed that the ethyl ether fraction presented 42 compounds. The major compounds isolated from this fraction-gallic acid, methyl gallate and 1,2,6-tri-O-galloyl-β-d-glucopyranose-were tested and produced antinociceptive effects. Gallic acid, methyl gallate and 1,2,6-tri-O-galloyl-β-d-glucopyranose at antinociceptive doses did not affect the motor performance in mice in the rotarod test. This work is the first report of the occurrence of gallotanins in D. vandellianum. In addition, the pharmacological study showed that D. vandellianum leaves present antinociceptive activity, probably induced by gallic acid, methyl gallate and 1,2,6-tri-O-galloyl-β-d-glucopyranose.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemistry
  • Analgesics / chemistry*
  • Animals
  • Chromatography, High Pressure Liquid / methods
  • Chromatography, Liquid / methods
  • Chromones / analysis
  • Gas Chromatography-Mass Spectrometry / methods
  • Limonins / analysis
  • Male
  • Methanol / analysis
  • Mice
  • Phytochemicals / analysis
  • Plant Extracts / pharmacology
  • Plant Leaves / chemistry*
  • Plant Leaves / metabolism
  • Rutaceae / chemistry*
  • Rutaceae / genetics

Substances

  • Alkaloids
  • Analgesics
  • Chromones
  • Limonins
  • Phytochemicals
  • Plant Extracts
  • Methanol

Grants and funding

This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico process number CFV, MSS, JFT: INCT/Rennofito 465536/2014-0. This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) Finance Code 001. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.