Rhamnogalacturonan from Ilex paraguariensis: a potential adjuvant in sepsis treatment

Carbohydr Polym. 2013 Feb 15;92(2):1776-82. doi: 10.1016/j.carbpol.2012.11.013. Epub 2012 Nov 12.

Abstract

The present study evaluated the anti-inflammatory activity of a polysaccharide from maté, using a clinically relevant model of sepsis induced by cecal ligation and puncture (CLP). A polysaccharide from maté (SPI) was obtained from aqueous extraction followed by fractionation, being identified as a rhamnogalacturonan with a main chain of →4)-6-OMe-α-D-GalpA-(1→ groups, interrupted by α-L-Rhap units, substituted by a type I arabinogalactan. SPI was tested against induced-polymicrobial sepsis, at doses of 3, 7 and 10 mg/kg. Via oral administration, SPI prevented the late mortality of infected mice by a rate of 60% at 10 mg/kg, in comparison with untreated mice Dexamethasone, used as positive control, was slightly less effective, with an overall survival rate of 16.7% of mice at the end of the observation period. SPI also affected neutrophil influx, avoiding its accumulation in lungs, and significantly decreased tissue expression of iNOS and COX-2. In this context, maté is a potential nutraceutical, and its polysaccharide a promising adjuvant for sepsis treatment, being consumed as tea-like beverages with no related adverse effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement / drug effects
  • Cyclooxygenase 2 / metabolism
  • Gene Expression Regulation, Enzymologic / drug effects
  • Ilex paraguariensis / chemistry*
  • Ligation / adverse effects
  • Male
  • Methylation
  • Mice
  • Neutrophils / cytology
  • Neutrophils / drug effects
  • Nitric Oxide Synthase Type II / metabolism
  • Pectins / chemistry
  • Pectins / isolation & purification
  • Pectins / pharmacology*
  • Pectins / therapeutic use
  • Punctures / adverse effects
  • Sepsis / drug therapy*
  • Sepsis / enzymology
  • Sepsis / etiology
  • Sepsis / immunology
  • Water / chemistry

Substances

  • Water
  • Pectins
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2