Treatment with green tea extract attenuates secondary inflammatory response in an experimental model of spinal cord trauma

Naunyn Schmiedebergs Arch Pharmacol. 2009 Aug;380(2):179-92. doi: 10.1007/s00210-009-0414-z. Epub 2009 Apr 1.

Abstract

In this study, we evaluated the effect of green tea extract (that was administered 25 mg/kg intraperitoneal at 1 and 6 h after injury) in experimental animal model of spinal cord injury. The spinal cord trauma was induced by the application of vascular clips to the dura via a four-level T5-T8 laminectomy. Spinal cord injury in mice resulted in severe trauma characterised by oedema, neutrophilic infiltration and apoptosis. Also, immunohistochemical examination demonstrated a marked increase in immune reactivity for nitrotyrosine. All parameters of inflammation were attenuated by green tea extract. The degree of spinal cord inflammation, nitrotyrosine, poli (ADP-ribosio) synthetase (PARS) and neutrophilic infiltration was markedly reduced. Green tea extract significantly ameliorated the recovery of limb function. Values shown are mean +/- SE mean of ten mice for each group. *p < 0.01 versus sham, degrees p < 0.01 versus spinal cord injury. Taken together, our results clearly demonstrate that green tea extract treatment ameliorates spinal cord injury oxidative stress.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Disease Models, Animal
  • Edema / drug therapy
  • Edema / etiology
  • Immunohistochemistry
  • Inflammation / drug therapy*
  • Inflammation / etiology
  • Male
  • Mice
  • Neutrophil Infiltration / drug effects
  • Oxidative Stress / drug effects
  • Plant Extracts / pharmacology*
  • Poly(ADP-ribose) Polymerases / drug effects
  • Poly(ADP-ribose) Polymerases / metabolism
  • Spinal Cord Injuries / drug therapy*
  • Spinal Cord Injuries / physiopathology
  • Tea / chemistry*
  • Time Factors
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism

Substances

  • Plant Extracts
  • Tea
  • 3-nitrotyrosine
  • Tyrosine
  • Poly(ADP-ribose) Polymerases