COG1410, a novel apolipoprotein-E mimetic, improves functional and morphological recovery in a rat model of focal brain ischemia

J Neurosci Res. 2009 Feb 15;87(3):677-82. doi: 10.1002/jnr.21874.

Abstract

Apolipoprotein E (apoE) is the primary apolipoprotein synthesized in the brain in response to injury with known neuroprotective effects exerted through antioxidant, antiinflammatory, antiexcitotoxic, and neurotrophic mechanisms. We have previously demonstrated that COG1410, an apoE mimetic peptide, exerts neuroprotective and antiinflammatory effects in a murine model of traumatic brain injury (TBI). As in TBI, ischemia-reperfusion injury is a component of acute stroke, which displays a pharmacogenetic association with the APOE4 gene. Using an intraluminal middle cerebral occlusion (MCAO) model in rats, we found that a single intravenous injection of COG1410 at 120 min post-MCAO significantly improved vestibulomotor function, decreased poststroke locomotor asymmetry, and decreased infarct volume of the ipsilateral hemisphere. These results support further exploration of a novel apoE-mimetic peptide, COG1410, as a therapeutic treatment for stroke.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apolipoproteins E / administration & dosage
  • Apolipoproteins E / therapeutic use*
  • Brain / blood supply
  • Brain / drug effects
  • Brain / pathology
  • Brain / physiopathology
  • Disease Models, Animal
  • Infarction, Middle Cerebral Artery / drug therapy*
  • Infarction, Middle Cerebral Artery / physiopathology
  • Ketamine / pharmacology
  • Male
  • Motor Activity / drug effects*
  • Postural Balance / drug effects*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Apolipoproteins E
  • COG1410
  • Ketamine