The conditioned medium of murine and human adipose-derived stem cells exerts neuroprotective effects against experimental stroke model

Brain Res. 2012 Jun 21:1461:87-95. doi: 10.1016/j.brainres.2012.04.033. Epub 2012 Apr 24.

Abstract

This study investigated the possible ameliorative effects of adipose-derived stem cells-conditioned medium (ASC-CM) on experimental ischemic stroke. In vivo ischemic stroke was induced in mice after 2h of middle cerebral artery occlusion (MCAO) followed by 22 h reperfusion. Culture of SH-SY5Y human neuroblastoma cells with 100 μM glutamate for 24h was used as an in vitro neuronal apoptosis model. Intracerebroventricular (i.c.v.) administration of 30- and 100-fold concentrated murine ASC-CM 1h prior to MCAO resulted in a dose-dependent reduction in the infarct volume and the brain swelling. The administration of murine ASC-CM immediately after MCAO was also effective, but administration 2h after MCAO was not. Neuroprotective effects of murine ASC-CM were also confirmed in an in vitro model. Pretreatment with 100-fold concentrated murine ASC-CM at 10% of the total culture volume significantly reduced glutamate-induced excitotoxicity in the SH-SY5Y cells. Similar reduction in the MCAO-induced infarction volume was seen following i.c.v. administration of 100-fold concentrated human ASC-CM or murine ASC-CM. In conclusion, ASC-CM appears to exert ameliorative effects on experimental ischemic stroke i\n both in vivo and in vitro models. These findings suggest the feasibility of ASC-CM administration as a therapy for acute stage stroke.

MeSH terms

  • Adipocytes* / pathology
  • Animals
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cells, Cultured
  • Culture Media, Conditioned* / pharmacology
  • Disease Models, Animal*
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Injections, Intraventricular
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neuroprotective Agents / administration & dosage*
  • Random Allocation
  • Stem Cells* / pathology
  • Stroke / pathology
  • Stroke / prevention & control*

Substances

  • Culture Media, Conditioned
  • Neuroprotective Agents