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Oral Pioglitazone Reduces Infarction Volume and Improves Neurologic Function Following MCAO in Rats

  • D’Arbra Blankenship
  • Jon Niemi
  • Elizabeth Hilow
  • Molly Karl
  • Sophia SundararajanEmail author
Conference paper
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 701)

Abstract

Thiazolidinediones (TZDs) are neuroprotective in rodent stroke models using intra-peritoneal, intra-venous and inter-ventricular routes of administration.We tested if oral pioglitazone at doses similar to those used by humans to treat diabetes reduces infarction volume following middle cerebral artery occlusion (MCAO) in the rat. Rats were fed DMSO or pioglitazone (0.65mg/kg equivalent to a 45mg dose in a 70kg man, 0.40mg/kg equivalent to a 30mg dose or 0.20mg/kg to a15mg dose) dissolved in DMSO daily for five days prior to 2 hour MCAO. Animals underwent serial functional analysis using the modified neurologic stroke scale (mNSS), the adhesive sticker test and the inclined plane, all of which test motor sensory function. Twenty one days later, MCAO rats were sacrificed and infarct volumes determined. We found significant reductions in the infarct volume using the 0.65 and 0.40mg/kg dose. Furthermore, these rats had improved performance on behavioural assays. The 0.20mg/kg dose did not significantly reduce infarction volume or improve behaviour.

Keywords

Middle Cerebral Artery Occlusion Incline Plane Transient Cerebral Ischemia Reduce Infarction Volume Transient Focal Ischemia 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  • D’Arbra Blankenship
    • 1
  • Jon Niemi
    • 1
  • Elizabeth Hilow
    • 1
  • Molly Karl
    • 1
  • Sophia Sundararajan
    • 1
    • 2
    Email author
  1. 1.Department of NeurologyUniversity Hospitals of Cleveland and Case Western Reserve UniversityClevelandUSA
  2. 2.Department of NeurosciencesUniversity Hospitals of Cleveland and Case Western Reserve UniversityClevelandUSA

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