AI Article Synopsis

  • - Thiazolidinediones (TZDs), such as pioglitazone, show potential neuroprotective effects in rat models of stroke through various administration routes.
  • - In a study, rats received different doses of oral pioglitazone prior to a simulated stroke (MCAO), with the two higher doses (0.65 mg/kg and 0.40 mg/kg) significantly reducing brain damage and improving motor functions compared to the lowest dose (0.20 mg/kg), which had no significant effects.
  • - The study included assessments of motor and sensory abilities post-stroke using various tests, revealing enhanced recovery in rats treated with the higher doses of pioglitazone.

Article 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 (0.65 mg/kg equivalent to a 45 mg dose in a 70 kg man, 0.40 mg/kg equivalent to a 30 mg dose or 0.20mg/kg to a 15 mg 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 0.40 mg/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.

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-1-4419-7756-4_22DOI Listing

Publication Analysis

Top Keywords

infarction volume
12
oral pioglitazone
8
reduces infarction
8
mcao rats
8
mg/kg equivalent
8
equivalent dose
8
040 mg/kg
8
020mg/kg dose
8
dose
5
pioglitazone reduces
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!