Abstract

Experimental stroke in rodents, via middle cerebral artery occlusion (MCAO), can be associated with a negative impact on wellbeing and mortality. In hypertensive rodents, pre-stroke craniotomy increased survival and decreased body weight loss post-MCAO. Here we determined the effect, in normotensive Sprague-Dawley rats following 60 minutes MCAO, with or without pre-surgical craniotomy, on post-stroke outcomes in terms of weight loss, neurological deficit, lesion volume and functional outcomes. There was no effect of pre-stroke craniotomy on indicators of wellbeing including survival rate (P = 0.32), body weight loss (P = 0.42) and neurological deficit (P = 0.75). We also assessed common outcome measures following experimental stroke and found no effect of pre-stroke craniotomy on lesion volume as measured by T2-weighted MRI (P = 0.846), or functional performance up to 28 days post-MCAO (staircase test, P = 0.32; adhesive sticker test, P = 0.49; cylinder test, P = 0.38). Thus, pre-stroke craniotomy did not improve animal welfare in terms of body weight loss and neurological deficit. However, it is important, given that a number of drug delivery studies utilise the craniotomy procedure, to note that there was no effect on lesion volume or functional outcome following experimental stroke.

Highlights

  • Cerebral ischemic stroke is a leading cause of death and adult disability

  • All animals showed a decrease in cerebral blood flow (CBF), relative to pre-ischemic CBF values, following middle cerebral artery occlusion (MCAO)

  • There was no correlation between percentage decrease in CBF (38.95 ± 4.21%, n = 14) and lesion volume when corrected for brain swelling (41.43 ± 6.64 mm3, n = 14; r = -0.037, P = 0.90)

Read more

Summary

Introduction

Cerebral ischemic stroke is a leading cause of death and adult disability. Current available treatments are limited in both their utility and effectiveness. Tissue plasminogen activator (tPA) is the only specific pharmacological approach with proven efficacy for ischemic stroke [1,2]. Due to a narrow therapeutic window (

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call