A Comparative Study of Variables Influencing Ischemic Injury in the Longa and Koizumi Methods of Intraluminal Filament Middle Cerebral Artery Occlusion in Mice

PLoS One. 2016 Feb 12;11(2):e0148503. doi: 10.1371/journal.pone.0148503. eCollection 2016.

Abstract

The intraluminal filament model of middle cerebral artery occlusion (MCAO) in mice and rats has been plagued by inconsistency, owing in part to the multitude of variables requiring control. In this study we investigated the impact of several major variables on survival rate, lesion volume, neurological scores, cerebral blood flow (CBF) and body weight including filament width, time after reperfusion, occlusion time and the choice of surgical method. Using the Koizumi method, we found ischemic injury can be detected as early as 30 min after reperfusion, to a degree that is not statistically different from 24 h post-perfusion, using 2,3,5-Triphenyltetrazolium chloride (TTC) staining. We also found a distinct increase in total lesion volume with increasing occlusion time, with 30-45 min a critical time for the development of large, reproducible lesions. Furthermore, although we found no significant difference in total lesion volume generated by the Koizumi and Longa methods of MCAO, nor were survival rates appreciably different between the two at 4 h after reperfusion, the Longa method produces significantly greater reperfusion. Finally, we found no statistical evidence to support the exclusion of data from animals experiencing a CBF reduction of <70% in the MCA territory following MCAO, using laser-Doppler flowmetry. Instead we suggest the main usefulness of laser-Doppler flowmetry is for guiding filament placement and the identification of subarachnoid haemorrhages and premature reperfusion. In summary, this study provides detailed evaluation of the Koizumi method of intraluminal filament MCAO in mice and a direct comparison to the Longa method.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight
  • Brain Ischemia / diagnosis*
  • Brain Ischemia / mortality
  • Brain Ischemia / pathology
  • Cerebrovascular Circulation
  • Coloring Agents / chemistry
  • Coronary Occlusion / diagnosis*
  • Coronary Occlusion / mortality
  • Coronary Occlusion / pathology
  • Disease Models, Animal
  • Laser-Doppler Flowmetry
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Cerebral Artery / pathology*
  • Middle Cerebral Artery / surgery
  • Reperfusion Injury / diagnosis*
  • Reperfusion Injury / mortality
  • Reperfusion Injury / pathology
  • Subarachnoid Hemorrhage / diagnosis*
  • Subarachnoid Hemorrhage / mortality
  • Subarachnoid Hemorrhage / pathology
  • Survival Analysis
  • Tetrazolium Salts / chemistry

Substances

  • Coloring Agents
  • Tetrazolium Salts
  • triphenyltetrazolium

Grants and funding

This work was supported by National Health and Medical Research Council (NHMRC) of Australia via research project grant #1083569, Stanley and John Roth, The Boyarsy family, David King, Doug Battersby, Iain S. Gray in memory of Kylie, Joshua Burger in honor of Marko Burger, Tony and Vivian Howland-Rose, Edith Sheldon in memory of Walter Sheldon, Bill Gruy and SpinalCure Australia. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. No research costs or authors’ salaries were funded by a tobacco company.