Microvascular structure after embolic focal cerebral ischemia in the rat

Brain Res. 2003 May 16;972(1-2):31-7. doi: 10.1016/s0006-8993(03)02433-8.

Abstract

Objectives: We analyze morphological alterations of cerebral neovascularization after stroke using a new 3D imaging software program.

Methods: Male Wistar rats underwent unilateral embolic middle cerebral artery occlusion (MCAo) by a single fibrin rich clot. Subjects were sacrificed from 1 to 28 days post infarct. Vessel perimeters were measured on coronal sections stained with endothelial cell-specific antibody to von Willebrand's factor. Vessel segment lengths, diameters and number of vessels were analyzed on cerebral microvessels perfused with FITC-dextran 14 days after ischemia using LSCM and a 3-D vessel quantification program.

Results: The mean number of microvessels with enlarged perimeters significantly increased in the ipsilateral cortex at day 7 when compared to the contralateral cortex (29.7+/-14.7 vs. 3.7+/-2.5, P<0.05). Subsequently, differences in the number of microvessels with enlarged perimeters decreased on days 14 and 28. Fourteen days post-MCA occlusion, microvessel segment length (15.0 vs. 26.0 microm, P<0.05) and diameter (3.14 vs. 3.75 microm, P<0.05) significantly decreased in the ipsilateral hemisphere when compared to the contralateral hemisphere, respectively. Furthermore, the mean total number of these smaller microvessels increased in the ipsilateral hemisphere (57.33+/-14.5 vs. 32.22+/-11.7, P<0.05).

Conclusions: Focal cerebral ischemia induces morphological changes (early dilated microvessels followed by decreased microvessel segment length and diameter) that are consistent with newly generated microvessels.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Brain Ischemia / pathology*
  • Brain Ischemia / physiopathology
  • Cerebral Cortex / pathology*
  • Disease Models, Animal
  • Functional Laterality
  • Imaging, Three-Dimensional / methods
  • Infarction, Middle Cerebral Artery / pathology*
  • Male
  • Microcirculation / pathology*
  • Neovascularization, Physiologic
  • Rats
  • Rats, Wistar
  • Time Factors