4.4 Article

A reproducible Endothelin-1 model of forelimb motor cortex stroke in the mouse

Journal

JOURNAL OF NEUROSCIENCE METHODS
Volume 233, Issue -, Pages 34-44

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jneumeth.2014.05.014

Keywords

Forelimb motor cortex; Injury volume; Behavioral test; Cylinder test; Staircase test; Neural precursor cells; Subventricular zone

Funding

  1. Canadian Institutes of Health Research
  2. Research and Development Corporation of Newfoundland
  3. Heart & Stroke Foundation of Canada Partnership for Stroke Recovery Catalyst grant
  4. Heart & Stroke Foundation of Canada - Keith Griffiths Studentship Award
  5. Heart & Stroke Foundation of Canada Canadian Partnership for Stroke Recovery Graduate Studentship

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Background: Despite the availability of numerous transgenic mouse lines to study the role of individual genes in promoting neural repair following stroke, few studies have availed of this technology, primarily due to the lack of a reproducible ischemic injury model in the mouse. Intracortical injections of Endothelin-1 (ET1) a potent vasoconstrictive agent, reliably produces focal infarcts with concomitant behavioral deficits in rats. In contrast, ET1 infarcts in mice are significantly smaller and do not generate consistent behavioral deficits. New method: We have modified the ET1 ischemia model to target the anterior forelimb motor cortex (aFMC) and show that this generates a reproducible focal ischemic injury in mice with consistent behavioral deficits. Furthermore, we have developed a novel analysis of the cylinder test by quantifying paw-dragging behavior. Results: ET1 injections which damage deep layer neurons in the aFMC generate reproducible deficits on the staircase test. Cylinder test analysis showed no forelimb asymmetry post-injection; however, we observed a novel paw-dragging behavior in mice which is a positive sign of damage to the FMC. Comparison with existing methods: Previous ET1 studies have demonstrated inconsistent behavioral deficits; however, targeting ET1 injections to the aFMC reliably results in staircase deficits. We show that analysis of paw-dragging behavior in the cylinder test is a more sensitive measure of damage to the FMC than the classical forelimb asymmetry analysis. Conclusions: We have developed a focal ischemic injury model in the mouse that results in reproducible behavioral deficits and can be used to test future regenerative therapies. (C) 2014 Elsevier B.V. All rights reserved.

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