TY - JOUR
T1 - Distal hypoxic stroke
T2 - A new mouse model of stroke with high throughput, low variability and a quantifiable functional deficit
AU - Doyle, Kristian P.
AU - Fathali, Nancy
AU - Siddiqui, Mohammad R.
AU - Buckwalter, Marion S.
N1 - Funding Information:
This work was supported by an Ellison Medical Foundation/AFAR Postdoctoral Fellowship to KPD and NINDS KO8 NS050304 and American Heart Association 10GRNT4140073 to MSB. We would like to thank Dr. Mary Stenzel-Poore for technical support, Dr. Nikola Lessov for performing the intraluminal filament model of MCAO, and Geoffrey Stanley and Dr. Kereshmeh Taravosh-Lahn for their assistance with pilot experiments.
PY - 2012/5/30
Y1 - 2012/5/30
N2 - C57BL/6J are the most commonly used strain of mouse for stroke experiments but vascular anatomy of the Circle of Willis within this strain is extremely variable and the cortex has extensive collateralization. This causes large variability in stroke models that target the middle cerebral artery proximally and confers resistance to ischemia in those that target it distally. We tested the hypothesis that by combining distal middle cerebral artery occlusion with 1. h of hypoxia, we could generate a large lesion that causes a behavioral deficit with low variability. We found that this new distal hypoxic (DH) model of stroke generates a lesion with a volume of 25% of the ipsilateral hemisphere, extends to the motor cortex and causes a behavioral deficit. It also has a very clear border, exceptionally low variability, and can be performed by a single surgeon on up to 30 animals a day. Moreover, survivability is 100% in young adult animals, the model can be performed on old animals, and therapeutic intervention can reduce infarct volume. Therefore DH stroke is an excellent complement to existing stroke models and could be used for preclinical studies in C57BL/6J mice.
AB - C57BL/6J are the most commonly used strain of mouse for stroke experiments but vascular anatomy of the Circle of Willis within this strain is extremely variable and the cortex has extensive collateralization. This causes large variability in stroke models that target the middle cerebral artery proximally and confers resistance to ischemia in those that target it distally. We tested the hypothesis that by combining distal middle cerebral artery occlusion with 1. h of hypoxia, we could generate a large lesion that causes a behavioral deficit with low variability. We found that this new distal hypoxic (DH) model of stroke generates a lesion with a volume of 25% of the ipsilateral hemisphere, extends to the motor cortex and causes a behavioral deficit. It also has a very clear border, exceptionally low variability, and can be performed by a single surgeon on up to 30 animals a day. Moreover, survivability is 100% in young adult animals, the model can be performed on old animals, and therapeutic intervention can reduce infarct volume. Therefore DH stroke is an excellent complement to existing stroke models and could be used for preclinical studies in C57BL/6J mice.
KW - Cerebral ischemia
KW - Circle of Willis variability
KW - Hypoxia
KW - New mouse stroke model
UR - http://www.scopus.com/inward/record.url?scp=84859630685&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84859630685&partnerID=8YFLogxK
U2 - 10.1016/j.jneumeth.2012.03.003
DO - 10.1016/j.jneumeth.2012.03.003
M3 - Article
C2 - 22465679
AN - SCOPUS:84859630685
SN - 0165-0270
VL - 207
SP - 31
EP - 40
JO - Journal of Neuroscience Methods
JF - Journal of Neuroscience Methods
IS - 1
ER -