From: Animal models of post-ischemic forced use rehabilitation: methods, considerations, and limitations
Stroke model | Advantages | Disadvantages | References |
---|---|---|---|
MCAo (indirect ischemia) | +Models transient or permanent ischemia; | -Large and variable infarcts; | |
+No craniectomy required; | -Collateral damage due to non-targeted vasculature; | ||
+Results in cortical and striatal damage | -Feeding problems may occur; | ||
+Widely used and well-characterized | -Some mortality | ||
Endothelin-1 (indirect or direct ischemia) | +Models transient ischemia; | -Requires removal of some skull tissue; | |
+Can produce cortical and striatal damage; | -Less control over duration of occlusion; | ||
+Ability to control precise variables (e.g. concentration, injection volume, stereotaxic coordinates) resulting in localized lesions; | -Mechanism of vessel occlusion not well elucidated | ||
+Can be used to model lacunar infarcts | Â | ||
+Low mortality rate | Â | ||
Photothrombosis (indirect or direct ischemia) | +Models permanent ischemia; low mortality rate; | -Requires skull thinning (direct); | |
+Precise control over lesion size and location (direct); | -Can only produce cortical damage (direct); | ||
+Full craniectomy is avoided | -Collateral damage to non-targeted areas (indirect) | ||
 | -No penumbra | ||
Devascularization (direct ischemia) | +Models permanent ischemia; | -Requires removal of skull tissue; | |
+Relatively good control over lesion size location; | -Mechanical damage can occur to surrounding tissue and vessels; | ||
 | -Can produce surface damage only; | ||
 |  | -No penumbra |  |