Translating Animal Models of Ischemic Stroke to the Human Condition

被引:9
作者
Matur, Abhijith, V [1 ]
Candelario-Jalil, Eduardo [2 ]
Paul, Surojit [3 ,4 ]
Karamyan, Vardan T. [5 ]
Lee, Jessica D. [6 ]
Pennypacker, Keith [6 ,7 ]
Fraser, Justin F. [1 ,6 ,7 ,8 ,9 ]
机构
[1] Univ Kentucky, Dept Radiol, Lexington, KY 40506 USA
[2] Univ Florida, Dept Neurosci, McKnight Brain Inst, Gainesville, FL 32610 USA
[3] Univ New Mexico, Hlth Sci Ctr, Dept Neurol, Albuquerque, NM USA
[4] Univ New Mexico, Hlth Sci Ctr, Dept Neurosci, Albuquerque, NM USA
[5] Oakland Univ, William Beaumont Sch Med, Dept Fdn Med Studies, Rochester, MI 48063 USA
[6] Univ Kentucky, Dept Neurol, Lexington, KY 40536 USA
[7] Univ Kentucky, Ctr Adv Translat Stroke Sci, Lexington, KY USA
[8] Univ Kentucky, Dept Neurosci, Lexington, KY USA
[9] Univ Kentucky, Dept Neurol Surg, Lexington, KY USA
关键词
Stroke; Cerebrovascular; Animal model; Neuroprotection; Preclinical testing; Therapy; MIDDLE CEREBRAL-ARTERY; MICE LACKING RNF213; THROMBOEMBOLIC STROKE; HEMISPHERIC STROKE; NATURAL-HISTORY; OCCLUSION; RAT; INFARCTION; BRAIN; CRANIECTOMY;
D O I
10.1007/s12975-022-01082-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Ischemic stroke is a leading cause of death and disability. However, very few neuroprotective agents have shown promise for treatment of ischemic stroke in clinical trials, despite showing efficacy in many successful preclinical studies. This may be attributed, at least in part, to the incongruency between experimental animal stroke models used in preclinical studies and the manifestation of ischemic stroke in humans. Most often the human population selected for clinical trials are more diverse than the experimental model used in a preclinical study. For successful translation, it is critical to develop clinical trial designs that match the experimental animal model used in the preclinical study. This review aims to provide a comprehensive summary of commonly used animal models with clear correlates between rodent models used to study ischemic stroke and the clinical stroke pathologies with which they most closely align. By improving the correlation between preclinical studies and clinical trials, new neuroprotective agents and stroke therapies may be more accurately and efficiently identified.
引用
收藏
页码:842 / 853
页数:12
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