Tests to assess motor phenotype in mice: a user's guide

被引:490
作者
Brooks, Simon P. [1 ]
Dunnett, Stephen B. [1 ]
机构
[1] Cardiff Univ, Sch Biosci, Brain Repair Grp, Cardiff CF10 3AX, Wales
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
DOPA-INDUCED DYSKINESIA; INBRED MOUSE STRAINS; EMBRYONIC STEM-CELLS; LURCHER MUTANT MICE; HUNTINGTONS-DISEASE; PARKINSONS-DISEASE; TRANSGENIC MICE; PREPULSE INHIBITION; BEHAVIORAL DEFICITS; STARTLE RESPONSE;
D O I
10.1038/nrn2652
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The characterization of mouse models of human disease is essential for understanding the underlying pathophysiology and developing new therapeutics. Many diseases are often associated with more than one model, and so there is a need to determine which model most closely represents the disease state or is most suited to the therapeutic approach under investigation. In the case of neurological disease, motor tests provide a good read-out of neurological function. This overview of available motor tasks aims to aid researchers in making the correct choice of test when attempting to tease out a transgenic phenotype or when assessing the recovery of motor function following therapeutic intervention.
引用
收藏
页码:519 / 529
页数:11
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