Rodent models for dystonia research: Characteristics, evaluation, and utility
- 9 March 2005
- journal article
- review article
- Published by Wiley in Movement Disorders
- Vol. 20 (3) , 283-292
- https://doi.org/10.1002/mds.20364
Abstract
A large number of different genetic and acquired disorders of the nervous system may be associated with dystonia. To elucidate its pathogenesis and to facilitate the discovery of potential novel treatments, there has been a growing interest in the development of animal models and particularly rodent models. Multiple animal models for dystonia have now been developed and partially characterized. The results obtained from studies of these models often lead in very different directions, in part because the different models target different aspects of a very heterogeneous disorder. A recent workshop addressed four main issues affecting those who conduct dystonia research with animal models, including the different ways in which dystonic disorders can be modeled in rodents, key features that constitute a useful model, methods used in the evaluation of these models, and recommendations for future research. This review summarizes the main outcomes of this conference. © 2005 Movement Disorder SocietyKeywords
This publication has 78 references indexed in Scilit:
- Parkin-deficient Mice Exhibit Nigrostriatal Deficits but Not Loss of Dopaminergic NeuronsJournal of Biological Chemistry, 2003
- Normal nigrostriatal innervation but dopamine dysfunction in mice carrying hypomorphic tyrosine hydroxylase allelesJournal of Neuroscience Research, 2003
- Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutationDevelopmental Medicine and Child Neurology, 2002
- Role of the vestibular system in the pathophysiology of spasmodic torticollisJournal of Neurology, Neurosurgery & Psychiatry, 2001
- Gait Analysis in the MousePhysiology & Behavior, 1999
- Functional brain networks in DYT1 dystoniaAnnals of Neurology, 1998
- Animal models of Parkinson's disease: An empirical comparison with the phenomenology of the disease in manJournal Of Neural Transmission-Parkinsons Disease and Dementia Section, 1996
- Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptorNature, 1996
- Transgenic and Knock‐out Mice: Models of Neurological DiseaseBrain Pathology, 1994
- Amphetamine-induced behavioral phenotype in a hypoxanthine-guanine phosphoribosyltransferase-deficient mouse model of Lesch-Nyhan syndrome.Behavioral Neuroscience, 1991