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Animal models for neural diseases.
- Source :
-
Toxicologic pathology [Toxicol Pathol] 2011 Jan; Vol. 39 (1), pp. 167-9. Date of Electronic Publication: 2010 Nov 30. - Publication Year :
- 2011
-
Abstract
- "Animal Models of Neural Disease" was the focus of General Session 5 at a 2010 scientific symposium that was sponsored jointly by the Society of Toxicologic Pathology (STP) and the International Federation of Societies of Toxicologic Pathologists (IFSTP). The objective was to consider issues that dictate the choice of animal models for neuropathology-based studies used to investigate neurological diseases and novel therapeutic agents to treat them. In some cases, no animal model exists that recapitulates the attributes of the human disease (e.g., fibromyalgia syndrome). Alternatively, numerous animal models are available for other conditions, so an essential consideration is selecting the most appropriate experimental system (e.g., Alzheimer's disease). New technologies (e.g., genetically engineered rodent models) promise the opportunity to generate suitable animal models for syndromes that currently lack any in vivo animal model, while in vitro models offer the opportunity to evaluate xenobiotic effects in specific neural cell populations. The complex nature of neurological disease requires regular reassessment of available and potential options to ensure that animal-derived data sets support translational medicine efforts to improve public health.
- Subjects :
- Alzheimer Disease therapy
Animals
Animals, Genetically Modified
Congresses as Topic
Fibromyalgia pathology
Humans
Nervous System Diseases chemically induced
Neurotoxicity Syndromes therapy
Neurotoxins
Societies, Scientific
Disease Models, Animal
Nervous System Diseases pathology
Neurotoxicity Syndromes pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1533-1601
- Volume :
- 39
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Toxicologic pathology
- Publication Type :
- Academic Journal
- Accession number :
- 21119053
- Full Text :
- https://doi.org/10.1177/0192623310389478