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Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies.

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TLDR
This review and commentary will explore why this may be so, focusing on the central role that genetic models of neurobehavioral disorders have come to occupy in current efforts to identify disease mechanisms and therapies, and champion a two‐pronged approach toward identifying novel therapies for neuro behavioral disorders.
Abstract
Neurobehavioral disorders comprised of neurodegenerative, neurodevelopmental, and psychiatric disorders together represent leading causes of morbidity and mortality. Despite significant academic research and industry efforts to elucidate the disease mechanisms operative in these disorders and to develop mechanism-based therapies, our understanding remains incomplete and our access to tractable therapeutic interventions severely limited. The magnitude of these short-comings can be measured by the growing list of disappointing clinical trials based on initially promising compounds identified in genetic animal models. This review and commentary will explore why this may be so, focusing on the central role that genetic models of neurobehavioral disorders have come to occupy in current efforts to identify disease mechanisms and therapies. In particular, we will highlight the unique pitfalls and challenges that have hampered success in these models as compared to genetic models of non-neurological diseases as well as to symptom-based models of the early 20th century that led to the discovery of all major classes of psychoactive pharmaceutical compounds still used today. Using examples from specific genetic rodent models of human neurobehavioral disorders, we will highlight issues of reproducibility, construct validity, and translational relevance in the hopes that these examples will be instructive toward greater success in future endeavors. Lastly, we will champion a two-pronged approach toward identifying novel therapies for neurobehavioral disorders that makes greater use of the historically more successful symptom-based approaches in addition to more mechanism-based approaches.

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Citations
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Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXS

TL;DR: It is reported that Fmr1 knockout (KO) rats exhibit elevated basal protein synthesis and an increase in mGluR-dependent long-term depression in CA1 of the hippocampus that is independent of new protein synthesis, the first evidence for conservation across mammalian species of cellular and physiological hippocampal phenotypes associated with the loss of FMRP.
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Correction to “Fragile X Syndrome”

Anousheh Mortazavi
- 01 Dec 2011 - 
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Reconsidering animal models used to study autism spectrum disorder: Current state and optimizing future

TL;DR: In this paper , the authors discuss the maximal utility and limitations of behavior in animal models with construct validity and provide guidelines on how in vivo models should be used and reported reliably and rigorously.
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The Pathophysiology of Rett Syndrome With a Focus on Breathing Dysfunctions.

TL;DR: Characteristic breath-holds, obstructive sleep apnea, and aerophagia result in intermittent hypoxia, which, combined with mitochondrial dysfunction, causes oxidative stress-an important driver of the clinical presentation of RTT.
References
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The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions

TL;DR: The authors discuss the etymology and strategy behind the use of endophenotypes in neuropsychiatric research and, more generally, in research on other diseases with complex genetics.

Why Most Published Research Findings Are False

TL;DR: In this paper, the authors discuss the implications of these problems for the conduct and interpretation of research and suggest that claimed research findings may often be simply accurate measures of the prevailing bias.
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