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- W2034143722 abstract "Down syndrome (DS) is the most common genetic cause of mental disability. Based on the homology of Hsa21 and the murine chromosomes Mmu16, Mmu17 and Mmu10, several mouse models of DS have been developed. The most commonly used model, the Ts65Dn mouse, has been widely used to investigate the neural mechanisms underlying the mental disabilities seen in DS individuals. A wide array of neuromorphological alterations appears to compromise cognitive performance in trisomic mice. Enhanced inhibition due to alterations in GABA A -mediated transmission and disturbances in the glutamatergic, noradrenergic and cholinergic systems, among others, has also been demonstrated. DS cognitive dysfunction caused by neurodevelopmental alterations is worsened in later life stages by neurodegenerative processes. A number of pharmacological therapies have been shown to partially restore morphological anomalies concomitantly with cognition in these mice. In conclusion, the use of mouse models is enormously effective in the study of the neurobiological substrates of mental disabilities in DS and in the testing of therapies that rescue these alterations. These studies provide the basis for developing clinical trials in DS individuals and sustain the hope that some of these drugs will be useful in rescuing mental disabilities in DS individuals." @default.
- W2034143722 created "2016-06-24" @default.
- W2034143722 creator A5000769621 @default.
- W2034143722 creator A5012504202 @default.
- W2034143722 creator A5028559801 @default.
- W2034143722 date "2012-01-01" @default.
- W2034143722 modified "2023-10-17" @default.
- W2034143722 title "Mouse Models of Down Syndrome as a Tool to Unravel the Causes of Mental Disabilities" @default.
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