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Title

Abnormal GABA-mediated and cerebellar inhibition in women with the fragile X premutation

AuthorsConde, Virginia; Palomar, F. J.; Lama, María José; Martínez, Raquel; Carrillo, Fátima; Pintado, Elisabeth; Mir, Pablo
KeywordsFragile X premutation
Cerebellar inhibition
Transcranial magnetic stimulation
GABAergic system
Intracortical inhibition
Issue Date2013
PublisherAmerican Physiological Society
CitationJournal of Neurophysiology 109: 1315-1322 (2013)
AbstractThe fragile X syndrome is a mutation-driven developmental disorder caused by a repetition over 200 times of the CGG trinucleotide situated in the 5′-untranslated region of the fragile X mental retardation 1 gene (FMR1). The interval between 55 and 199 CGG repeats, which is over the normal range but below full mutation, is named fragile X premutation. Recent studies have focused on the asymptomatic state of fragile X premutation carriers and their potentially relevant preclinical features. However, the underlying neurological mechanisms leading to altered functions in fragile X premutation carriers are still poorly understood. In this study, we wanted to test the hypothesis that asymptomatic women who carry the fragile X premutation present GABAergic and cerebellar abnormalities compared with healthy women without the premutation. We performed noninvasive brain stimulation protocols on both asymptomatic fragile X premutation carriers and controls comprising of measures of GABAA- and GABAB-mediated intracortical inhibition, afferent inhibition, and cerebello-motor functional interactions. Premutation carriers presented an absence of cerebellar inhibition over primary motor cortex as well as a reduced GABAA-mediated intracortical and afferent inhibition compared with healthy nonpremutated controls. These alterations are most probably dependent on a dysfunctional GABAergic mechanism associated with the fragile X premutation condition as previously found in CGG-repeat animal models. Furthermore, the lack of cerebello-motor inhibition could be related to the cerebellar structural abnormalities previously found in carriers of the premutation. © 2013 the American Physiological Society.
Publisher version (URL)http://doi.org/10.1152/jn.00730.2012
URIhttp://hdl.handle.net/10261/142725
DOI10.1152/jn.00730.2012
Identifiersissn: 0022-3077
e-issn: 1522-1598
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