Journal article
The influence of the HPG axis on stress response and depressive-like behaviour in a transgenic mouse model of Huntington's disease
X Du, TY Pang, C Mo, T Renoir, DJ Wright, AJ Hannan
Experimental Neurology | Published : 2015
Abstract
Huntington's disease (HD) is an autosomal dominant, neurodegenerative disease caused by a CAG tandem repeat mutation encoding a polyglutamine tract expansion in the huntingtin protein. Depression is among the most common affective symptoms in HD but the pathophysiology is unclear. We have previously discovered sexually dimorphic depressive-like behaviours in the R6/1 transgenic mouse model of HD at a pre-motor symptomatic age. Interestingly, only female R6/1 mice display this phenotype. Sexual dimorphism has not been explored in the human HD population despite the well-established knowledge that the clinical depression rate in females is almost twice that of males. Female susceptibility sugg..
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Awarded by Australian Research Council
Funding Acknowledgements
This work was supported by Project Grant funding (AJH) from the NHMRC (509031) and an ARC Future Fellowship (AJH) (FT100100835). XD is supported by a Melbourne Research Scholarship (University of Melbourne). CM is supported by an Australian Postgraduate Award. TR is supported by a ARC DECRA fellowship (DE140100588). This work was supported by the Victorian Government through the Operational Infrastructure Scheme.