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Abstract #4130

HYPOTHALAMIC-PITUITARY-GONADAL AXIS DYSREGULATION ALTERS RESTING STATE FUNCTIONAL CONNECTIVITY IN A MOUSE MODEL OF ALZHEIMER’S DISEASE

FIRAT KARA1, Michael Belloy1, Garima Yadav1, An Langbeen2, Jules Jacobs3, Disha Shah1, Steffen Roßner4, Peter Ponsaerts5, Marleen Verhoye1, and Annemie Van Der Linden1

1Bioimaging Lab, Antwerp University, Antwerp, Belgium, 2Laboratory of Veterinary Physiology and Biochemistry, Antwerp University, Antwerp, Belgium, 3Mathematics, Leiden University, Netherlands, 4Paul Flechsig Institute for Brain Research, University of Leipzig, Leipzig, Germany, 5Experimental Cell Transplantation Group, Antwerp University, Antwerp, Belgium

Dysregulation of hypothalamic pituitary gonadal (HPG) axis signaling with menopause is considered as a risk factor for Alzheimer’s disease (AD). Menopause leads to decreased sex steroid signaling and increased luteinizing hormone signaling which may have profound effects on many cellular processes that predispose to neurodegeneration and impairment in cognitive function. The effects of amyloid production on resting state BOLD fMRI using functional connectivity analysis in a mouse model of AD have been previously published. However how HPG axis dysregulation affect resting state functional connectivity in a mouse model of AD has not been studied. Here we show that ovariectomized AD mice, a commonly used animal model to study menopause related hormonal changes in the HPG axis, exhibit alterations in resting state connectivity in the mouse default mode network connectivity. These findings establish a causal link between AD and HPG axis dysregulation.

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