| Literature DB >> 29154037 |
Upasana Roy1, Lara Stute2, Corinna Höfling3, Maike Hartlage-Rübsamen3, Jörg Matysik4, Steffen Roβner3, A Alia5.
Abstract
Age and sex are risk factors of Alzheimer's disease (AD). Among the neurotransmitter systems, gamma-aminobutyric acid (GABA) has been implicated in AD pathogenesis but the relevance of sex-specific GABAergic dysfunction during AD progression remains unknown. In the present study, we utilized state-of-the-art high-resolution magic angle spinning nuclear magnetic resonance to systematically monitor the brain region-, age-, and sex-specific modulation of GABA levels in wild-type and Tg2576 mice with amyloid pathology. In addition, we followed the possible role of reactive astrocytes in sex-specific GABA modulation. In female Tg2576 mice, hippocampal GABA levels were significantly elevated, along with higher number of reactive astrocytes and amyloid deposition. The elevated GABA was found to be produced via the monoamine oxidase-B route from putrescine in reactive astrocytes, more substantially in female than male mice, thus suggesting a role of astrocytes in memory impairment and sex-related differences in AD. Our results paint a coherent model of memory impairment in AD and signify that dynamic changes in regional GABA may be at the root of marked sex disparities observed in AD.Entities:
Keywords: (1)H high-resolution magic angle spinning NMR; Alzheimer's disease; GABA; Longitudinal study; Sex difference; Tg2576 mouse model
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Year: 2017 PMID: 29154037 DOI: 10.1016/j.neurobiolaging.2017.10.015
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673