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Abstract #4002

In Vivo 1H MRS Metabolic Profiles in Gad1 Haploinsufficient Mouse Brain

Su Xu1, 2, Elizabeth M. Powell3, Andrew D. Marshall1, 2, Rolicia F. Martin3, Rao P. Gullapalli1, 2

1Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, MD, United States; 2Core for Translational Research in Imaging @ Maryland, Baltimore, MD, United States; 3Department of Anatomy & Neurobiolog, University of Maryland School of Medicine, Baltimore, MD, United States

The B6-Gad1tm1.1Bgc mouse expresses decreased levels of glutamic acid decarboxylase (Gad67), the main enzyme that converts glutamate to GABA and presumably are found in epilepsy, schizophrenia and bipolar disorders. Although effective therapies seek to increase GABA levels in vivo, GABA levels have never been established in vivo, nor has the potential compensatory regulation of excitatory neurotransmitters, such as glutamate in this animal model. In the present study, we demonstrate the feasibility of using in vivo high resolution localized 1H MRS in studies of B6-Gad1tm1.1Bgc mouse brain at 7 Tesla to show regional differences in neurotransmitter levels.

Keywords

abnormal acid acquisition affected agents ahead alleles among anatomic anatomy anesthetized animal appears approved array axial body bounds brain candidates care cells cellular central chamber choline circulation coil committee common compatible concentrations confirming contain converting copy cram customized denoted density detected diagnostic differentially disease disorders dorsal drugs element enzyme epilepsy epileptic evaluated excellent exists experimental explain expression feasibility field findings formation function gamma gating gene general glutamate greater heterogeneity heterogeneous heterozygous human in vivo inhibitory institutional isolated laboratory lack linear local localized locations loss maintained male mammalian many martin matched medicine memory metabolic metabolites mice missing mixture monitoring months mouse necessary nervous neurons neurotransmitter neurotransmitters novel nuclear nucleus package patients post potential press print produce protocols pulse quantification radiology rapid rare receiver regulation reliability resolution respiration role scanning schizophrenia school science sensitivity short siblings spectra statistically successful suggest suppressed surface synapses system temperature therapeutic therapies throughout tool translational transmitter view volume warm water