This project will focus on two areas of extra-striatal pathology in HD (cortex and amygdala) and their relationship to possible pathogenetic mechanisms and to non-motor clinical features (dementia, depression, apathy and irritability). Our preliminary cell counting data suggests that neuronal loss occurs in layers III and V and especially in layer VI. We propose to quantify neuronal depletion using computer-assisted neuronal cell counting methods. The regional topography of changes in relation to the corticostriatal and striato-pallido-thalamo-cortical connections may allow inferences about the pathogenesis of cortical neuropathology. In addition, we will correlate the extent of pathology in four cortical regions with nonmotor clinical symptoms. We will better define the neurotransmitter specificity of the cortical pathology using in situ hybridization, receptor autoradiography, and immunocytochemistry.
Our second aim i s to investigate pathology in the amygdala and associated nuclei, regions where pathologic changes may result in psychiatric abnormalities. Neurotransmitter-specific studies, including our preliminary data on opiate receptors, have suggested that these regions are affected. We will count neurons, using methods similar to the cortical studies; study the details of neurotransmitter-related lesions using in situ hybridization, immunocytochemistry, and receptor autoradiography; and correlate the results with clinical symptoms. Taken together, these studies should further our knowledge of the pathogenetic mechanisms of HD and the relationship between neuropathology and clinical symptoms.

Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Faria, Andreia V; Ratnanather, J Tilak; Tward, Daniel J et al. (2016) Linking white matter and deep gray matter alterations in premanifest Huntington disease. Neuroimage Clin 11:450-460
Krause, Amanda; Mitchell, Claire; Essop, Fahmida et al. (2015) Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype. Am J Med Genet B Neuropsychiatr Genet 168:573-85
Ross, Christopher A; Pantelyat, Alex; Kogan, Jane et al. (2014) Determinants of functional disability in Huntington's disease: role of cognitive and motor dysfunction. Mov Disord 29:1351-8
Hua, Jun; Unschuld, Paul G; Margolis, Russell L et al. (2014) Elevated arteriolar cerebral blood volume in prodromal Huntington's disease. Mov Disord 29:396-401
Unschuld, Paul G; Liu, Xinyang; Shanahan, Megan et al. (2013) Prefrontal executive function associated coupling relates to Huntington's disease stage. Cortex 49:2661-73
Nucifora, Leslie G; Burke, Kathleen A; Feng, Xia et al. (2012) Identification of novel potentially toxic oligomers formed in vitro from mammalian-derived expanded huntingtin exon-1 protein. J Biol Chem 287:16017-28
Jiang, Mali; Wang, Jiawei; Fu, Jinrong et al. (2012) Neuroprotective role of Sirt1 in mammalian models of Huntington's disease through activation of multiple Sirt1 targets. Nat Med 18:153-8
Biglan, K M; Dorsey, E R; Evans, R V V et al. (2012) Plasma 8-hydroxy-2'-deoxyguanosine Levels in Huntington Disease and Healthy Controls Treated with Coenzyme Q10. J Huntingtons Dis 1:65-9
Unschuld, Paul G; Joel, Suresh E; Liu, Xinyang et al. (2012) Impaired cortico-striatal functional connectivity in prodromal Huntington's Disease. Neurosci Lett 514:204-9
Unschuld, Paul G; Joel, Suresh E; Pekar, James J et al. (2012) Depressive symptoms in prodromal Huntington's Disease correlate with Stroop-interference related functional connectivity in the ventromedial prefrontal cortex. Psychiatry Res 203:166-74

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