<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Postupna NO</submitter><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>1161-72</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4184945</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>94(10)</volume><pubmed_abstract>Synaptic dysfunction is thought to have an important role in the pathophysiology of neurodegenerative diseases, such as Alzheimer's disease (AD) and Lewy body disease (LBD). To improve our understanding of synaptic alterations in health and disease, we investigated synaptosomes prepared from post-mortem human cerebral cortex, putamen (PT), and two regions of the caudate nucleus, dorso-lateral (DL) and ventro-medial (VM), regions commonly affected in AD and LBD. We observed that the fraction of synaptosomal particles with reactivity for dopamine transporter (DAT) was significantly reduced in the PT and VM caudate of patients with neuropathological diagnosis of LBD. As expected, these differences also were reflected in direct measurements of dopamine (DA) and its metabolite, 3,4-dihydroxyphe</pubmed_abstract><journal>Laboratory investigation; a journal of technical methods and pathology</journal><pubmed_title>Flow cytometry analysis of synaptosomes from post-mortem human brain reveals changes specific to Lewy body and Alzheimer's disease.</pubmed_title><pmcid>PMC4184945</pmcid><funding_grant_id>U01 AG06781</funding_grant_id><funding_grant_id>P50 AG05136</funding_grant_id><funding_grant_id>P50 AG005136</funding_grant_id><funding_grant_id>P50 NS062684</funding_grant_id><funding_grant_id>U01 AG006781</funding_grant_id><pubmed_authors>Latimer C</pubmed_authors><pubmed_authors>Darvas M</pubmed_authors><pubmed_authors>Van Gelder RD</pubmed_authors><pubmed_authors>Postupna NO</pubmed_authors><pubmed_authors>Sherfield EE</pubmed_authors><pubmed_authors>Ojemann JG</pubmed_authors><pubmed_authors>Keene CD</pubmed_authors><pubmed_authors>Montine TJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Flow cytometry analysis of synaptosomes from post-mortem human brain reveals changes specific to Lewy body and Alzheimer's disease.</name><description>Synaptic dysfunction is thought to have an important role in the pathophysiology of neurodegenerative diseases, such as Alzheimer's disease (AD) and Lewy body disease (LBD). To improve our understanding of synaptic alterations in health and disease, we investigated synaptosomes prepared from post-mortem human cerebral cortex, putamen (PT), and two regions of the caudate nucleus, dorso-lateral (DL) and ventro-medial (VM), regions commonly affected in AD and LBD. We observed that the fraction of synaptosomal particles with reactivity for dopamine transporter (DAT) was significantly reduced in the PT and VM caudate of patients with neuropathological diagnosis of LBD. As expected, these differences also were reflected in direct measurements of dopamine (DA) and its metabolite, 3,4-dihydroxyphe</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2025-06-28T03:05:16.677Z</modification><creation>2025-06-28T03:05:16.677Z</creation></dates><accession>S-EPMC4184945</accession><cross_references><pubmed>25068655</pubmed><doi>10.1038/labinvest.2014.103</doi></cross_references></HashMap>