<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Tolo J</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pubmed_abstract>α-Synuclein (α-Syn) is intimately linked to the etiology of Parkinson's Disease, as mutations and even subtle increases in gene dosage result in early onset of the disease. However, how this protein causes neuronal dysfunction and neurodegeneration is incompletely understood. We thus examined a comprehensive range of physiological parameters in cultured rat primary neurons overexpressing α-Syn at levels causing a slowly progressive neurodegeneration. In contradiction to earlier reports from non-neuronal assay systems we demonstrate that α-Syn does not interfere with essential ion handling capacities, mitochondrial capability of ATP production or basic electro-physiological properties like resting membrane potential or the general ability to generate action potentials. α-Syn also does not a</pubmed_abstract><journal>Frontiers in molecular neuroscience</journal><pagination>49</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5845890</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pathophysiological Consequences of Neuronal α-Synuclein Overexpression: Impacts on Ion Homeostasis, Stress Signaling, Mitochondrial Integrity, and Electrical Activity.</pubmed_title><pmcid>PMC5845890</pmcid><pubmed_authors>Spehlbrink G</pubmed_authors><pubmed_authors>Munari F</pubmed_authors><pubmed_authors>Taschenberger G</pubmed_authors><pubmed_authors>Becker S</pubmed_authors><pubmed_authors>Tolo J</pubmed_authors><pubmed_authors>Capaldi S</pubmed_authors><pubmed_authors>Bahr M</pubmed_authors><pubmed_authors>Stahlberg MA</pubmed_authors><pubmed_authors>Zweckstetter M</pubmed_authors><pubmed_authors>Dean C</pubmed_authors><pubmed_authors>Kues J</pubmed_authors><pubmed_authors>Kugler S</pubmed_authors><pubmed_authors>Leite K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pathophysiological Consequences of Neuronal α-Synuclein Overexpression: Impacts on Ion Homeostasis, Stress Signaling, Mitochondrial Integrity, and Electrical Activity.</name><description>α-Synuclein (α-Syn) is intimately linked to the etiology of Parkinson's Disease, as mutations and even subtle increases in gene dosage result in early onset of the disease. However, how this protein causes neuronal dysfunction and neurodegeneration is incompletely understood. We thus examined a comprehensive range of physiological parameters in cultured rat primary neurons overexpressing α-Syn at levels causing a slowly progressive neurodegeneration. In contradiction to earlier reports from non-neuronal assay systems we demonstrate that α-Syn does not interfere with essential ion handling capacities, mitochondrial capability of ATP production or basic electro-physiological properties like resting membrane potential or the general ability to generate action potentials. α-Syn also does not a</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-04T09:06:00.315Z</modification><creation>2019-03-26T23:22:48Z</creation></dates><accession>S-EPMC5845890</accession><cross_references><pubmed>29563864</pubmed><doi>10.3389/fnmol.2018.00049</doi></cross_references></HashMap>