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Mitochondrial complex I inhibition produces selective damage to hippocampal subfield CA1 in organotypic slice cultures
Authors:Guangping?Xu,Miguel?A.?Perez-Pinzon,Thomas?J.?Sick  author-information"  >  author-information__contact u-icon-before"  >  mailto:isick@miami.edu"   title="  isick@miami.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Laboratory of Psychiatry and Exp. Alzheimer’s Research, Department of Psychiatry, Innsbruck Medical University, Anichstr. 35, 6020 Innsbruck, Austria;
Abstract:The effects of mitochondrial respiratory chain inhibitors and the excitotoxinN-methyl-D-aspartate (NMDA) on cell death in hippocampal subfields CA1 and CA3 were examined in hippocampal organotypic slice cultures. Slice cultures, 2–3 week old, were exposed for 1 h to either the Complex 1 inhibitors, rotenone or 1-methyl-4-phenylpyridium (MPP+), the Complex II inhibitor 3-nitropropionic acid (3-NP), or the excitotoxin NMDA. Cell death was examined 24 and 48 h following treatment, by measuring propidium iodide (PI) fluorescence. Treatment with 1 μM rotenone caused greater cell death in hippocampal subfield CA1 than CA3. Exposure of hippocampal slice cultures to 10 μM rotenone, to MPP+ or to NMDA resulted in damage to both CA1 and CA3 subfields. 3-NP produced little damage in either subfield. The data suggest that mitochondrial complex I inhibition can produce selective cell damage in hippocampus and in this regard is similar to that observed following hypoxia/ischemia.
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