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pubmed-article:7545016pubmed:abstractTextSmall subsets of central neurons possessing Ca2+ permeable AMPA/kainate channels can be identified by a histochemical stain based on kainate-stimulated Co2+ uptake (Co2+(+)neurons) and are unusually vulnerable to AMPA/kainate receptor-mediated injury. Using brief kainate exposures (which selectively destroy Co2+(+) neurons) along with kainate triggered 45Ca2+ influx measurements, we estimate kainate to cause an unusually high rate of Ca2+ influx into Co2+(+) neurons. Also, while fura-2 Ca2+ imaging revealed low (10 microM) kainate exposures to preferentially induce intracellular free Ca2+ ([Ca2+]i) elevations in Co2+(+) neurons, intense (100 microM) kainate exposures used in the 45Ca2+ influx studies triggered comparable [Ca2+]i rises in all neurons. These findings suggest that the exceptional vulnerability of Co2+(+) neurons to AMPA/kainate receptor-mediated injury reflects a high rate of agonist triggered Ca2+ influx, and that [Ca2+]i rises may only poorly reflect influx rate.lld:pubmed
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pubmed-article:7545016pubmed:pagination1089-92lld:pubmed
pubmed-article:7545016pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:7545016pubmed:year1995lld:pubmed
pubmed-article:7545016pubmed:articleTitleCa2+ permeable AMPA/kainate channels permit rapid injurious Ca2+ entry.lld:pubmed
pubmed-article:7545016pubmed:affiliationDepartment of Neurology, University of California, Irvine 92717-4290, USA.lld:pubmed
pubmed-article:7545016pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7545016pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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