Sep, 2015
INFLUX OF EXTRACELLULAR ZN(2+) INTO THE HIPPOCAMPAL CA1 NEURONS IS REQUIRED FOR COGNITIVE PERFORMANCE VIA LONG-TERM POTENTIATION
NEUROSCIENCE
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- Volume
- 304
- Number
- First page
- 209
- Last page
- 216
- Language
- English
- Publishing type
- Research paper (scientific journal)
- DOI
- 10.1016/j.neuroscience.2015.07.042
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
Physiological significance of synaptic Zn2+ signaling was examined in the CA1 of young rats. In vivo CA1 long-term potentiation (LTP) was induced using a recording electrode attached to a microdialysis probe and the recording region was locally perfused with artificial cerebrospinal fluid (ACSF) via the microdialysis probe. In vivo CA1 LTP was inhibited under perfusion with CaEDTA and ZnAF-2DA, extracellular and intracellular Zn2+ chelators, respectively, suggesting that the influx of extracellular Zn2+ is required for in vivo CA1 LTP induction. The increase in intracellular Zn2+ was chelated with intracellular ZnAF-2 in the CA1 1 h after local injection of ZnAF-2DA into the CA1, suggesting that intracellular Zn2+ signaling induced during learning is blocked with intracellular ZnAF-2 when the learning was performed 1 h after ZnAF-2DA injection. Object recognition was affected when training of object recognition test was performed 1 h after ZnAF-2DA injection. These data suggest that intracellular Zn2+ signaling in the CA1 is required for object recognition memory via LTP. Surprisingly, in vivo CA1 LTP was affected under perfusion with 0.1-1 mu M ZnCl2, unlike the previous data that in vitro CA1 LTP was enhanced in the presence of 1-5 mu M ZnCl2. The influx of extracellular Zn2+ into CA1 pyramidal cells has bidirectional action in CA1 LTP. The present study indicates that the degree of extracellular Zn2+ influx into CA1 neurons is critical for LTP and cognitive performance. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
- Link information
- ID information
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- DOI : 10.1016/j.neuroscience.2015.07.042
- ISSN : 0306-4522
- eISSN : 1873-7544
- Pubmed ID : 26204819
- Web of Science ID : WOS:000360008800019