In Vitro Investigation of Synaptic Plasticity
- 1Centre for Research in Neuroscience, Department of Neurology and Neurosurgery, The Research Institute of the McGill University Health Centre, Montréal General Hospital, Montréal, Québec H3G 1A4, Canada
- 2Integrated Program in Neuroscience, McGill University, Montréal, Quebec H3A 2B4, Canada
- 3Department of Biology, Bellini Life Sciences Building, McGill University, Montréal, Québec H3G 0B1, Canada
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↵4 These authors contributed equally to this work.
Abstract
A classical in vitro model for investigation of information storage in the brain is based on the acute hippocampal slice. Here, repeated high-frequency stimulation of excitatory Schaeffer collaterals making synapses onto pyramidal cells in the hippocampal CA1 region leads to strengthening of evoked field-recording responses—long-term potentiation (LTP)—in keeping with Hebb’s postulate. This model remains tremendously influential for its reliability, specificity, and relative ease of use. More recent plasticity studies have explored various other brain regions including the neocortex, which often requires more laborious whole-cell recordings of synaptically connected pairs of neurons, to ensure that the identities of recorded cells are known. In addition, with this experimental approach, the spiking activity can be controlled with millisecond precision, which is necessary for the study of spike-timing-dependent plasticity (STDP). Here, we provide protocols for in vitro study of hippocampal CA1 LTP using field recordings, and of STDP in synaptically connected pairs of layer-5 pyramidal cells in acute slices of rodent neocortex.
Footnotes
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↵5 Correspondence: jesper.sjostrom{at}mcgill.ca
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From the Ion Channels collection, edited by Paul J. Kammermeier, Ian Duguid, and Stephan Brenowitz.
- © 2016 Cold Spring Harbor Laboratory Press
