Vibrissa-signaled eyeblink conditioning induces somatosensory cortical plasticity
Open accessAbstract
Whisker deflection conditioned stimuli (CS) were demonstrated to activate physiologically and anatomically defined barrels in the contralateral somatosensory cortex and to support trace-eyeblink conditioned responses when paired with corneal airpuff unconditioned stimuli in rabbits. Analysis of cytochrome-oxidase-stained somatosensory whisker-associated cortical barrels revealed a row-specific expansion of the conditioned compared with the nontrained hemisphere. This expansion was not evident in pseudo-conditioned rabbits, suggesting that this expansion of conditioned cortical barrels in response to a hippocampal- and forebrain-dependent learning task (trace conditioning) is associative rather than activity dependent. Using whisker stimulation as a CS in the well studied eyeblink conditioning paradigm will facilitate characterizing sensory cortical involvement in controlling and modulating an associatively learned response at the neural systems and cellular level.
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Epileptiform activity during initiation of epileptic discharges in the neocortex suggests enhanced postsynaptic activity.
“Epileptiform activity during initiation of epileptic discharges in the neocortex [52] suggests enhanced postsynaptic activity [53].”
From Hippocampal neuro-networks and dendritic spine perturbations in epileptogenesis are attenuated by neuroprotectin D1 (2015) · cites this paper as [53]
The aberrant neuronal network activity observed from LFP recordings may reflect linearly-summed postsynaptic potentials from small populations of principal cells that take place in dendritic spines that survive after status epilepticus.
“The aberrant neuronal network activity observed here from LFP recordings may reflect the linearly-summed postsynaptic potentials from small populations of principal cells [21, 53] that takes place in dendritic spines [34, 54] that survive after SE.”
From Hippocampal neuro-networks and dendritic spine perturbations in epileptogenesis are attenuated by neuroprotectin D1 (2015) · cites this paper as [53]
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References 77 · Cited by 66
- Authors
- Galvez, R., Weiss, C., Weible, A. P., & Disterhoft, J. F.
- Affiliations
- Northwestern University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2006-05-31
- Volume
- 26
- Issue
- 22
- Pages
- 6062-6068
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6675235
- OpenAlex
- W2005407591
- Cited by
- 66
- References
- 77
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 3 · 2019: 4 · 2018: 2 · 2017: 5 · 2016: 6 · 2015: 5 · 2014: 6 · 2013: 4 · 2012: 8
- FWCI
- 1.78
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (T32 AG-20506, T32AG020506)
- National Institute of Mental Health (R01-MH-47340, R01MH047340)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- eyeblink conditioning, trace conditioning, somatosensory cortex, cortical plasticity, barrel cortex, whisker stimulation, conditioned stimulus, associative learning, cytochrome c oxidase, hippocampus-dependent learning, rabbits
- MeSH terms
- Animals, Blinking, Cerebral Cortex, Conditioning, Psychological, Electron Transport Complex IV, Electrophysiology, Female, Functional Laterality, Neuronal Plasticity, Physical Stimulation, Rabbits, Somatosensory Cortex, Stereotaxic Techniques, Vibrissae, Models, Animal
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