Cargando…

Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning

Here, we investigate stimulus generalization in a cerebellar learning paradigm, called eyeblink conditioning. Mice were conditioned to close their eyes in response to a 10-kHz tone by repeatedly pairing this tone with an air puff to the eye 250 ms after tone onset. After 10 consecutive days of train...

Descripción completa

Detalles Bibliográficos
Autores principales: Fiocchi, F. R., Dijkhuizen, S., Koekkoek, S. K. E., De Zeeuw, C. I., Boele, H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941640/
https://www.ncbi.nlm.nih.gov/pubmed/35228312
http://dx.doi.org/10.1523/ENEURO.0400-21.2022
_version_ 1784673148123217920
author Fiocchi, F. R.
Dijkhuizen, S.
Koekkoek, S. K. E.
De Zeeuw, C. I.
Boele, H. J.
author_facet Fiocchi, F. R.
Dijkhuizen, S.
Koekkoek, S. K. E.
De Zeeuw, C. I.
Boele, H. J.
author_sort Fiocchi, F. R.
collection PubMed
description Here, we investigate stimulus generalization in a cerebellar learning paradigm, called eyeblink conditioning. Mice were conditioned to close their eyes in response to a 10-kHz tone by repeatedly pairing this tone with an air puff to the eye 250 ms after tone onset. After 10 consecutive days of training, when mice showed reliable conditioned eyelid responses to the 10-kHz tone, we started to expose them to tones with other frequencies, ranging from 2 to 20 kHz. We found that mice had a strong generalization gradient, whereby the probability and amplitude of conditioned eyelid responses gradually decreases depending on the dissimilarity with the 10-kHz tone. Tones with frequencies closest to 10 kHz evoked the most and largest conditioned eyelid responses and each step away from the 10-kHz tone resulted in fewer and smaller conditioned responses (CRs). In addition, we found that tones with lower frequencies resulted in CRs that peaked earlier after tone onset compared with those to tones with higher frequencies. Together, our data show prominent generalization patterns in cerebellar learning. Since the known function of cerebellum is rapidly expanding from pure motor control to domains that include cognition, reward-learning, fear-learning, social function, and even addiction, our data imply generalization controlled by cerebellum in all these domains.
format Online
Article
Text
id pubmed-8941640
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-89416402022-03-29 Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning Fiocchi, F. R. Dijkhuizen, S. Koekkoek, S. K. E. De Zeeuw, C. I. Boele, H. J. eNeuro Research Article: New Research Here, we investigate stimulus generalization in a cerebellar learning paradigm, called eyeblink conditioning. Mice were conditioned to close their eyes in response to a 10-kHz tone by repeatedly pairing this tone with an air puff to the eye 250 ms after tone onset. After 10 consecutive days of training, when mice showed reliable conditioned eyelid responses to the 10-kHz tone, we started to expose them to tones with other frequencies, ranging from 2 to 20 kHz. We found that mice had a strong generalization gradient, whereby the probability and amplitude of conditioned eyelid responses gradually decreases depending on the dissimilarity with the 10-kHz tone. Tones with frequencies closest to 10 kHz evoked the most and largest conditioned eyelid responses and each step away from the 10-kHz tone resulted in fewer and smaller conditioned responses (CRs). In addition, we found that tones with lower frequencies resulted in CRs that peaked earlier after tone onset compared with those to tones with higher frequencies. Together, our data show prominent generalization patterns in cerebellar learning. Since the known function of cerebellum is rapidly expanding from pure motor control to domains that include cognition, reward-learning, fear-learning, social function, and even addiction, our data imply generalization controlled by cerebellum in all these domains. Society for Neuroscience 2022-03-21 /pmc/articles/PMC8941640/ /pubmed/35228312 http://dx.doi.org/10.1523/ENEURO.0400-21.2022 Text en Copyright © 2022 Fiocchi et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Fiocchi, F. R.
Dijkhuizen, S.
Koekkoek, S. K. E.
De Zeeuw, C. I.
Boele, H. J.
Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning
title Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning
title_full Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning
title_fullStr Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning
title_full_unstemmed Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning
title_short Stimulus Generalization in Mice during Pavlovian Eyeblink Conditioning
title_sort stimulus generalization in mice during pavlovian eyeblink conditioning
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941640/
https://www.ncbi.nlm.nih.gov/pubmed/35228312
http://dx.doi.org/10.1523/ENEURO.0400-21.2022
work_keys_str_mv AT fiocchifr stimulusgeneralizationinmiceduringpavlovianeyeblinkconditioning
AT dijkhuizens stimulusgeneralizationinmiceduringpavlovianeyeblinkconditioning
AT koekkoekske stimulusgeneralizationinmiceduringpavlovianeyeblinkconditioning
AT dezeeuwci stimulusgeneralizationinmiceduringpavlovianeyeblinkconditioning
AT boelehj stimulusgeneralizationinmiceduringpavlovianeyeblinkconditioning