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Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice
Early in the postnatal period, motoneuron axon stimulation can excite motor networks in the spinal cord. Here we tested if these excitatory effects changed across early postnatal development up to postnatal day (P) 24 by when mice are capable of weight-bearing locomotion and locomotor networks are c...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689330/ https://www.ncbi.nlm.nih.gov/pubmed/33294722 http://dx.doi.org/10.1016/j.ibror.2020.10.005 |
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author | Nagaraja, Chetan |
author_facet | Nagaraja, Chetan |
author_sort | Nagaraja, Chetan |
collection | PubMed |
description | Early in the postnatal period, motoneuron axon stimulation can excite motor networks in the spinal cord. Here we tested if these excitatory effects changed across early postnatal development up to postnatal day (P) 24 by when mice are capable of weight-bearing locomotion and locomotor networks are considered functionally mature. This was accomplished in the isolated spinal cord preparation using ventral root evoked entrainment of disinhibited bursts. Ventral root evoked entrainment was defined and characterized over the first 2 weeks of postnatal development, and was found to decline over this period, but entrainment could still be detected in mice as old as P24. Disinhibited bursting could be elicited, and dorsal root evoked entrainment could be recorded as late as P39 and remained unchanged in effectiveness, suggesting that poor tissue viability may not be the cause of the decline in ventral root evoked entrainment. Pharmacological experiments performed on younger animals established that dopamine D2 receptor antagonists and mGluR1 agonists both enhanced ventral root evoked entrainment. In conclusion, the motoneuronal inputs to spinal motor networks via the excitatory pathway is modulated by dopamine and metabotropic glutamate receptors and may be under powerful inhibitory control, which may explain why there is a developmental decline in entrainment. |
format | Online Article Text |
id | pubmed-7689330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-76893302020-12-07 Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice Nagaraja, Chetan IBRO Rep Research Paper Early in the postnatal period, motoneuron axon stimulation can excite motor networks in the spinal cord. Here we tested if these excitatory effects changed across early postnatal development up to postnatal day (P) 24 by when mice are capable of weight-bearing locomotion and locomotor networks are considered functionally mature. This was accomplished in the isolated spinal cord preparation using ventral root evoked entrainment of disinhibited bursts. Ventral root evoked entrainment was defined and characterized over the first 2 weeks of postnatal development, and was found to decline over this period, but entrainment could still be detected in mice as old as P24. Disinhibited bursting could be elicited, and dorsal root evoked entrainment could be recorded as late as P39 and remained unchanged in effectiveness, suggesting that poor tissue viability may not be the cause of the decline in ventral root evoked entrainment. Pharmacological experiments performed on younger animals established that dopamine D2 receptor antagonists and mGluR1 agonists both enhanced ventral root evoked entrainment. In conclusion, the motoneuronal inputs to spinal motor networks via the excitatory pathway is modulated by dopamine and metabotropic glutamate receptors and may be under powerful inhibitory control, which may explain why there is a developmental decline in entrainment. Elsevier 2020-10-27 /pmc/articles/PMC7689330/ /pubmed/33294722 http://dx.doi.org/10.1016/j.ibror.2020.10.005 Text en © 2020 The Author http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Paper Nagaraja, Chetan Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
title | Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
title_full | Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
title_fullStr | Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
title_full_unstemmed | Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
title_short | Ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
title_sort | ventral root evoked entrainment of disinhibited bursts across early postnatal development in mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689330/ https://www.ncbi.nlm.nih.gov/pubmed/33294722 http://dx.doi.org/10.1016/j.ibror.2020.10.005 |
work_keys_str_mv | AT nagarajachetan ventralrootevokedentrainmentofdisinhibitedburstsacrossearlypostnataldevelopmentinmice |