Cargando…

Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity

Brain-derived neurotrophic factor (BDNF) is critically involved in the pathophysiology of chronic pain. However, the mechanisms of BDNF action on specific neuronal populations in the spinal superficial dorsal horn (SDH) requires further study. We used chronic BDNF treatment (200 ng/ml, 5–6 days) of...

Descripción completa

Detalles Bibliográficos
Autores principales: Alles, Sascha R. A., Odem, Max A., Lu, Van B., Cassidy, Ryan M., Smith, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838274/
https://www.ncbi.nlm.nih.gov/pubmed/33500423
http://dx.doi.org/10.1038/s41598-021-81269-6
_version_ 1783643137794637824
author Alles, Sascha R. A.
Odem, Max A.
Lu, Van B.
Cassidy, Ryan M.
Smith, Peter A.
author_facet Alles, Sascha R. A.
Odem, Max A.
Lu, Van B.
Cassidy, Ryan M.
Smith, Peter A.
author_sort Alles, Sascha R. A.
collection PubMed
description Brain-derived neurotrophic factor (BDNF) is critically involved in the pathophysiology of chronic pain. However, the mechanisms of BDNF action on specific neuronal populations in the spinal superficial dorsal horn (SDH) requires further study. We used chronic BDNF treatment (200 ng/ml, 5–6 days) of defined-medium, serum-free spinal organotypic cultures to study intracellular calcium ([Ca(2+)](i)) fluctuations. A detailed quantitative analysis of these fluctuations using the Frequency-independent biological signal identification (FIBSI) program revealed that BDNF simultaneously depressed activity in some SDH neurons while it unmasked a particular subpopulation of ‘silent’ neurons causing them to become spontaneously active. Blockade of gap junctions disinhibited a subpopulation of SDH neurons and reduced BDNF-induced synchrony in BDNF-treated cultures. BDNF reduced neuronal excitability assessed by measuring spontaneous excitatory postsynaptic currents. This was similar to the depressive effect of BDNF on the [Ca(2+)](i) fluctuations. This study reveals novel regulatory mechanisms of SDH neuronal excitability in response to BDNF.
format Online
Article
Text
id pubmed-7838274
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-78382742021-01-27 Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity Alles, Sascha R. A. Odem, Max A. Lu, Van B. Cassidy, Ryan M. Smith, Peter A. Sci Rep Article Brain-derived neurotrophic factor (BDNF) is critically involved in the pathophysiology of chronic pain. However, the mechanisms of BDNF action on specific neuronal populations in the spinal superficial dorsal horn (SDH) requires further study. We used chronic BDNF treatment (200 ng/ml, 5–6 days) of defined-medium, serum-free spinal organotypic cultures to study intracellular calcium ([Ca(2+)](i)) fluctuations. A detailed quantitative analysis of these fluctuations using the Frequency-independent biological signal identification (FIBSI) program revealed that BDNF simultaneously depressed activity in some SDH neurons while it unmasked a particular subpopulation of ‘silent’ neurons causing them to become spontaneously active. Blockade of gap junctions disinhibited a subpopulation of SDH neurons and reduced BDNF-induced synchrony in BDNF-treated cultures. BDNF reduced neuronal excitability assessed by measuring spontaneous excitatory postsynaptic currents. This was similar to the depressive effect of BDNF on the [Ca(2+)](i) fluctuations. This study reveals novel regulatory mechanisms of SDH neuronal excitability in response to BDNF. Nature Publishing Group UK 2021-01-26 /pmc/articles/PMC7838274/ /pubmed/33500423 http://dx.doi.org/10.1038/s41598-021-81269-6 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Alles, Sascha R. A.
Odem, Max A.
Lu, Van B.
Cassidy, Ryan M.
Smith, Peter A.
Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
title Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
title_full Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
title_fullStr Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
title_full_unstemmed Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
title_short Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
title_sort chronic bdnf simultaneously inhibits and unmasks superficial dorsal horn neuronal activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838274/
https://www.ncbi.nlm.nih.gov/pubmed/33500423
http://dx.doi.org/10.1038/s41598-021-81269-6
work_keys_str_mv AT allessaschara chronicbdnfsimultaneouslyinhibitsandunmaskssuperficialdorsalhornneuronalactivity
AT odemmaxa chronicbdnfsimultaneouslyinhibitsandunmaskssuperficialdorsalhornneuronalactivity
AT luvanb chronicbdnfsimultaneouslyinhibitsandunmaskssuperficialdorsalhornneuronalactivity
AT cassidyryanm chronicbdnfsimultaneouslyinhibitsandunmaskssuperficialdorsalhornneuronalactivity
AT smithpetera chronicbdnfsimultaneouslyinhibitsandunmaskssuperficialdorsalhornneuronalactivity