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Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain
Arterial spin labelling (ASL) plays an increasingly important role in neuroimaging pain research but does not provide molecular insights regarding how regional cerebral blood flow (rCBF) relates to underlying neurotransmission. Here, we integrate ASL with positron emission tomography (PET) and brain...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812236/ https://www.ncbi.nlm.nih.gov/pubmed/35796178 http://dx.doi.org/10.1002/hbm.25999 |
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author | Vamvakas, Alexandros Lawn, Timothy Veronese, Mattia Williams, Steven C. R. Tsougos, Ioannis Howard, Matthew A. |
author_facet | Vamvakas, Alexandros Lawn, Timothy Veronese, Mattia Williams, Steven C. R. Tsougos, Ioannis Howard, Matthew A. |
author_sort | Vamvakas, Alexandros |
collection | PubMed |
description | Arterial spin labelling (ASL) plays an increasingly important role in neuroimaging pain research but does not provide molecular insights regarding how regional cerebral blood flow (rCBF) relates to underlying neurotransmission. Here, we integrate ASL with positron emission tomography (PET) and brain transcriptome data to investigate the molecular substrates of rCBF underlying clinically relevant pain states. Two data sets, representing acute and chronic ongoing pain respectively, were utilised to quantify changes in rCBF; one examining pre‐surgical versus post‐surgical pain, and the second comparing patients with painful hand Osteoarthritis to a group of matched controls. We implemented a whole‐brain spatial correlation analysis to explore associations between change in rCBF (ΔCBF) and neurotransmitter receptor distributions derived from normative PET templates. Additionally, we utilised transcriptomic data from the Allen Brain Atlas to inform distributions of receptor expression. Both datasets presented significant correlations of ΔCBF with the μ‐opioid and dopamine‐D2 receptor expressions, which play fundamental roles in brain activity associated with pain experiences. ΔCBF also correlated with the gene expression distributions of several receptors involved in pain processing. Overall, this is the first study illustrating the molecular basis of ongoing pain ASL indices and emphasises the potential of rCBF as a biomarker in pain research. |
format | Online Article Text |
id | pubmed-9812236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98122362023-01-05 Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain Vamvakas, Alexandros Lawn, Timothy Veronese, Mattia Williams, Steven C. R. Tsougos, Ioannis Howard, Matthew A. Hum Brain Mapp Research Articles Arterial spin labelling (ASL) plays an increasingly important role in neuroimaging pain research but does not provide molecular insights regarding how regional cerebral blood flow (rCBF) relates to underlying neurotransmission. Here, we integrate ASL with positron emission tomography (PET) and brain transcriptome data to investigate the molecular substrates of rCBF underlying clinically relevant pain states. Two data sets, representing acute and chronic ongoing pain respectively, were utilised to quantify changes in rCBF; one examining pre‐surgical versus post‐surgical pain, and the second comparing patients with painful hand Osteoarthritis to a group of matched controls. We implemented a whole‐brain spatial correlation analysis to explore associations between change in rCBF (ΔCBF) and neurotransmitter receptor distributions derived from normative PET templates. Additionally, we utilised transcriptomic data from the Allen Brain Atlas to inform distributions of receptor expression. Both datasets presented significant correlations of ΔCBF with the μ‐opioid and dopamine‐D2 receptor expressions, which play fundamental roles in brain activity associated with pain experiences. ΔCBF also correlated with the gene expression distributions of several receptors involved in pain processing. Overall, this is the first study illustrating the molecular basis of ongoing pain ASL indices and emphasises the potential of rCBF as a biomarker in pain research. John Wiley & Sons, Inc. 2022-07-07 /pmc/articles/PMC9812236/ /pubmed/35796178 http://dx.doi.org/10.1002/hbm.25999 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Vamvakas, Alexandros Lawn, Timothy Veronese, Mattia Williams, Steven C. R. Tsougos, Ioannis Howard, Matthew A. Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain |
title | Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain |
title_full | Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain |
title_fullStr | Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain |
title_full_unstemmed | Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain |
title_short | Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain |
title_sort | neurotransmitter receptor densities are associated with changes in regional cerebral blood flow during clinical ongoing pain |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812236/ https://www.ncbi.nlm.nih.gov/pubmed/35796178 http://dx.doi.org/10.1002/hbm.25999 |
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