A nociceptive neuronal ensemble in the dorsomedial prefrontal cortex underlies pain chronicity
Cell Reports, ISSN: 2211-1247, Vol: 41, Issue: 11, Page: 111833
2022
- 22Citations
- 37Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations22
- Citation Indexes22
- 22
- CrossRef10
- Captures37
- Readers37
- 37
Article Description
Pain chronicity involves unpleasant experience in both somatosensory and affective aspects, accompanied with the prefrontal cortex (PFC) neuroplastic alterations. However, whether specific PFC neuronal ensembles underlie pain chronicity remains elusive. Here we identify a nociceptive neuronal ensemble in the dorsomedial prefrontal cortex (dmPFC), which shows prominent reactivity to nociceptive stimuli. We observed that this ensemble shows distinct molecular characteristics and is densely connected to pain-related regions including basolateral amygdala (BLA) and lateral parabrachial nuclei (LPB). Prolonged chemogenetic activation of this nociceptive neuronal ensemble, but not a randomly transfected subset of dmPFC neurons, induces chronic pain-like behaviors in normal mice. By contrast, silencing the nociceptive dmPFC neurons relieves both pain hypersensitivity and anxiety in mice with chronic inflammatory pain. These results suggest the presence of specific dmPFC neuronal ensembles in processing nociceptive information and regulating pain chronicity.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2211124722017259; http://dx.doi.org/10.1016/j.celrep.2022.111833; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85144029281&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36516746; https://linkinghub.elsevier.com/retrieve/pii/S2211124722017259; https://dx.doi.org/10.1016/j.celrep.2022.111833
Elsevier BV
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