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Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn

Parvalbumin-expressing interneurons (PVINs) in the spinal dorsal horn are found primarily in laminae II inner and III. Inhibitory PVINs play an important role in segregating innocuous tactile input from pain-processing circuits through presynaptic inhibition of myelinated low-threshold mechanorecept...

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Detalles Bibliográficos
Autores principales: Gradwell, Mark A., Boyle, Kieran A., Browne, Tyler J., Bell, Andrew M., Leonardo, Jacklyn, Peralta Reyes, Fernanda S., Dickie, Allen C., Smith, Kelly M., Callister, Robert J., Dayas, Christopher V., Hughes, David I., Graham, Brett A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832545/
https://www.ncbi.nlm.nih.gov/pubmed/34326298
http://dx.doi.org/10.1097/j.pain.0000000000002422
Descripción
Sumario:Parvalbumin-expressing interneurons (PVINs) in the spinal dorsal horn are found primarily in laminae II inner and III. Inhibitory PVINs play an important role in segregating innocuous tactile input from pain-processing circuits through presynaptic inhibition of myelinated low-threshold mechanoreceptors and postsynaptic inhibition of distinct spinal circuits. By comparison, relatively little is known of the role of excitatory PVINs (ePVINs) in sensory processing. Here, we use neuroanatomical and optogenetic approaches to show that ePVINs comprise a larger proportion of the PVIN population than previously reported and that both ePVIN and inhibitory PVIN populations form synaptic connections among (and between) themselves. We find that these cells contribute to neuronal networks that influence activity within several functionally distinct circuits and that aberrant activity of ePVINs under pathological conditions is well placed to contribute to the development of mechanical hypersensitivity.