Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/138985
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dc.creatorAgashkov, K
dc.creatorKrotov, V
dc.creatorKrasniakova, M
dc.creatorShevchuk, D
dc.creatorAndrianov, Y
dc.creatorZabenko, Y
dc.creatorSafronov, BV
dc.creatorVoitenko, N
dc.creatorBelan, P
dc.date.accessioned2022-01-10T09:58:51Z-
dc.date.available2022-01-10T09:58:51Z-
dc.date.issued2019
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/10216/138985-
dc.description.abstractLamina I spino-parabrachial neurons (SPNs) receive peripheral nociceptive input, process it and transmit to the supraspinal centres. Although responses of SPNs to cutaneous receptive field stimulations have been intensively studied, the mechanisms of signal processing in these neurons are poorly understood. Therefore, we used an ex-vivo spinal cord preparation to examine synaptic and cellular mechanisms determining specific input-output characteristics of the neurons. The vast majority of the SPNs received a few direct nociceptive C-fiber inputs and generated one spike in response to saturating afferent stimulation, thus functioning as simple transducers of painful stimulus. However, 69% of afferent stimulation-induced action potentials in the entire SPN population originated from a small fraction (19%) of high-output neurons. These neurons received a larger number of direct Ad- and C-fiber inputs, generated intrinsic bursts and efficiently integrated a local network activity via NMDA-receptor-dependent mechanisms. The high-output SPNs amplified and integrated the nociceptive input gradually encoding its intensity into the number of generated spikes. Thus, different mechanisms of signal processing allow lamina I SPNs to play distinct roles in nociception.
dc.description.sponsorshipThe authors thank Mr. Andrew Dromaretsky for the technical assistance. P.B. was supported by the National Academy of Sciences of Ukraine (NASU), grant NASU # 0116U004470, grant NASU#67/15-Н. N.V. was supported by the NASU Biotechnology and NASU-KNU grants; NIH 1R01NS113189-01. B.V.S. was supported by the FEDER funds through the COMPETE 2020 (POCI), Portugal 2020, and by the FCT project PTDC/NEU-NMC/1259/2014 (POCI-01-0145-FEDER-016588)
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofScientific Reports, vol.9(1):19231
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.meshAction Potentials / physiology
dc.subject.meshAnimals
dc.subject.meshExcitatory Postsynaptic Potentials / physiology
dc.subject.meshNerve Fibers, Unmyelinated / physiology
dc.subject.meshNeurons / cytology
dc.subject.meshNeurons / physiology
dc.subject.meshNociception / physiology
dc.subject.meshRats
dc.subject.meshRats, Wistar
dc.subject.meshSpinal Cord / cytology
dc.subject.meshSpinal Cord / physiology
dc.subject.meshSynapses / physiology
dc.titleDistinct mechanisms of signal processing by lamina I spino-parabrachial neurons
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1038/s41598-019-55462-7
dc.relation.publisherversionhttps://www.nature.com/articles/s41598-019-55462-7
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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