Literature DB >> 28458040

Temporal and spatial dynamics of peripheral afferent-evoked activity in the dorsal horn recorded in rat spinal cord slices.

Fang Yu1, Zhen-Yu Zhao2, Ting He3, Yao-Qing Yu3, Zhen Li3, Jun Chen4.   

Abstract

In the present study, multi-electrode array recording was used to examine dorsal horn activity following stimulation of primary afferents in a rat dorsal root attached-spinal cord slice preparation. The multi-electrode array probe was placed under the dorsal horn slice and local field potentials evoked by stimulation on the dorsal root were analyzed. Three kinds of dorsal root-evoked responses were identified. In lamina IIo, local field potentials exhibited P1 (peak latency 1.46±0.08ms), N1 (2.77±0.18ms, n=12), N2 (7.31±0.48ms), N3 (12.12±0.73ms) and P2(18.30±0.80ms) waves. In lamina IIi local field potentials exhibited P (1.99±0.10ms), N1 (3.35±0.17ms) and N2 (8.58±0.44ms) waves. In laminae III-VI, local field potentials exhibited P1 (3.01±0.07ms), P2 (7.02±0.21ms) and N waves (22.57±0.79ms). Sweep spread was calculated by two dimensional current source density (2D-CSD) analysis. Both α-amino-3-hydroxy-5-methylisoxazole-4-propionic a/kainate and N-methyl-d-aspartate-type glutamate receptors participated in this neuronal circuitry. Morphine diminished local field potentials. Gabapentin diminished the negative components in lamina II and P2 component in lamina IIo, but increased the positive components in lamina IIi and laminae III-VI. The present study revealed that functional dorsal horn activity was preserved in the spinal cord slice preparation. Glutamatergic synapses were crucially involved in information processing. Opioid interneurons and gabapentin may play a modulatory role in regulating signal flows in the dorsal horn. Taken together, these results identify a spatio-temporal profile of dorsal horn activity evoked by dorsal root stimulation, and implicate glutamatergic and opioidergic receptors and gabapentin in this activity.
Copyright © 2017. Published by Elsevier Inc.

Entities:  

Keywords:  Current source density; Multi-electrode array; Nociceptive circuitry; Primary afferent; Spinal dorsal horn

Mesh:

Substances:

Year:  2017        PMID: 28458040     DOI: 10.1016/j.brainresbull.2017.04.012

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  2 in total

1.  Ceftriaxone Relieves Trigeminal Neuropathic Pain Through Suppression of Spatiotemporal Synaptic Plasticity via Restoration of Glutamate Transporter 1 in the Medullary Dorsal Horn.

Authors:  Xiao Luo; Ting He; Yan Wang; Jiang-Lin Wang; Xue-Bin Yan; Hao-Cheng Zhou; Rui-Rui Wang; Rui Du; Xiao-Liang Wang; Jun Chen; Dong Huang
Journal:  Front Cell Neurosci       Date:  2020-06-30       Impact factor: 5.505

2.  Calretinin positive neurons form an excitatory amplifier network in the spinal cord dorsal horn.

Authors:  Christopher V Dayas; David I Hughes; Brett A Graham; Kelly M Smith; Tyler J Browne; Olivia C Davis; A Coyle; Kieran A Boyle; Masahiko Watanabe; Sally A Dickinson; Jacqueline A Iredale; Mark A Gradwell; Phillip Jobling; Robert J Callister
Journal:  Elife       Date:  2019-11-12       Impact factor: 8.140

  2 in total

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