Literature DB >> 3373275

Descending excitation and inhibition of spinal cord lamina I projection neurons.

S B McMahon1, P D Wall.   

Abstract

1. Lamina I cells were recorded in the lumbar dorsal horn of decerebrate rats. Their projecting axons were mainly located in the contralateral dorsolateral funiculus (DLF) in the upper cervical cord. 2. The effect on these cells of short and long trains of stimuli applied to the upper cervical DLF was examined by measuring the ongoing activity of the cells, their response to peripheral stimuli, and the size of their receptive fields. 3. The presence of tonic descending influences from brain stem to spinal cord was investigated by measuring the properties of the lamina I cells before and during block of descending impulses. 4. The results of DLF stimulation and of cord block show that substantial and prolonged excitation affected many cells, whereas some were inhibited for shorter periods of time. 5. The experiments were repeated with stimulation of the DLF caudal to chronic section to eliminate descending fibers. The results suggest that the changes of excitability in intact animals were partly produced by stimulation of descending fibers and partly by the invasion of collaterals activated by the antidromic stimulation of the axons projecting from the lamina I cells. 6. Although long trains of DLF stimuli generally excited lamina I cells, only inhibitions were seen in the deep dorsal horn. Moreover, stimulation rostral to an acute unilateral DLF lesion was without effect on lamina I cells but inhibited deep cells. 7. It is proposed that the lamina I cells might activate brain stem circuits, which in turn influence deep dorsal horn cells.

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Year:  1988        PMID: 3373275     DOI: 10.1152/jn.1988.59.4.1204

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  8 in total

1.  Supraspinal inhibition of nociceptive dorsal horn neurones in the anaesthetized rat: tonic or dynamic?

Authors:  H S Li; R Monhemius; B A Simpson; M H Roberts
Journal:  J Physiol       Date:  1998-01-15       Impact factor: 5.182

2.  Involvement of cGMP in nociceptive processing by and sensitization of spinothalamic neurons in primates.

Authors:  Q Lin; Y B Peng; J Wu; W D Willis
Journal:  J Neurosci       Date:  1997-05-01       Impact factor: 6.167

3.  Spino-bulbo-spinal pathway mediating vagal modulation of nociceptive-neuroendocrine control of inflammation in the rat.

Authors:  F J Miao; W Jänig; L Jasmin; J D Levine
Journal:  J Physiol       Date:  2001-05-01       Impact factor: 5.182

4.  Anterior pretectal nucleus facilitation of superficial dorsal horn neurones and modulation of deafferentation pain in the rat.

Authors:  H Rees; M G Terenzi; M H Roberts
Journal:  J Physiol       Date:  1995-11-15       Impact factor: 5.182

5.  Inhibition of temporomandibular joint input to medullary dorsal horn neurons by 5HT3 receptor antagonist in female rats.

Authors:  K Okamoto; A Katagiri; M Rahman; R Thompson; D A Bereiter
Journal:  Neuroscience       Date:  2015-04-23       Impact factor: 3.590

6.  Estrogen status and psychophysical stress modify temporomandibular joint input to medullary dorsal horn neurons in a lamina-specific manner in female rats.

Authors:  Keiichiro Okamoto; Randall Thompson; Ayano Katagiri; David A Bereiter
Journal:  Pain       Date:  2013-03-15       Impact factor: 6.961

7.  A spinoparabrachial circuit defined by Tacr1 expression drives pain.

Authors:  Arnab Barik; Anupama Sathyamurthy; James Thompson; Mathew Seltzer; Ariel Levine; Alexander Chesler
Journal:  Elife       Date:  2021-02-16       Impact factor: 8.140

8.  Sensitization of lamina I spinoparabrachial neurons parallels heat hyperalgesia in the chronic constriction injury model of neuropathic pain.

Authors:  David Andrew
Journal:  J Physiol       Date:  2009-03-16       Impact factor: 5.182

  8 in total

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