Literature DB >> 3226758

Effects of lesions to rat spinal cord lamina I cell projection pathways on reactions to acute and chronic noxious stimuli.

P D Wall1, J Bery, N Saadé.   

Abstract

(1) Lamina I contains large numbers of nociceptive specific cells and wide-dynamic-range (WDR) cells which respond to both noxious and innocuous stimuli. Many of the cells project to the brain. 82% of the projecting axons travel by way of the contralateral dorsolateral funiculus (DLF). (2) Section of the contralateral DLF produced no change in behavioural response to brief mechanical or thermal or chemical stimuli. However, section of the contralateral DLF greatly accelerated the slow onset autotomy in response to section of the sciatic and saphenous nerves. (3) Section of the ipsilateral DLF or bilateral section produce the same acceleration of onset of autotomy as is produced by contralateral DLF section. Section of dorsal columns does not change the long-term onset of autotomy. (4) Destruction of cells with ibotenic acid in the contralateral parabrachial area where many lamina I cells are known to terminate produced the same acceleration of autotomy as was observed after DLF lesions. Contralateral cortical lesions were without effect on autotomy. (5) It is proposed that the lamina I projection system is more concerned with long-latency long-duration reactions to prolonged events than to abrupt reactions to brief stimuli. The behavioural results reported here are consistent with McMahon and Wall's physiological hypothesis that a contralateral DLF projecting pathway excites cells in the parabrachial area which in turn excite descending control systems running mainly in the ipsilateral DLF to affect spinal dorsal horn cells.

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Year:  1988        PMID: 3226758     DOI: 10.1016/0304-3959(88)90142-X

Source DB:  PubMed          Journal:  Pain        ISSN: 0304-3959            Impact factor:   6.961


  6 in total

1.  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

2.  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

3.  The role of the dorsolateral funiculi in the pain relieving effect of spinal cord stimulation: a study in a rat model of neuropathic pain.

Authors:  N E Saadé; J Barchini; S Tchachaghian; F Chamaa; S J Jabbur; Z Song; B A Meyerson; B Linderoth
Journal:  Exp Brain Res       Date:  2014-12-24       Impact factor: 1.972

4.  Hyperalgesia and sensitization of dorsal horn neurons following activation of NK-1 receptors in the rostral ventromedial medulla.

Authors:  Sergey G Khasabov; Patrick Malecha; Joseph Noack; Janneta Tabakov; Glenn J Giesler; Donald A Simone
Journal:  J Neurophysiol       Date:  2017-08-09       Impact factor: 2.714

5.  Nonviral retrograde gene transfer of human hepatocyte growth factor improves neuropathic pain-related phenomena in rats.

Authors:  Toyokazu Tsuchihara; Sho Ogata; Koichi Nemoto; Takatoshi Okabayashi; Kuniaki Nakanishi; Naoki Kato; Ryuichi Morishita; Yasufumi Kaneda; Maki Uenoyama; Shinya Suzuki; Masatoshi Amako; Toshiaki Kawai; Hiroshi Arino
Journal:  Mol Ther       Date:  2008-10-21       Impact factor: 11.454

6.  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

  6 in total

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