Literature DB >> 2207681

Properties of nociceptive and non-nociceptive neurons in trigeminal subnucleus oralis of the rat.

R Dallel1, P Raboisson, A Woda, B J Sessle.   

Abstract

Recent studies have provided evidence suggesting the involvement of rostral components of the V brainstem complex such as trigeminal (V) subnucleus oralis in orofacial pain mechanisms. Since there has been no detailed investigation of the possible existence of nociceptive oralis neurons in the rat to substantiate this recent evidence, the present study was initiated to determine if neurons responsive to noxious orofacial stimuli were present in subnucleus oralis and to characterize their functional properties. In anesthetized rats, recordings were made of the extracellular activity of single neurons functionally characterized as low-threshold mechanoreceptive (LTM), wide dynamic range (WDR) or nociceptive-specific (NS) neurons. The 342 LTM neurons responded only to light mechanical stimulation of orofacial tissues. The mechanoreceptive field of the LTM neurons included the intraoral region in 28% and was localized to the adjacent perioral area in 65%. For 95% the field was localized within one V division. Responses evoked in LTM neurons by electrical stimulation of the orofacial mechanoreceptive field revealed A fiber afferent inputs but no activity that could be attributed to C fiber afferent inputs. The 72 nociceptive neurons included 52 WDR neurons which responded to light (e.g. tactile) as well as noxious (e.g. heavy pressure; pinch) mechanical stimulation of perioral cutaneous and intraoral structures, and 20 NS neurons which responded exclusively to noxious mechanical stimuli. They also differed from the LTM neurons in that 36% of the WDR and 20% of the NS neurons had a mechanoreceptive field involving more than one V division. However, in accordance with our findings for the LTM neurons, the majority of WDR and NS neurons had a mechanoreceptive field involving the intraoral and perioral representations of the mandibular and/or maxillary divisions; those neurons having a mandibular field which especially included intraoral structures predominated in the dorsomedial zone of subnucleus oralis whereas those with a perioral mechanoreceptive field which particularly involved the maxillary division were concentrated in the ventrolateral zone of oralis. In contrast to the LTM neurons, 57% of the WDR and 67% of the NS neurons showed evidence of electrically evoked C fiber as well as A fiber afferent inputs from their mechanoreceptive field. We also noted suppression of the electrically evoked responses by heating of the tail or pinching of the paw. This effect was considered to be a reflection of diffuse noxious inhibitory controls, and was seen in NS as well as WDR neurons; most, but not all, of these neurons received A fiber as well as C fiber orofacial afferent inputs.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2207681     DOI: 10.1016/0006-8993(90)91529-p

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  14 in total

1.  Ultrastructure of the main sensory nucleus of the trigeminal nerve of the cat in normal conditions and in conditions of threshold pain stimulation.

Authors:  G I Kiknadze; E I Dzamoeva; I L Lazriev
Journal:  Neurosci Behav Physiol       Date:  2001 Nov-Dec

2.  Identification of c-Fos immunoreactive brainstem neurons activated during fictive mastication in the rabbit.

Authors:  T Athanassiadis; K A Olsson; A Kolta; K-G Westberg
Journal:  Exp Brain Res       Date:  2005-05-11       Impact factor: 1.972

Review 3.  The role of sensory fiber demography in trigeminal and postherpetic neuralgias.

Authors:  A F DaSilva; M F DosSantos
Journal:  J Dent Res       Date:  2011-06-13       Impact factor: 6.116

4.  Morphine administered in the substantia gelatinosa of the spinal trigeminal nucleus caudalis inhibits nociceptive activities in the spinal trigeminal nucleus oralis.

Authors:  R Dallel; C Dualé; J L Molat
Journal:  J Neurosci       Date:  1998-05-15       Impact factor: 6.167

5.  Neurobiological and psychophysical mechanisms underlying the oral sensation produced by carbonated water.

Authors:  C T Simons; J M Dessirier; M I Carstens; M O'Mahony; E Carstens
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

6.  Persistent facial pain increases superoxide anion production in the spinal trigeminal nucleus.

Authors:  Emanuela Viggiano; Marcellino Monda; Alessandro Viggiano; Andrea Viggiano; Caterina Aurilio; Bruno De Luca
Journal:  Mol Cell Biochem       Date:  2010-01-08       Impact factor: 3.396

7.  Differential activation of the human trigeminal nuclear complex by noxious and non-noxious orofacial stimulation.

Authors:  Paul G Nash; Vaughan G Macefield; Iven J Klineberg; Greg M Murray; Luke A Henderson
Journal:  Hum Brain Mapp       Date:  2009-11       Impact factor: 5.038

8.  Central connectivity of transient receptor potential melastatin 8-expressing axons in the brain stem and spinal dorsal horn.

Authors:  Yun Sook Kim; Jun Hong Park; Su Jung Choi; Jin Young Bae; Dong Kuk Ahn; David D McKemy; Yong Chul Bae
Journal:  PLoS One       Date:  2014-04-07       Impact factor: 3.240

9.  Mechanisms involved in an increment of multimodal excitability of medullary and upper cervical dorsal horn neurons following cutaneous capsaicin treatment.

Authors:  Kuniya Honda; Junichi Kitagawa; Barry J Sessle; Masahiro Kondo; Yoshiyuki Tsuboi; Yoshiyuki Yonehara; Koichi Iwata
Journal:  Mol Pain       Date:  2008-11-19       Impact factor: 3.395

10.  Glycine inhibitory dysfunction turns touch into pain through PKCgamma interneurons.

Authors:  Loïs S Miraucourt; Radhouane Dallel; Daniel L Voisin
Journal:  PLoS One       Date:  2007-11-07       Impact factor: 3.240

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