Literature DB >> 10526107

Evidence for subnucleus interpolaris in craniofacial muscle pain mechanisms demonstrated by intramuscular injections with hypertonic saline.

J Y Ro1, N F Capra.   

Abstract

The subnucleus interpolaris (Vi) has been identified as a major recipient for trigeminal ganglionic input from jaw muscles, and contains neurons with nociceptive properties similar to those in the subnucleus caudalis (Vc). Therefore, Vi may be another important site for processing craniofacial muscle nociception. The aims of present study were to define functional properties of Vi neurons that receive input from masseter muscle afferents by characterizing their responses to electrical, mechanical, and to chemical stimulation of the muscle. Ninety cells were identified as masseter muscle units in 11 adult cats. Most of these units (79%) received additional inputs from orofacial skin. Following the intramuscular injection of 5% hypertonic saline, 49% of the cells showed a significant modulation of either the resting discharge and/or responses to innocuous mechanical stimulation on their cutaneous receptive fields (RFs). The most common response to saline injection was an induction or facilitation of resting discharge which declined as an exponential decay function, returning to pre-injection level within 3-4 min. Forty-five percent of the muscle units that were tested with mechanical stimulation (13/29) showed a prolonged inhibition of mechanically-evoked responses. In most cases (8/13), the inhibitory response was accompanied by initial facilitation. The observations that Vi contained a population of neurons that receive small diameter muscle afferent inputs, responded to noxious mechanical stimulation on the muscle and to a chemical irritant that is known to produce pain in humans provide compelling evidence for the involvement of Vi in craniofacial muscle pain mechanisms.

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Year:  1999        PMID: 10526107     DOI: 10.1016/s0006-8993(99)01860-0

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


  6 in total

1.  Experimental skin pain and muscle pain induce distinct changes in human trigeminal motoneuronal excitability.

Authors:  A Truini; A Romaniello; P Svensson; F Galeotti; T Graven-Nielsen; K Wang; G Cruccu; L Arendt-Nielsen
Journal:  Exp Brain Res       Date:  2006-05-30       Impact factor: 1.972

2.  Targeted ablation of mesenteric projecting sympathetic neurons reduces the hemodynamic response to pain in conscious, spinal cord-transected rats.

Authors:  Heidi L Lujan; Gurunanthan Palani; Jean D Peduzzi; Stephen E DiCarlo
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-03-10       Impact factor: 3.619

3.  Interactions between Pain and the Motor Cortex: Insights from Research on Phantom Limb Pain and Complex Regional Pain Syndrome.

Authors:  Catherine Mercier; Guillaume Léonard
Journal:  Physiother Can       Date:  2011-08-10       Impact factor: 1.037

4.  The influence of pain on masseter spindle afferent discharge.

Authors:  Norman F Capra; Calvin K Hisley; Radi M Masri
Journal:  Arch Oral Biol       Date:  2006-11-28       Impact factor: 2.633

5.  Somatotopic activation in the human trigeminal pain pathway.

Authors:  Alex F M DaSilva; Lino Becerra; Nikos Makris; Andrew M Strassman; R Gilberto Gonzalez; Nina Geatrakis; David Borsook
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

6.  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

  6 in total

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