Literature DB >> 15733646

Differential modulation of TMJ neurons in superficial laminae of trigeminal subnucleus caudalis/upper cervical cord junction region of male and cycling female rats by morphine.

K Okamoto1, A Tashiro, H Hirata, D A Bereiter.   

Abstract

Sex differences in the cellular responses to morphine were examined in an animal model of temporomandibular joint (TMJ) pain. TMJ-responsive neurons were recorded in the superficial laminae at the trigeminal subnucleus caudalis/upper cervical cord (Vc/C(2)) junction region, the initial site of synaptic integration for TMJ afferents, in male and cycling female rats under barbiturate anesthesia. Unit activity was evoked by local injection of bradykinin into the TMJ capsule at 30 min intervals and the effects of morphine sulfate (0.03-3 mg/kg, i.v.) were assessed by a cumulative dose regimen. Morphine caused a dose-related inhibition of bradykinin-evoked unit activity in males and diestrous females in a naloxone-reversible manner, while evoked unit activity in proestrous females was not reduced. The apparent sex hormone-related aspect of morphine analgesia was selective for evoked unit activity, since the spontaneous activity of TMJ units was reduced similarly in all groups, while the convergent cutaneous receptive field area of TMJ units did not change in any group. These results were consistent with the hypothesis that sex hormone status interacts with pain control systems to modify neural activity at the level of the Vc/C(2) junction region relevant for TMD pain.

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Year:  2005        PMID: 15733646     DOI: 10.1016/j.pain.2004.12.013

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


  9 in total

1.  Sex differences in lumbar spinal cord gene expression following experimental lumbar radiculopathy.

Authors:  Michael L LaCroix-Fralish; Vivianne L Tawfik; Kevin F Spratt; Joyce A DeLeo
Journal:  J Mol Neurosci       Date:  2006       Impact factor: 3.444

2.  Sex differences in micro-opioid receptor expression in the rat midbrain periaqueductal gray are essential for eliciting sex differences in morphine analgesia.

Authors:  Dayna R Loyd; Xioaya Wang; Anne Z Murphy
Journal:  J Neurosci       Date:  2008-12-24       Impact factor: 6.167

3.  NMDA receptor blockade reduces temporomandibular joint-evoked activity of trigeminal subnucleus caudalis neurons in an estrogen-dependent manner.

Authors:  A Tashiro; K Okamoto; D A Bereiter
Journal:  Neuroscience       Date:  2009-09-30       Impact factor: 3.590

4.  Morphine preferentially activates the periaqueductal gray-rostral ventromedial medullary pathway in the male rat: a potential mechanism for sex differences in antinociception.

Authors:  D R Loyd; M M Morgan; A Z Murphy
Journal:  Neuroscience       Date:  2007-05-31       Impact factor: 3.590

Review 5.  Neuronal and glial factors contributing to sex differences in opioid modulation of pain.

Authors:  Dayna L Averitt; Lori N Eidson; Hillary H Doyle; Anne Z Murphy
Journal:  Neuropsychopharmacology       Date:  2018-06-23       Impact factor: 7.853

6.  Examination of sex and minocycline treatment on acute morphine-induced analgesia and inflammatory gene expression along the pain pathway in Sprague-Dawley rats.

Authors:  Caitlin K Posillico; Laurne S Terasaki; Staci D Bilbo; Jaclyn M Schwarz
Journal:  Biol Sex Differ       Date:  2015-12-12       Impact factor: 5.027

7.  Ablation of spinal cord estrogen receptor α-expressing interneurons reduces chemically induced modalities of pain and itch.

Authors:  May Tran; Joao Manuel Braz; Katherine Hamel; Julia Kuhn; Andrew J Todd; Allan I Basbaum
Journal:  J Comp Neurol       Date:  2020-01-06       Impact factor: 3.028

Review 8.  The role of the periaqueductal gray in the modulation of pain in males and females: are the anatomy and physiology really that different?

Authors:  Dayna R Loyd; Anne Z Murphy
Journal:  Neural Plast       Date:  2009-01-28       Impact factor: 3.599

9.  Release of glutamate and CGRP from trigeminal ganglion neurons: Role of calcium channels and 5-HT1 receptor signaling.

Authors:  Yan Xiao; Judith A Richter; Joyce H Hurley
Journal:  Mol Pain       Date:  2008-04-16       Impact factor: 3.395

  9 in total

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