Literature DB >> 15604230

In vivo responses of mouse superficial dorsal horn neurones to both current injection and peripheral cutaneous stimulation.

B A Graham1, A M Brichta, R J Callister.   

Abstract

In the superficial dorsal horn (SDH) processing of noxious and innocuous stimuli is critically dependent on the input-output relationship of its component neurones. Such relationships are routinely examined by assessing neuronal responses to somatic current injection or activation of synaptic inputs. A more complete understanding of input-output relationships would be achieved by comparing, in the same neurone, how the two forms of activation contribute to neuronal output. Therefore, we examined how SDH neurones transform depolarizing current injections and synaptic excitation via peripheral cutaneous stimuli (brush and pinch of the hindpaw) into trains of action potentials, in an in vivo preparation of the adult mouse spinal cord. Under whole-cell current clamp recording conditions four action potential discharge patterns were observed during depolarizing current injection: tonic firing neurones (21/93) discharged spikes throughout the step; initial bursting neurones (35/93) discharged several spikes at step onset; single spiking neurones (16/93) discharged one or two spikes at step onset; and delayed firing neurones (21/93) discharged spikes delayed from the step onset. Four characteristic profiles were observed in response to application of noxious (pinch) and innocuous (brush) cutaneous stimuli: nociceptive neurones (20/37) responded maximally to pinch stimulation; light touch neurones (9/37) responded maximally to brush stimulation; subthreshold neurones (4/37) exhibited depolarizing responses without firing action potentials; and hyperpolarizing neurones (4/37) exhibited a sustained pinch-induced hyperpolarization. Comparisons of current-evoked discharge patterns with peripherally evoked responses indicate SDH neurones expressing each of the four discharge patterns could receive, and therefore participate in the processing of information concerning, either noxious or innocuous stimuli. These data suggest that a neurone's response to current injection does not necessarily help identify or predict how the same neurone will respond to physiologically or functionally relevant stimuli.

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Year:  2004        PMID: 15604230      PMCID: PMC1665382          DOI: 10.1113/jphysiol.2004.072645

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  44 in total

1.  Responsiveness of rat substantia gelatinosa neurones to mechanical but not thermal stimuli revealed by in vivo patch-clamp recording.

Authors:  H Furue; K Narikawa; E Kumamoto; M Yoshimura
Journal:  J Physiol       Date:  1999-12-01       Impact factor: 5.182

2.  In vivo patch-clamp analysis of IPSCs evoked in rat substantia gelatinosa neurons by cutaneous mechanical stimulation.

Authors:  K Narikawa; H Furue; E Kumamoto; M Yoshimura
Journal:  J Neurophysiol       Date:  2000-10       Impact factor: 2.714

3.  Correlations between neuronal morphology and electrophysiological features in the rodent superficial dorsal horn.

Authors:  T J Grudt; E R Perl
Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

4.  Morphological and physiological features of a set of spinal substantia gelatinosa neurons defined by green fluorescent protein expression.

Authors:  Adam W Hantman; Anthony N van den Pol; Edward R Perl
Journal:  J Neurosci       Date:  2004-01-28       Impact factor: 6.167

5.  An in vivo mouse spinal cord preparation for patch-clamp analysis of nociceptive processing.

Authors:  B A Graham; A M Brichta; R J Callister
Journal:  J Neurosci Methods       Date:  2004-07-30       Impact factor: 2.390

6.  Central projections of identified, unmyelinated (C) afferent fibers innervating mammalian skin.

Authors:  Y Sugiura; C L Lee; E R Perl
Journal:  Science       Date:  1986-10-17       Impact factor: 47.728

7.  Spinal neurons specifically excited by noxious or thermal stimuli: marginal zone of the dorsal horn.

Authors:  B N Christensen; E R Perl
Journal:  J Neurophysiol       Date:  1970-03       Impact factor: 2.714

8.  Physiology and morphology of substantia gelatinosa neurons intracellularly stained with horseradish peroxidase.

Authors:  G J Bennett; M Abdelmoumene; H Hayashi; R Dubner
Journal:  J Comp Neurol       Date:  1980-12-15       Impact factor: 3.215

Review 9.  The localization of classical transmitters and neuropeptides within neurons in laminae I-III of the mammalian spinal dorsal horn.

Authors:  A J Todd; R C Spike
Journal:  Prog Neurobiol       Date:  1993-11       Impact factor: 11.685

Review 10.  A comparative study of the calcium-binding proteins calbindin-D28K, calretinin, calmodulin and parvalbumin in the rat spinal cord.

Authors:  K Ren; M A Ruda
Journal:  Brain Res Brain Res Rev       Date:  1994-05
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  46 in total

1.  Circuit breaking the synaptic connections of the superficial dorsal horn of the spinal cord.

Authors:  David Andrew
Journal:  J Physiol       Date:  2010-07-01       Impact factor: 5.182

2.  Afterhyperpolarization-firing rate relation of turtle spinal neurons.

Authors:  E K Stauffer; D G Stuart; J C McDonagh; T G Hornby; R M Reinking
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2004-12-10       Impact factor: 1.836

3.  Measurement and nature of firing rate adaptation in turtle spinal neurons.

Authors:  R B Gorman; J C McDonagh; T G Hornby; R M Reinking; D G Stuart
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2005-05-20       Impact factor: 1.836

4.  Properties of mouse spinal lamina I GABAergic interneurons.

Authors:  Kimberly J Dougherty; Michael A Sawchuk; Shawn Hochman
Journal:  J Neurophysiol       Date:  2005-07-13       Impact factor: 2.714

5.  Pinch-current injection defines two discharge profiles in mouse superficial dorsal horn neurones, in vitro.

Authors:  B A Graham; A M Brichta; R J Callister
Journal:  J Physiol       Date:  2006-11-23       Impact factor: 5.182

Review 6.  Historical reflections on the afterhyperpolarization--firing rate relation of vertebrate spinal neurons.

Authors:  E K Stauffer; J C McDonagh; T G Hornby; R M Reinking; D G Stuart
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2006-12-28       Impact factor: 1.836

7.  Excitatory interneurons dominate sensory processing in the spinal substantia gelatinosa of rat.

Authors:  Sónia F A Santos; Sandra Rebelo; Victor A Derkach; Boris V Safronov
Journal:  J Physiol       Date:  2007-03-01       Impact factor: 5.182

8.  Analysis of spontaneous activity of superficial dorsal horn neurons in vitro: neuropathy-induced changes.

Authors:  Carolina Roza; Irene Mazo; Iván Rivera-Arconada; Elsa Cisneros; Ismel Alayón; José A López-García
Journal:  Pflugers Arch       Date:  2016-10-10       Impact factor: 3.657

9.  Dissociation of μ- and δ-opioid inhibition of glutamatergic synaptic transmission in superficial dorsal horn.

Authors:  Paul J Wrigley; Hyo-Jin Jeong; Christopher W Vaughan
Journal:  Mol Pain       Date:  2010-10-26       Impact factor: 3.395

10.  Persistent inward currents in rat ventral horn neurones.

Authors:  Renée D Theiss; Jason J Kuo; C J Heckman
Journal:  J Physiol       Date:  2007-02-08       Impact factor: 5.182

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