Literature DB >> 10482736

Electrophysiological assessment of the cutaneous arborization of Adelta-fiber nociceptors.

Y B Peng1, M Ringkamp, J N Campbell, R A Meyer.   

Abstract

Little is known about the relationship between the branching structure and function of physiologically identified cutaneous nociceptor terminals. The axonal arborization itself, however, has an impact on the afferent signal that is conveyed along the parent axon to the CNS. We therefore developed electrophysiological techniques to investigate the branching structure of cutaneous nociceptors. Single-fiber recordings were obtained from physiologically identified nociceptors that innervated the hairy skin of the monkey. Electrodes for transcutaneous stimulation were fixed at two separate locations inside the receptive field. For 32 Adelta-fiber nociceptors, distinct steps in latency of the recorded action potential were observed as the intensity of the transcutaneous electrical stimulus increased, indicating discrete sites for action potential initiation. The number of discrete latencies at each stimulation location ranged from 1 to 9 (3.7 +/- 0. 2; mean +/- SE) and the mean size of the latency step was 9.9 +/- 1. 0 ms (range: 0.4-89.1 ms). For seven Adelta fibers, collision techniques were used to locate the position of the branch point where the daughter fibers that innervated the two locations within the receptive field join the parent axon. To correct for changes in electrical excitability at the peripheral terminals, collision experiments between the two skin locations and between each skin location and a nerve trunk electrode were necessary. Nine branch points were studied in the seven Adelta fibers; the mean propagation time from the action potential initiation site to the branch point was 31 +/- 5 ms corresponding to a distance of 54 +/- 10 mm. Almost half of the daughter branches were unmyelinated. These results demonstrate that collision techniques can be used to study the functional anatomy of physiologically identified nociceptive afferent terminals. Furthermore these results indicate that some nociceptive afferents branch quite proximal to their peripheral receptive field. Occlusion of action potential activity can occur in these long branches such that the shorter branches dominate in the response to natural stimuli.

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Mesh:

Year:  1999        PMID: 10482736     DOI: 10.1152/jn.1999.82.3.1164

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  17 in total

1.  Action potential conduction in the terminal arborisation of nociceptive C-fibre afferents.

Authors:  C Weidner; R Schmidt; M Schmelz; H E Torebjork; H O Handwerker
Journal:  J Physiol       Date:  2003-02-07       Impact factor: 5.182

2.  Estimating nerve excitation thresholds to cutaneous electrical stimulation by finite element modeling combined with a stochastic branching nerve fiber model.

Authors:  Carsten Dahl Mørch; Kristian Hennings; Ole Kæseler Andersen
Journal:  Med Biol Eng Comput       Date:  2011-01-05       Impact factor: 2.602

3.  A role for nociceptive, myelinated nerve fibers in itch sensation.

Authors:  Matthias Ringkamp; Raf J Schepers; Steven G Shimada; Lisa M Johanek; Timothy V Hartke; Jasenka Borzan; Beom Shim; Robert H LaMotte; Richard A Meyer
Journal:  J Neurosci       Date:  2011-10-19       Impact factor: 6.167

4.  Functional interactions between tumor and peripheral nerve: changes in excitability and morphology of primary afferent fibers in a murine model of cancer pain.

Authors:  D M Cain; P W Wacnik; M Turner; G Wendelschafer-Crabb; W R Kennedy; G L Wilcox; D A Simone
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

5.  Capsaicin responses in heat-sensitive and heat-insensitive A-fiber nociceptors.

Authors:  M Ringkamp; Y B Peng; G Wu; T V Hartke; J N Campbell; R A Meyer
Journal:  J Neurosci       Date:  2001-06-15       Impact factor: 6.167

6.  How does morphology relate to function in sensory arbors?

Authors:  David H Hall; Millet Treinin
Journal:  Trends Neurosci       Date:  2011-08-16       Impact factor: 13.837

7.  Action potential initiation in the peripheral terminals of cold-sensitive neurones innervating the guinea-pig cornea.

Authors:  Richard W Carr; Svetlana Pianova; David D McKemy; James A Brock
Journal:  J Physiol       Date:  2009-01-26       Impact factor: 5.182

8.  Conduction properties distinguish unmyelinated sympathetic efferent fibers and unmyelinated primary afferent fibers in the monkey.

Authors:  Matthias Ringkamp; Lisa M Johanek; Jasenka Borzan; Timothy V Hartke; Gang Wu; Esther M Pogatzki-Zahn; James N Campbell; Beom Shim; Raf J Schepers; Richard A Meyer
Journal:  PLoS One       Date:  2010-02-05       Impact factor: 3.240

9.  A role for polymodal C-fiber afferents in nonhistaminergic itch.

Authors:  Lisa M Johanek; Richard A Meyer; Robert M Friedman; Kenneth W Greenquist; Beom Shim; Jasenka Borzan; Tim Hartke; Robert H LaMotte; Matthias Ringkamp
Journal:  J Neurosci       Date:  2008-07-23       Impact factor: 6.167

Review 10.  Studying human nociceptors: from fundamentals to clinic.

Authors:  Steven J Middleton; Allison M Barry; Maddalena Comini; Yan Li; Pradipta R Ray; Stephanie Shiers; Andreas C Themistocleous; Megan L Uhelski; Xun Yang; Patrick M Dougherty; Theodore J Price; David L Bennett
Journal:  Brain       Date:  2021-06-22       Impact factor: 15.255

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