Literature DB >> 2073951

Functional organization of the nociceptive withdrawal reflexes. I. Activation of hindlimb muscles in the rat.

J Schouenborg1, J Kalliomäki.   

Abstract

1. The organization of the nociceptive hindlimb withdrawal reflexes was investigated in 93 halothane/nitrous oxide anesthetized rats. Electromyographical techniques were used to record reflex activity in single motor units. 2. Most of the hindlimb muscles were activated by noxious mechanical stimulation of the skin of the ipsilateral hindlimb. These were the plantar flexors of the digits, the pronators of the paw, the dorsiflexors and the plantar flexors of the ankle, the flexors of the knee, the flexors of the hip and the adductors. By grading the stimulus intensity it was shown that all these muscles received input from cutaneous nociceptors. 3. Noxious stimulation of the skin failed to activate the obturator, knee extensors and m. tibialis posterior and, in most rats tested, m. semimembranosus and m. adductor magnus. The plantar flexors of the ankle, while exhibiting a clear nocireceptive field in all rats tested, had a high threshold and responded much more weakly than the dorsiflexors of the ankle. Thus, responses in muscles which oppose gravity in the standing position were either very weak or absent. 4. The present study shows that each of the activated hindlimb muscles has a highly organized nocireceptive field on the skin, which is related to the withdrawal movement caused by the muscle itself. Each of the muscles normally causes the withdrawal of its receptive field when the foot is on the ground. The skin area most effectively withdrawn, in this situation, corresponds to the most sensitive area of the nocireceptive field. However, with the exception of the plantar flexors of the digits and/or the ankle, each of the hindlimb muscles also withdraws the major parts of their receptive fields when the foot is off the ground. The locations of the nocireceptive fields were independent of the position of the hindlimb. These characteristics of the nociceptive withdrawal reflexes are the basis for their "local sign" (Sherrington 1906). 5. The threshold and the time course of reflex activation were different in different muscles. However, muscles with a similar action; the plantar flexors of the digits, the pronators of the paw, the dorsiflexors of the digits, the flexors of the knee and the adductors, respectively, had similar thresholds and time courses. Furthermore, the threshold and latency of activation of each muscle increased towards the border of its nocireceptive field, reflecting a decreasing sensitivity. These findings explain the progressive recruitment of muscles during increasing strength of noxious stimulation, termed "irradiation" (Sherrington 1906).(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2073951     DOI: 10.1007/BF00232194

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  34 in total

1.  The rule of reflex response in the limb reflexes of the mammal and its exceptions.

Authors:  T G Brown; C S Sherrington
Journal:  J Physiol       Date:  1912-05-06       Impact factor: 5.182

2.  Bilateral facilitatory and inhibitory skin areas of spinal motoneurones of cat.

Authors:  D MEGIRIAN
Journal:  J Neurophysiol       Date:  1962-01       Impact factor: 2.714

3.  Excitatory and inhibitory skin areas for flexor and extensor motoneurons.

Authors:  K E HAGBARTH
Journal:  Acta Physiol Scand Suppl       Date:  1952

4.  A critical analysis of the experimental evaluation of nociceptive reactions in animals.

Authors:  K Ramabadran; M Bansinath
Journal:  Pharm Res       Date:  1986-10       Impact factor: 4.200

5.  Dynamic receptive field plasticity in rat spinal cord dorsal horn following C-primary afferent input.

Authors:  A J Cook; C J Woolf; P D Wall; S B McMahon
Journal:  Nature       Date:  1987 Jan 8-14       Impact factor: 49.962

6.  Primary afferent units from the hairy skin of the rat hind limb.

Authors:  B Lynn; S E Carpenter
Journal:  Brain Res       Date:  1982-04-22       Impact factor: 3.252

7.  Reflex pathways from group II muscle afferents. 1. Distribution and linkage of reflex actions to alpha-motoneurones.

Authors:  A Lundberg; K Malmgren; E D Schomburg
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

8.  Unmyelinated nociceptive units in two skin areas of the rat.

Authors:  E Fleischer; H O Handwerker; S Joukhadar
Journal:  Brain Res       Date:  1983-05-09       Impact factor: 3.252

9.  The effects of decerebration and destruction of nucleus raphe magnus, periaqueductal grey matter and brainstem lateral reticular formation on the depression due to surgical trauma of the jaw-opening reflex evoked by tooth-pulp stimulation in the cat.

Authors:  R W Clarke
Journal:  Brain Res       Date:  1985-04-22       Impact factor: 3.252

10.  Cutaneous receptive field and morphological properties of hamstring flexor alpha-motoneurones in the rat.

Authors:  A J Cook; C J Woolf
Journal:  J Physiol       Date:  1985-07       Impact factor: 5.182

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  48 in total

1.  Common principles of sensory encoding in spinal reflex modules and cerebellar climbing fibres.

Authors:  Martin Garwicz; Anders Levinsson; Jens Schouenborg
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

Review 2.  State-dependent modulation of sensory feedback.

Authors:  H Hultborn
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

3.  Spinal sensorimotor transformation: relation between cutaneous somatotopy and a reflex network.

Authors:  Anders Levinsson; Hans Holmberg; Jonas Broman; Mengliang Zhang; Jens Schouenborg
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

4.  Changes in correlation between spontaneous activity of dorsal horn neurones lead to differential recruitment of inhibitory pathways in the cat spinal cord.

Authors:  D Chávez; E Rodríguez; I Jiménez; P Rudomin
Journal:  J Physiol       Date:  2012-01-23       Impact factor: 5.182

5.  Test-retest reliability of the nociceptive withdrawal reflex and electrical pain thresholds after single and repeated stimulation in patients with chronic low back pain.

Authors:  José A Biurrun Manresa; Alban Y Neziri; Michele Curatolo; Lars Arendt-Nielsen; Ole K Andersen
Journal:  Eur J Appl Physiol       Date:  2010-09-03       Impact factor: 3.078

6.  Modulation of heat evoked nociceptive withdrawal reflexes by painful intramuscular conditioning stimulation.

Authors:  Ole K Andersen; Carsten Dahl Mørch; Lars Arendt-Nielsen
Journal:  Exp Brain Res       Date:  2006-09-02       Impact factor: 1.972

7.  The postsynaptic dorsal column pathway mediates cutaneous nociceptive information to cerebellar climbing fibres in the cat.

Authors:  C F Ekerot; M Garwicz; J Schouenborg
Journal:  J Physiol       Date:  1991-09       Impact factor: 5.182

8.  Topography and nociceptive receptive fields of climbing fibres projecting to the cerebellar anterior lobe in the cat.

Authors:  C F Ekerot; M Garwicz; J Schouenborg
Journal:  J Physiol       Date:  1991-09       Impact factor: 5.182

Review 9.  In search of lost presynaptic inhibition.

Authors:  Pablo Rudomin
Journal:  Exp Brain Res       Date:  2009-03-26       Impact factor: 1.972

10.  Parallel nociceptive reflex pathways with negative and positive feedback functions to foot extensors in the cat.

Authors:  E D Schomburg; H Steffens; N Wada
Journal:  J Physiol       Date:  2001-10-15       Impact factor: 5.182

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