Literature DB >> 5501269

Presynaptic and post-synaptic inhibition elicited in the cat's dorsal column nuclei by mechanical stimulation of skin.

P Andersen, B Etholm, G Gordon.   

Abstract

1. Primary afferent depolarization (PAD), with a time course comparable with that of the PAD following limb nerve stimulation, was produced in the cuneate nucleus by mechanical stimulation of the skin of the ipsilateral forepaw. Brushing or blowing on hairs was as effective as any other form of stimulation and there was a rapid adaptation to a sustained stimulus. Up to 55% increase in excitability was produced by blowing on hairs.2. The P-wave and the PAD produced by mechanical stimulation were at a minimum in the rostral part of the cuneate nucleus and at a maximum 2-6 mm caudal to the obex.3. The distribution of the PAD produced in the gracile nucleus by blowing on the skin of the hind foot was studied by a technique allowing measurement of excitability changes near the terminals of single fibres. Minimal values were obtained rostral to the obex and maximal values 1-4 mm caudal to the obex, a distribution matching that previously determined for single cells subject to surround inhibition.4. Post-synaptic inhibition was produced in the cuneate nucleus by gentle blowing on the ipsilateral forepaw. Up to 20% fall in excitability occurred in populations of cells tested by direct electrical stimulation. IPSPs lasting up to 160 msec were observed in single cells following light mechanical stimulation in the immediate neighbourhood of these cells' receptive fields. Blocking of antidromic invasion of single cells was occasionally produced by mechanical skin stimulation.5. It is concluded that both pre- and post-synaptic inhibition must be concerned in the phenomenon of afferent surround inhibition, though there was no evidence to indicate their relative roles, qualitatively or quantitatively.6. It is shown that up to 20% reduction in transmission through the gracile or cuneate nucleus could be produced by blowing on the ipsilateral hind paw or forepaw respectively, measured as reduction in the area of the monophasically recorded lemniscal response. A single electrical stimulus to the skin of the contralateral forepaw reduced transmission through the cuneate nucleus by less than 5%.

Mesh:

Year:  1970        PMID: 5501269      PMCID: PMC1395567          DOI: 10.1113/jphysiol.1970.sp009219

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


  17 in total

1.  THE DISTRIBUTION OF THE CORTICAL FIBRES WITHIN THE NUCLEI CUNEATUS AND GRACILIS IN THE CAT.

Authors:  H G KUYPERS; J D TUERK
Journal:  J Anat       Date:  1964-04       Impact factor: 2.610

2.  MECHANISMS OF SYNAPTIC TRANSMISSION IN THE CUNEATE NUCLEUS.

Authors:  P ANDERSEN; J C ECCLES; T OSHIMA; R F SCHMIDT
Journal:  J Neurophysiol       Date:  1964-11       Impact factor: 2.714

3.  PRESYNAPTIC COMPONENT IN THE AFFERENT INHIBITION OBSERVED WITHIN TRIGEMINAL BRAIN-STEM NUCLEI OF THE CAT.

Authors:  I DARIAN-SMITH
Journal:  J Neurophysiol       Date:  1965-07       Impact factor: 2.714

4.  Functional organization in nucleus gracilis of the cat.

Authors:  G GORDON; C H PAINE
Journal:  J Physiol       Date:  1960-09       Impact factor: 5.182

5.  Excitability changes in afferent fibre terminations and their relation to slow potentials.

Authors:  P D WALL
Journal:  J Physiol       Date:  1958-06-18       Impact factor: 5.182

6.  Depolarization of central terminals of Group I afferent fibres from muscle.

Authors:  J C Eccles; F Magni; W D Willis
Journal:  J Physiol       Date:  1962-01       Impact factor: 5.182

7.  The source and mechanisms of inhibition in the lateral cervical nucleus of the cat.

Authors:  L Fedina; G Gordon; A Lundberg
Journal:  Brain Res       Date:  1968-12       Impact factor: 3.252

8.  Presynaptic inhibition of cuneate transmission by widespread cutaneous inputs.

Authors:  S J Jabbur; N R Banna
Journal:  Brain Res       Date:  1968-08-26       Impact factor: 3.252

9.  Presynaptic depolarization of dorsal column fibres by adequate stimulation.

Authors:  P Andersen; B Etholm; G Gordon
Journal:  J Physiol       Date:  1968-02       Impact factor: 5.182

10.  Excitability measurements at the central terminals of single mechano-receptor afferents during slow potential changes.

Authors:  R F Schmidt; J Senges; M Zimmermann
Journal:  Exp Brain Res       Date:  1967       Impact factor: 1.972

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  25 in total

1.  Transmission security for single kinesthetic afferent fibers of joint origin and their target cuneate neurons in the cat.

Authors:  Gordon T Coleman; Hong-Qi Zhang; Mark J Rowe
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

2.  Pharmacological aspects of neuromuscular transmission in the isolated diaphragm of the dystrophic (Rej 129) mouse.

Authors:  J B Harris; R R Ribchester
Journal:  Br J Pharmacol       Date:  1979-03       Impact factor: 8.739

3.  An electron microscopic and morphometric study on the GABA-immunoreactive terminals in the cuneate nucleus of the rat.

Authors:  C Y Wen; K N Chen; J H Lue; S A Chan; J Y Shieh
Journal:  J Anat       Date:  1992-12       Impact factor: 2.610

4.  Locomotion-related variations in excitability of spino-olivocerebellar paths to cat cerebellar cortical c2 zone.

Authors:  R Apps; M Lidierth; D M Armstrong
Journal:  J Physiol       Date:  1990-05       Impact factor: 5.182

5.  Input-output relation of transmission through cuneate nucleus.

Authors:  K Krnjević; M E Morris
Journal:  J Physiol       Date:  1976-06       Impact factor: 5.182

6.  Morphometric study of glycine-immunoreactive neurons and terminals in the rat cuneate nucleus.

Authors:  J H Lue; W F Shieh; S H Chen; J Y Shieh; C Y Wen
Journal:  J Anat       Date:  1997-10       Impact factor: 2.610

7.  Inhibition of cuneate neurones: its afferent source and influence on dynamically sensitive "tactile" neurones.

Authors:  E Bystrzycka; B S NAil; M Rowe
Journal:  J Physiol       Date:  1977-06       Impact factor: 5.182

8.  The negative potential wave evoked in cuneate nucleus by stimulation of afferent pathways: its origins and susceptibility to inhibition.

Authors:  F Andres-Trelles; C M Cowan; M A Simmonds
Journal:  J Physiol       Date:  1976-06       Impact factor: 5.182

9.  Interference of vibrations with input transmission in dorsal horn and cuneate nucleus in man: a study of somatosensory evoked potentials (SEPs) to electrical stimulation of median nerve and fingers.

Authors:  V Ibañez; M P Deiber; F Mauguière
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

10.  Human tactile detection thresholds: modification by inputs from specific tactile receptor classes.

Authors:  D G Ferrington; B S Nail; M Rowe
Journal:  J Physiol       Date:  1977-11       Impact factor: 5.182

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