Literature DB >> 7310728

Patterns of activity evoked in cerebellar interpositus nuclear neurones by natural somatosensory stimuli in awake cats.

F W Cody, R B Moore, H C Richardson.   

Abstract

1. Stable extracellular unitary recordings were made from 138 cerebellar interpositus nuclear neurones (IPNs) in awake cats. Mean background discharge, in animals in a state of relaxed wakefulness and in the absence of overt movement, was 41.0+/-2.6 impulses/sec (mean+/-s.e.m).2. Animals were trained to accept a variety of sensory testing procedures without producing detectable motor reactions. Mechanical taps (1 mm amplitude; 20 msec overall duration) applied to the main pads or dorsal surfaces of the forepaws and/or hind paws modified discharge in forty-eight of 110 IPNs tested. Response patterns to taps generally comprised one or more of three basic components, namely: short-latency excitation, e(1), at onset latencies of 13.0+/-0.9 msec (mean+/-s.e.m.) for ipsilateral forepaw (iF) and 17.0+/-0.7 msec for ipsilateral hind paw (iH); a period of reduced discharge, at latencies 25.6+/-2.6 msec for iF and 32.3+/-2.1 msec for iH; a delayed acceleration of discharge, e(2), at latencies 47.4+/-4.6 msec for iF and 46.4+/-4.1 msec for iH. The component e(1) was the most common (present in 80% of responses) and e(2) the least common (present in 18% of responses).3. The majority (> 70%) of responses of IPNs to tap stimulation of the paws comprised net excitation.4. Convergence of tap-evoked sensory input from iF and iH on to individual IPNs was evident in eight of the thirty-five units tested with stimulation of both afferent sites.5. Approximately one third of IPNs so tested were sensitive to passive manipulation of limb joints in the quiet, awake cat. Sixteen of the forty-three IPNs so tested responded to displacement of the ipsilateral wrist and/or elbow joints and three of ten IPNs so tested responded to movement of contralateral forepaw joints. Corresponding proportions of IPNs responding to passive ankle and/or knee joint displacements were sixteen of thirty-six units tested and three of three units tested for ipsilateral and contralateral hind paws respectively. Convergence of input generated by manipulation of iF and iH joints on to individual IPNs was apparent in only three of twenty-four units tested at each site.6. Tactile stimulation (brushing fur, gentle pressure on the skin) of iF influenced discharge in twelve of thirty-seven IPNs tested and comparable iH-related cutaneous sensory fields were found for fourteen of twenty-eight IPNs tested.7. The modulations of discharge of IPNs associated with active movements of the stimulated limb were usually far more pronounced than those elicited by somatosensory stimulation in the quiet, relaxed animal.8. Responses of IPNs to natural somatosensory stimulation in the awake cat are compared with those previously described for anaesthetized or decerebrate preparations and with those found for electrical stimulation of cutaneous nerves in awake cats. In general IPN response patterns to precisely timed tap stimulation of the paws in the awake animal closely resembled those that would have been predicted from the earlier studies, although the time course of responses differed in certain respects.

Entities:  

Mesh:

Year:  1981        PMID: 7310728      PMCID: PMC1246774          DOI: 10.1113/jphysiol.1981.sp013810

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


  23 in total

1.  Effects of afferent volleys from the limbs on the discharge patterns of interpositus neurones in cats anaesthetized with alpha-chloralose.

Authors:  D M Armstrong; B Cogdell; R Harvey
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

2.  Cerebellar responses to teleceptive stimuli in alert monkeys.

Authors:  J A Mortimer
Journal:  Brain Res       Date:  1975-01-17       Impact factor: 3.252

Review 3.  Cerebrocerebellar communication systems.

Authors:  G I Allen; N Tsukahara
Journal:  Physiol Rev       Date:  1974-10       Impact factor: 37.312

4.  Synaptic excitation of red nucleus neurones by fibres from interpositus nucleus.

Authors:  K Toyama; N Tsukahara; K Kosaka; K Matsunami
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

5.  Patterns of convergence onto interpositus neurons from peripheral afferents.

Authors:  J C Eccles; I Rosén; P Scheid; H Táboríková
Journal:  J Neurophysiol       Date:  1974-11       Impact factor: 2.714

6.  Temporal patterns of responses of interpositus neurons to peripheral afferent stimulation.

Authors:  J C Eccles; I Rosén; P Scheid; H Táboríková
Journal:  J Neurophysiol       Date:  1974-11       Impact factor: 2.714

7.  Cutaneous mechanoreceptors influencing impulse discharges in cerebellar cortex. 3. In Purkynĕ cells by climbing fiber input.

Authors:  J C Eccles; N H Sabah; R F Schmidt; H Táboríková
Journal:  Exp Brain Res       Date:  1972-10-29       Impact factor: 1.972

8.  Glass-coated platinum-plated tungsten microelectrodes.

Authors:  E G Merrill; A Ainsworth
Journal:  Med Biol Eng       Date:  1972-09

9.  Discharge of Purkinje and cerebellar nuclear neurons during rapidly alternating arm movements in the monkey.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1968-09       Impact factor: 2.714

10.  Comparison of response of cerebellar Purkinje cells and interpositus neurones in chloralose-anaesthetized cats.

Authors:  J M Alexander; T A Asghar; M N Chetty; F W Cody; H C Richardson
Journal:  J Physiol       Date:  1980-01       Impact factor: 5.182

View more
  17 in total

1.  Sensory characteristics of monkey thalamic and motor cortex neurones.

Authors:  E G Butler; M K Horne; J A Rawson
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

2.  Activity of deep cerebellar nuclear cells during classical conditioning of nictitating membrane extension in rabbits.

Authors:  N E Berthier; J W Moore
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

3.  Control of voluntary and optogenetically perturbed locomotion by spike rate and timing of neurons of the mouse cerebellar nuclei.

Authors:  Rashmi Sarnaik; Indira M Raman
Journal:  Elife       Date:  2018-04-16       Impact factor: 8.140

Review 4.  Processing of limb kinematics in the interpositus nucleus.

Authors:  Antonino Casabona; Gianfranco Bosco; Vincenzo Perciavalle; Maria Stella Valle
Journal:  Cerebellum       Date:  2010-03       Impact factor: 3.847

Review 5.  Consensus paper: current views on the role of cerebellar interpositus nucleus in movement control and emotion.

Authors:  Vincenzo Perciavalle; Richard Apps; Vlastislav Bracha; José M Delgado-García; Alan R Gibson; Maria Leggio; Andrew J Carrel; Nadia Cerminara; Marinella Coco; Agnès Gruart; Raudel Sánchez-Campusano
Journal:  Cerebellum       Date:  2013-10       Impact factor: 3.847

6.  Cerebellar unit responses of the mossy fibre system to passive movements in the decerebrate cat. I. Responses to static parameters.

Authors:  F P Kolb; F J Rubia; E Bauswein
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

Review 7.  Eccentric activation and muscle damage: biomechanical and physiological considerations during downhill running.

Authors:  R G Eston; J Mickleborough; V Baltzopoulos
Journal:  Br J Sports Med       Date:  1995-06       Impact factor: 13.800

8.  Cerebellar feedback signals of a passive hand movement in the awake monkey.

Authors:  E Bauswein; F P Kolb; F J Rubia
Journal:  Pflugers Arch       Date:  1984-11       Impact factor: 3.657

9.  Discharges of nucleus interpositus neurones during locomotion in the cat.

Authors:  D M Armstrong; S A Edgley
Journal:  J Physiol       Date:  1984-06       Impact factor: 5.182

Review 10.  Synaptic inhibition, excitation, and plasticity in neurons of the cerebellar nuclei.

Authors:  Nan Zheng; Indira M Raman
Journal:  Cerebellum       Date:  2010-03       Impact factor: 3.847

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.