Literature DB >> 6653701

Cerebellar output response to afferent stimulation: energy consumption and unit activity in the cat fastigial nucleus.

C Batini, J F Bernard, C Buisseret-Delmas, G Horcholle-Bossavit.   

Abstract

The cerebellar output function was studied using cerebellopetal proprioceptive stimulation which produces simple and complex excitatory discharges as well as inhibitory activity in the Purkinje cells. The activity of the intracerebellar nuclei (and of the entire brain stem) was measured by the energy consumption as revealed with the [14C )-2-deoxyglucose method. The stimulations consisted of repetitive (1-20 c/s) electrical excitation of the nerve leading to the inferior oblique, to the masseteric and to the gastrocnemius soleus muscle. Compared to a group of non-stimulated controls, heavy bilateral labeling was obtained in the posterior pole of the fastigial nucleus. This was not observed with stimulation of the vibrissal pad which, however, produced a clear increase of [14C]-2-deoxyglucose uptake in the secondary trigeminal complex. Labeling of the posterior part of the fastigial nuclei was suppressed by ablation or pharmacologic inactivation of the overlying cerebellar cortex which suppresses the inhibitory activity of the Purkinje cells into the nuclear cells. Labeling of the posterior fastigial nuclei was also decreased in animals not stimulated but with ablation or pharmacologic inactivation of the overlying cerebellar cortex. The hypothesis proposed is that the marking results are the consequence of an increased activity in the Purkinje cell terminals. The activity of the Purkinje cells was also recorded extracellulary both before and during repetitive stimulation of a muscle nerve. The discharge activity of those in the cerebellar vermis and giving axons to the posterior fastigial nucleus was increased by the stimulation, whereas the activity of those of the hemispheral parts remained unchanged. Units in the fastigial nucleus were also recorded. Their activity was found to be deeply depressed so that only a few units were encountered and no further decrease of their discharge could be detected with the stimulation of a muscle nerve. Nevertheless, using the present data and those previously obtained, the conclusion is advanced that the cerebellar output function is actually decreased during afferent cerebellar stimulation.

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Year:  1983        PMID: 6653701     DOI: 10.1007/BF00238033

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


  31 in total

1.  The [14C]deoxyglucose method for the measurement of local cerebral glucose utilization: theory, procedure, and normal values in the conscious and anesthetized albino rat.

Authors:  L Sokoloff; M Reivich; C Kennedy; M H Des Rosiers; C S Patlak; K D Pettigrew; O Sakurada; M Shinohara
Journal:  J Neurochem       Date:  1977-05       Impact factor: 5.372

2.  Actions of afferent impulses from muscle receptors on cerebellar Purkynĕ cells. I. Responses to muscle vibration.

Authors:  K Ishikawa; S Kawaguchi; M J Rowe
Journal:  Exp Brain Res       Date:  1972       Impact factor: 1.972

3.  Structural organization of the fastigial nucleus. II. Afferent fiber systems.

Authors:  M Matsushita; N Iwahori
Journal:  Brain Res       Date:  1971-02-05       Impact factor: 3.252

4.  Neuronal responses to eye muscle stretch in cerebellar lobule VI of the cat.

Authors:  D W Schwarz; R D Tomlinson
Journal:  Exp Brain Res       Date:  1977-01-18       Impact factor: 1.972

5.  The central projections of trigeminal primary afferent neurons in the cat as determined by the tranganglionic transport of horseradish peroxidase.

Authors:  C F Marfurt
Journal:  J Comp Neurol       Date:  1981-12-20       Impact factor: 3.215

6.  On the origin of the climbing fibers of the cerebellum. An experimental study in the cat with an autoradiographic tracing method.

Authors:  J Courville; F Faraco-Cantin
Journal:  Neuroscience       Date:  1978       Impact factor: 3.590

7.  Distributions of vibrissae afferent fiber collaterals in the trigeminal nuclei as revealed by intra-axonal injection of horseradish peroxidase.

Authors:  H Hayashi
Journal:  Brain Res       Date:  1980-02-10       Impact factor: 3.252

8.  Suppression of simple spike discharges of cerebellar Purkinje cells by impulses in climbing fibre afferents.

Authors:  J A Rawson; K Tilokskulchai
Journal:  Neurosci Lett       Date:  1981-09-01       Impact factor: 3.046

9.  The olivocerebellar system. I. Delayed and slow inhibitory effects: an overlooked salient feature of cerebellar climbing fibers.

Authors:  F Colin; J Manil; J C Desclin
Journal:  Brain Res       Date:  1980-04-07       Impact factor: 3.252

10.  Intraperitoneal administration and other modifications of the 2-deoxy-D-glucose technique.

Authors:  R C Meibach; S D Glick; D A Ross; R D Cox; S Maayani
Journal:  Brain Res       Date:  1980-08-11       Impact factor: 3.252

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  2 in total

1.  Release of cerebellar inhibition by climbing fiber deafferentation.

Authors:  C Batini; J M Billard
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

2.  Harmaline induced tremor. III. A combined simple units, horseradish peroxidase, and 2-deoxyglucose study of the olivocerebellar system in the rat.

Authors:  J F Bernard; C Buisseret-Delmas; C Compoint; S Laplante
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

  2 in total

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