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J M Billard

Publications and source records attributed to J M Billard.

42 records · Page 3Linked to original sources

Cerebellar output regulation by the climbing and mossy fibers with and without the inferior olive.

The activity of the olivocerebellar complex and the structures related in series with it have been studied using the complementary action of harmaline and 3-acetylpyridine to isolate the two principal inputs to the cerebellar Purkinje cells. The activities of the various nuclei as well as the entire brain have been simultaneously monitored using the [14C]2-deoxy-glucose method under the various combined effects of the pharmacological agents. (1) Tremogenic doses of harmaline increased the frequency of discharge in selected parts of the olivocerebellar system, increasing climbing fiber input and reducing Purkinje cell simple spike discharges in corresponding parts of the cerebellar cortex. The metabolic activity increased in the inferior olive and in the red nucleus. The results are interpreted as a net reduction of Purkinje cell inhibition on their target neurons, leading to a facilitatory cerebellar output. (2) Systemic injection of neurotoxic doses of 3-acetylpyridine selectively produced total degeneration of the neurons in the inferior olive, resulting in the suppression of complex spikes and a net increase in simple spike output from the Purkinje cells. The metabolic consequences were a reduction or absence in the inferior olive, decrease in the red nucleus, and increases in the Purkinje cell target neuron regions, including the intracerebellar and vestibular nuclei. The study of long survival times following the neurotoxic treatment revealed a transient metabolic marking of the inferior olive during the active glial processes accompanying the degeneration. In other parts the radioautographic changes caused by the destruction of the inferior olive persisted for about 1 month after the administration of the drug. (3) Tremogenic doses of harmaline were given to rats at different times following treatment with 3-acetylpyridine. It was demonstrated that: (a) intoxication of the inferior olive started within the second hour after 3-acetylpyridine administration, corresponding to the time at which the metabolic response to harmaline was also abolished; and (b) the increased metabolic activity produced by harmaline in the olivocerebellar complex was a consequence of an increased activity of the neurons of the inferior olive rather than a direct pharmacological effect of the drug. (4) Partial lesions of the inferior olive led to increased metabolic activity of those parts of the intracerebellar nuclei topographically related to the destroyed parts of the inferior olive. (5) In 3-acetylpyridine-treated animals, local ablation as well as local inactivation of the cerebellar cortex produced localized suppression of the intense labeling in the intracerebellar nuclei obtained in these animals. Since these regions receive synapses which are normally inhibitory, suppression of labeling clearly supports the hypothesis that regional marking may very well be produced by the activity of the presynaptic terminals themselves...

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[Cerebellar disfacilitation after pharmacological destruction of the inferior olive].

The total selective destruction of the inferior olive by 3-acetylpyridine produces a marked increase in the metabolic activity at the intracerebellar nuclei. This increase is locally suppressed by partial ablation or local inactivation of the corresponding regions in the cerebellar cortex, suggesting its localization in the intranuclear presynaptic terminals of the Purkinje cells. In a second series of experiments, it is demonstrated that Purkinje cells of the cerebellar cortex deprived of their climbing fibers and therefore of their complex spikes by destruction of the inferior olive, increase their firing frequency of simple spikes. As a consequence, there is a decreased frequency of discharge of their target neurones in the intracerebellar nuclei; the net result of suppression of the inferior olive is thus an increased cortico-nuclear inhibitory effect.

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Topographic organization of the interpositorubral connections in the rat. A WGA-HRP study.

The projections from the anterior (NIA) and posterior (NIP) interposed nuclei to the magnocellular red nucleus (RNm) have been investigated in the rat, using the retrograde transport of horseradish peroxidase-wheatgerm agglutinin conjugate. Projections from the NIA extend throughout the RNm, whereas those from the NIP only reach its medial aspect. In addition, a topographical organization of the NIA-RNm pathway was found, such that the medial NIA projects ventrally, the lateral NIA projects dorsally.

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The red nucleus activity in rats deprived of the inferior olivary complex.

The long-term effects of the inferior olive destruction on the red nucleus activity, were studied in the rat following injection of 3-acetylpyridine. As soon as the olivary activity was suppressed, the discharge of the rubral units drastically decreased. Then, they progressively recovered the control frequency during the first month, although a normal rubral activity was not restored up to 8 months. The hypothesis is advanced that the olivocerebellar system is essential to shape the activity of the rubrospinal pathway.

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NMDA receptor activation in the aged rat: electrophysiological investigations in the CA1 area of the hippocampal slice ex vivo.

The effects of aging on activation of N-methyl-D-aspartate (NMDA) receptors were studied in the CA1 field of hippocampal slices from young (2-4 months old) and aged (25-32 months old) Sprague-Dawley rats with the use of ex vivo extra- and intracellular electrophysiological recording techniques. No significant age-related changes of the unitary NMDA-receptor mediated excitatory postsynaptic potentials (EPSPs), recorded from the pyramidal cells after stimulation of the stratum radiatum in a magnesium-free medium and isolated in the presence of the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione, were found. Simultaneously, the magnitude of synaptic plasticity which involved NMDA receptor activation was not altered. No significant age-related modifications in the mechanisms controlling glutamate release and of postsynaptic NMDA receptor responsiveness were revealed. Considering the 30-40% decrease in NMDA binding sites in the aged hippocampus, our results suggest the occurrence of compensatory mechanisms which are discussed.

Aging↗

Immunolesion of the cholinergic basal forebrain: effects on functional properties of hippocampal and septal neurons.

Deficits in cholinergic function have been documented in a variety of brain disorders including Alzheimer's Disease and, to a lesser extent, in normal ageing. In the present article, we have reviewed our recent findings on the effects of the loss of basal forebrain cholinergic neurons on the functional properties of the septohippocampal pathway. In vivo and ex vivo investigations were performed in rats following basal forebrain cholinergic lesion with the specific immunotoxin 192 IgG-saporin. Our results suggest a significant contribution of cholinergic neurons in the rhythmically bursting activity recorded within the medial septum. In addition, they give evidence that acetylcholine may tonically decrease the glutamatergic synaptic responses in the hippocampus whereas the GABAergic mediated inhibitory potentials are not affected. The possible contribution of these cholinergic mechanisms in the age-related functional alterations of the septohippocampal activity is discussed.

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