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Y Lamour

Publications and source records attributed to Y Lamour.

At least 91 records · Page 5Linked to original sources

Modifications in the cortical regional distribution of choline acetyltransferase, somatostatin and somatostatin binding sites in the normal rat and following lesion of the nucleus basalis.

The regional distribution of choline acetyltransferase activity, somatostatin levels and 125I-CGP 23996 (a somatostatin agonist analog) specific binding sites in 10 separate zones of the cerebral cortex was analyzed. The study was performed in normal rats as well as 15 days after unilateral excitotoxic lesion of the nucleus basalis. A significant correlation was found in the controls between the regional distribution of choline acetyltransferase activity and somatostatin concentrations, both most highly concentrated in the piriform and entorhinal cortex. In contrast, the regional density of 125I-CGP 23996 binding sites correlated neither with choline acetyltransferase activity nor with somatostatin levels. Unilateral lesions of the basal forebrain decreased choline acetyltransferase activity in the frontal and parietal cortex, while 125I-CGP 23996 binding decreased in frontal and occipital regions. No decrease in somatostatin content was observed. The results suggest that, in rats, cortical somatostatin receptors could be associated with cholinergic afferents from the nucleus basalis in the frontal cortex only.

Animals↗

Septo-hippocampal neurons in the rat: further study of their physiological and pharmacological properties.

Medial septal-nucleus of the diagonal band of Broca area (MS-nDBB) neurons, identified by their antidromic response to the electrical stimulation of the fimbria and/or hippocampus, were studied in the rat under various conditions of anesthesia. These septo-hippocampal neurons (SHNs) were classified into 4 groups on the basis of: (i) their antidromic latency; and (ii) the presence or absence of a rhythmically bursting pattern of spontaneous discharge. The rhythmically bursting activity (43.5% of the SHNs) was highly dependent on the anesthetic conditions. The groups of SHNs differed in their mean conduction velocity and rate of spontaneous activity. In contrast, irrespective of their classification in a particular group, the large majority of the SHNs could be excited by the iontophoretic application of cholinergic agonists. Beside the SHNs, two other populations of MS-nDBB neurons could be identified by electrical antidromic stimulation: neurons projecting to the amygdala (Am) and neurons projecting through the medial forebrain bundle (MFB). Half of the MS-nDBB neurons projecting to Am were also antidromically driven from the fimbria. The axonal branch projecting to Am had a slower conduction velocity than that projecting to hippocampus. In contrast MS-nDBB neurons projecting through the MFB were never antidromically driven from the fimbria, although they received orthodromic inputs. They had a slower conduction velocity than the other groups of MS-nDBB neurons.

Amygdala↗

Comparison of septo-hippocampal with basalo-cortical projection neurons in the rat: an electrophysiological approach.

The electrophysiological properties of septo-hippocampal (SHNs) and basalo-cortical neurons (BCNs) identified by antidromic stimulation were compared in rats anesthetized with urethane. SHNs and BCNs had comparable conduction velocities (about 2-3 m/s) and relatively high spontaneous firing rates (about 20 impulses/s). In contrast, they differed in their pattern of spontaneous discharge as studied by generating inter-spike interval histograms. Many BCNs had a regular pattern of discharge. Among SHNs, about 40% had a spontaneous rhythmically bursting pattern of discharge, whereas the remaining 60% had a more or less irregular pattern. These results suggest that SHNs represent a more heterogeneous neuronal population than BCNs, and that central cholinergic neurons involved in different systems might also have different properties.

Action Potentials↗

Basal forebrain neurons projecting to the rat frontoparietal cortex: electrophysiological and pharmacological properties.

Neurons located in the ventromedial globus pallidus (nucleus basalis) and substantia innominata, that were antidromically driven by electrical stimulation of the frontoparietal cortex, were recorded in the urethane anesthetized rat. The basalocortical neurons (BCNs) were antidromically driven with latencies of 1.1-13.5 ms, giving conduction velocities of 0.6-6.8 m/s. Many BCNs had regular patterns of spontaneous discharge (mean spontaneous activity: 20 impulses/s). Most BCNs were not responsive to non-noxious peripheral somatic stimulation. BCNs were readily excited by the iontophoretic application of glutamate and strongly inhibited by GABA. Eighty-five percent of the BCNs could be excited by acetylcholine. They could also be excited by cholinergic agonists. Muscarinic agonists excited a higher proportion of BCNs than nicotinic agonists. Excitatory responses to acetylcholine, carbachol and muscarinic agonists were abolished by atropine.

Acetylcholine↗

Septohippocampal neurons after intraventricular AF64A administration in rats: an electrophysiological study.

The putative cholinergic neurotoxin, ethylcholine aziridinium ion (AF64A), was injected bilaterally into the cerebral ventricles of male rats. The properties of the medial septum-nucleus of the diagonal band of Broca's area (MS-nDBB) neurons were studied 4 to 6 or 19 to 23 days following injections. The spontaneous activity of those neurons was higher in the injected animals, but their responses to glutamate and cholinergic agonists were not modified. The proportion of orthodromic responses elicited by fimbria-fornix stimulation in MS-nDBB neurons was unchanged. In contrast, the proportion of septohippocampal neurons (SHNs) identified by the antidromic stimulation of the fimbria-fornix was smaller in pretreated animals and their mean antidromic latency was shorter. These results suggest that intracerebroventricular administration of the neurotoxin AF64A is followed by changes in the properties of MS-nDBB neurons and specifically by the disappearance of a subpopulation of SHNs.

Animals↗

[Excitability of septo-hippocampal axon terminals: changes as a function of the level of neuronal activity].

The septo-hippocampal terminals were electrically stimulated at the level of the gyrus dentatus in urethane anesthetized rats and antidromic responses were recorded in the medial septum. The excitability of the terminals was assessed by the threshold of terminal antidromic activation. An increase in the discharge frequency of the septal neurons following a microiontophoretic application of glutamate to their soma induced an increase in the antidromic activation threshold, i.e. a decrease in excitability of the terminals. An application of GABA which inhibited septal neuronal activity, induced a decrease in the antidromic activation threshold, i.e. an increase in the terminal excitability of septo-hippocampal neurons. These results are discussed in the light of the presynaptic autoreceptor hypothesis.

Acetylcholine↗

Rearrangement of chromosome 21 in Alzheimer's disease.

We have analyzed the DNA from four patients suffering from a dementia of the Alzheimer type and of four controls of identical age. Estimates of the copy numbers of two genes located on chromosome 21, SOD1 and ETS2, gave the following results: in all the cases there was duplication of ETS2 whereas SOD1 was normal. These preliminary results indicate that the segment of chromosome 21(q21----q22.1) is rearranged in all the four patients who were investigated.

Alzheimer Disease↗

Septohippocampal neurons in the rat: an in vivo intracellular study.

In vivo intracellular recordings were obtained from septohippocampal neurons identified by their antidromic response to electrical stimulation of the fimbria in rats anesthetized with pentobarbital or urethane. Beside the antidromic response, fimbria stimulation evoked a short-latency depolarizing potential (EPSP) followed by an hyperpolarizing potential which reversed polarity when recorded with KCl-filled electrodes. This IPSP is therefore likely to be chloride-dependent. It was followed by a long-lasting (80-250 ms) depolarizing potential often associated with a burst of spikes. Septohippocampal neurons therefore receive an inhibitory, chloride-mediated, input which itself triggers a long-lasting excitatory event. These results are consistent with extracellular observations. Their significance in the septohippocampal circuitry is discussed.

Animals↗

Effects of TRH, cyclo-(His-Pro) and (3-Me-His2)TRH on identified septohippocampal neurons in the rat.

Neurons located in the medial septum-nucleus of the diagonal band of Broca (vertical limb) and antidromically activated by electrical stimulation of the fimbria were recorded in urethane anesthetized rats. Forty-three percent of these septohippocampal neurons (SHNs) were excited by the iontophoretic application of thyrotropin-releasing hormone (TRH). Rhythmically bursting SHNs were more often excited (63%) by TRH than the non-bursting SHNs (35%). The majority of the TRH-sensitive SHNs could also be excited by cholinergic agonists. TRH-induced excitations were not abolished by the simultaneous application of atropine. Potentiation by TRH of acetylcholine, carbachol or glutamate-induced excitations of SHNs were rarely observed. Cyclo (His-Pro) and (3-Me-His2)-TRH were observed to have similar, although less dramatic, effects. These results demonstrate that the SHNs, which are the neurons of origin of the septohippocampal pathway, are readily excited by TRH.

Acetylcholine↗

Activation of identified septo-hippocampal neurons by noxious peripheral stimulation.

Septo-hippocampal neurons (SHNs) were recorded from the medial septum-diagonal band area of rats anaesthetized with either urethane or fluothane. They were identified by their antidromic response to the electrical stimulation of the fimbria. Their responses to peripheral somatic noxious and non-noxious stimulation were studied. Non-noxious natural stimulations were relatively ineffective. In contrast, 68% of the SHNs were driven by noxious stimulation. The SHNs could be driven either by mechanical or thermal stimulation. Intraperitoneal injection of bradykinin excited about half of the SHNs. Some neurons were able to encode stimulus intensity (strength of the mechanical stimulation and/or temperature of the thermal stimulation). The receptive fields of the SHNs were large, usually involving half of the body or the whole body surface. These results suggest that SHNs, which are at the origin of the cholinergic septo-hippocampal pathway, might be involved in cerebral mechanisms related to nociception.

Animals↗

Cerebral neocortical neurons in the aged rat: spontaneous activity, properties of pyramidal tract neurons and effect of acetylcholine and cholinergic drugs.

The properties of cortical cerebral neurons have been studied and compared in 2, 22 and 26 month-old Sprague-Dawley rats, using electrophysiological techniques. The mean spontaneous activity of the neurons in old animals (unidentified as well as pyramidal tract neurons) was not different from that of young adult rats. In contrast the mean latency of the antidromic response of pyramidal tract neurons to pyramidal tract stimulation was significantly longer in 26 month-old animals. No difference was observed in the effects of the excitatory amino acid glutamate applied by iontophoresis. The percentage of cortical neurons excited by the iontophoretic application of acetylcholine was similar in young and old animals. Neither the laminar distribution, nor the individual sensitivity of these neurons to acetylcholine were found to be modified. The pharmacological properties of the acetylcholine-induced excitations were unchanged, exhibiting muscarinic as well as nicotinic properties. These results are consistent with the suggestion that the impairment of the cholinergic system with aging is for a large part presynaptic. They also emphasize the fact that several physiological and pharmacological properties of the cerebral cortical neurons show little change with age in Sprague-Dawley rats.

Acetylcholine↗

Bethanechol decreases reaction time in senile dementia of the Alzheimer type.

Bethanechol, a muscarinic cholinergic agonist, was injected subcutaneously in eight cases of senile dementia of the Alzheimer type. Simple reaction time was measured before, 15 min and 30 min following the injection. Before injection, the patients had significantly longer reaction time than non-demented controls. A significant shortening of the reaction time was observed 15 min but not 30 min after injection. A second group of eight patients with senile dementia of the Alzheimer type, matched for age and mental impairment were injected with saline. No significant shortening of the reaction time was observed. These results suggest that the reaction time can be shortened by a muscarinic agonist in dementia of the Alzheimer type.

Adult↗

[Properties of thalamocortical cells identified by antidromic stimulation in the ventrolateral and ventrobasal thalamic nuclei in rats].

The physiological and pharmacological properties of thalamocortical neurons, identified by electrical antidromic stimulation of the frontoparietal cortex, were studied in the ventrobasal and ventrolateral thalamic nuclei in urethane anaesthetized rats. The spontaneous activity and conduction velocity of these neurons were similar in both nuclei. At both sites, thalamocortical neurons could be excited through iontophoretic application of acetylcholine and muscarinic or nicotinic agonists. Despite the known differences in thalamic organization of the two species, these properties are quite similar to those described in cat by other authors.

Acetylcholine↗

Septo-hippocampal and other medial septum-diagonal band neurons: electrophysiological and pharmacological properties.

Neurons located in the medial septum-nucleus of the diagonal band (vertical limb) area and antidromically activated by electrical stimulation of the fimbria were recorded in urethane anesthetized rats. Forty-five percent of these septo-hippocampal neurons (SHNs) discharged rhythmically in short bursts (mean burst frequency, 4 Hz). They were antidromically driven at short latencies from the fimbria. SHNs driven at long latencies (above 5 ms) were never bursting neurons. Fimbria stimulation also had a powerful inhibitory effect on the spontaneous activity of SHNs. The vast majority of the septo-hippocampal neurons were excited by the iontophoretic application of acetylcholine or cholinergic agonists, carbachol being the most effective. The acetylcholine-induced excitations were readily abolished by atropine. In contrast hexamethonium and mecamylamine were less effective. The rhythmic bursting activity could not be consistently altered by the iontophoretic application of cholinergic agonists or antagonists or of divalent cations. SHNs were also sensitive to various other putative neurotransmitters (substance P, GABA) known to play a role in the medial septal area. Bursting neurons and ACh-sensitive neurons were less frequent among unidentified medial septal neurons. The regulation of the septo-hippocampal cholinergic pathway is therefore not likely to be due to a direct feedback inhibition by locally released acetylcholine. However a strong inhibitory feedback could be exerted by the hippocampo-septal pathway impinging directly or indirectly on septo-hippocampal neurons.

Animals↗

In vivo electrochemical detection of 5-hydroxyindoles in rat cerebral cortex and spinal cord: differential effects of p-chloroamphetamine, probenecid and clorgyline.

Differential pulse voltammetry associated with carbon fiber microelectrodes was used to detect the 300 mV signal which is known to reflect the concentration of 5-hydroxyindoles in the spinal cord and cerebral neocortex of rats anesthetized with urethane or chloral hydrate. The intraperitoneal injection of p-chloroamphetamine resulted in an increase in the amplitude of the signal in the neocortex but not in the spinal cord. Administration of clorgyline did not consistently modify the signal monitored in the neocortex whereas it decreased in the spinal cord. Probenecid induced a larger increase in 5-hydroxyindoles in the neocortex than in the spinal cord. These results demonstrate that different parts of the serotonergic system might be differentially sensitive to drugs affecting serotonin metabolism.

Amphetamines↗

Cortical projections of the nucleus of the diagonal band of Broca and of the substantia innominata in the rat: an anatomical study using the anterograde transport of a conjugate of wheat germ agglutinin and horseradish peroxidase.

The projections of the nucleus of the diagonal band of Broca and of the substantia innominata to the cerebral cortex were studied in the rat, using the anterograde transport of wheat germ agglutinin conjugated with horseradish peroxidase. Following diagonal band injections, fibers were observed ascending in the septum and reaching the cingulate cortex. They had a rostrocaudal, horizontal direction, mostly in layer VI and could be followed over long distances on sagittal sections. The fibers gave off collaterals which were seen ascending in the cerebral cortex and reaching more superficial layers. Following substantia innominata injections, fibers were observed to take two routes: the first one identical to the one described above and a second through the caudate-putamen reaching the temporo-insular cortex. Terminal fields had a more diffuse distribution following substantia innominata than following diagonal band injections. No clear laminar pattern of termination was observed. However the density of terminals was higher in layers IV, V and VI than in layers I, II and III. Since the conjugate used is not taken up by fibers of passage, this pattern of connection is believed to reflect the organization of the projection of the nucleus of the diagonal band and of the substantia innominata to the cerebral cortex.

Animals↗

Acetylcholine excites identified septo-hippocampal neurons in the rat.

Neurons of the medial septum-nucleus of the diagonal band of Broca (vertical limb) area were identified as septo-hippocampal neurons by antidromic electrical activation in anesthetized rats. A large majority of these presumably cholinergic neurons could be excited by the iontophoretic application of acetylcholine or cholinergic agonists such as carbachol. The acetylcholine-induced excitations were readily antagonized by atropine. These results suggest that cholinergic neurons can be excited by their own transmitter, i.e. acetylcholine.

Acetylcholine↗