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M Lavialle

Publications and source records attributed to M Lavialle.

10 recordsLinked to original sources

Dietary docosahexaenoic acid [22: 6(n-3)] as a phospholipid or a triglyceride enhances the potassium chloride-evoked release of acetylcholine in rat hippocampus.

We demonstrated previously that a dietary-induced depletion of docosahexaenoic acid (DHA) in cerebral phospholipids increases the spontaneous release of acetylcholine (Ach) in the rat hippocampus and reduces its potassium chloride evoked-release. In the present study, we investigated the effects in rats of DHA-enriched diets supplied by egg phospholipids (E-PL) or tuna oil (TO) on the PUFA in hippocampus membranes and on the synaptic release of Ach. Control rats were fed 3 g/kg of the DHA precursor, alpha-linolenic acid (LNA). Chronically (n-3) PUFA-deficient females were fed, starting 2 wk before mating, the deficient diet, a control diet, or a purified diet supplying 1, 2, or 3 g DHA/kg diet as E-PL or TO. Experiments were performed on the adult male progeny fed the same diet as their dams throughout life. The form of dietary DHA (TO or E-PL) did not influence its incorporation into the hippocampus. The 1 g DHA/kg diets allowed maximal incorporation into phosphatidylethanolamine (PE), but 2 g DHA/kg diet was needed for phosphatidylcholine (PC). A minimum of 2 g DHA/kg was needed to decrease the basal Ach release and to enhance the stimulated release to that of the control; the Ach release of the 1 g/kg DHA-groups did not differ from that of the deficient group. This suggests that >1 g DHA/kg diet is needed to ensure PUFA incorporation into PE and PC, and basal and stimulated Ach release in the rat hippocampus equivalent to the control group fed only LNA. PUFA incorporation into the hippocampus depends mainly on the PUFA concentration of the diet, not on the form of dietary DHA.

Acetylcholine↗

Modifications of retinal afferent activity induce changes in astroglial plasticity in the hamster circadian clock.

The circadian clock, located in the suprachiasmatic nucleus (SCN) of the hypothalamus in mammals, exhibits astroglial plasticity indicated by GFAP expression over the 24-h period. In this study, we evaluated the role of neuronal retinal input in the observed changes. Modifications of retinal input, either by rearing animals under darkness (DD) or under constant light (LL), or by suppressing afferent input (bilateral enucleation), induced drastic changes in astroglial plasticity. In enucleated animals, a dramatic decrease in GFAP expression was evident in the area of the SCN deprived of retinal projections, whereas persistence of a rhythmic variation was in those areas still exhibiting GFAP expression. By contrast, no changes in astrocytic plasticity were detected in hamsters maintained under LL. These data suggest two fundamental roles for astrocytes within the SCN: (1) to regulate and mediate glutamate released by retinal terminals throughout the neuronal network to facilitate photic signal transmission; (2) to contribute to synchronization between suprachiasmatic neurons.

Animals↗

Daily changes of cytochrome oxidase activity within the suprachiasmatic nucleus of the Syrian hamster.

Cytochrome oxidase (CO) activity was studied over a 24-h period in the Syrian hamster suprachiasmatic nucleus (SCN) (site of the biological clock), anterior hypothalamic area (AHA), and motor cortex. The SCN CO activity was highest at the middle of the day (Zeitgeber time (ZT) 05), decreased at the end of the light period (ZT 10) and continued at a low level during the night (ZT 13, 16, 21.5 and 24). AHA and motor cortex showed a similar profile of CO activity and no changes of CO activity were found in animals maintained under darkness (DD). We propose that photic input plays a role in the SCN neuronal activity that modulates metabolic activity on this area.

Animals↗

A method to quantify glial fibrillary acidic protein immunoreactivity on the suprachiasmatic nucleus.

The aim of the present study was to develop a quantitative method to measure the immunoreactivity of the glial fibrillary acidic protein on the suprachiasmatic nucleus of hamster. For this purpose, optical microscopy images from brain sections processed for glial fibrillary acidic protein immunostaining were digitised under different light conditions. Image treatment and immunoreactivity quantification were performed following five different methods using the program Adobe Photoshop. The results were analysed in order to determine the ability of each method to differentiate immunoreactivity levels, and their susceptibility to the light conditions during image acquisition. Four of the five methods were found to be susceptible to the tested light conditions, while the other was not. This last method, which permits detection of differences in immunoreactivity between the different sections, was considered for further quantification of glial fibrillary acidic protein immunoreactivity on the suprachiasmatic nucleus.

Animals↗

[The suprachiasmatic nucleus: cellular approach to clock functioning].

The hypothalamic suprachiasmatic nucleus (SCN), the circadian clock in mammals, generates and maintains a variety of daily rhythms. The present review is an attempt to synthesis experimental data on the anatomical organisation and cellular activities within SCN. The clock exhibits an endogenous rhythmic activity and can also be entrained by environmental synchronisers such as the light/dark cycle. It can be also influenced by internal signals such as the rhythmic secretion of melatonin which is under control of SCN activity. This tiny structure contains a variety of peptides organised in a specific distribution. It receives three main inputs from the retina (glutamate), the intergeniculate leaflet (NPY) and the dorsal raphe (serotonin). VIP containing cells located in the ventral part of SCN receive all these afferences and innervate the whole structure. VIP, PHI and GRP are likely implicated in the entrainment of the clock. The vasopressin (VP) cells exhibiting an endogenous rhythmic synthesis are considered as an output of the clock. The specific induction of immediate early genes (c-fos, jun B) within SCN by light pulses during the subjective night suggests the participation of these genes in the process of cellular entrainment by the photic input. The demonstration of a rhythmic astrocytic activity within SCN suggests an active involvement of this cellular population in the functioning of the clock facilitating or not neuronal communication. Cellular disturbances such as a decrease in VIP or VP cell population, reduction in the amplitude of functional cellular rhythms, astrocytic proliferation could explain some pathologies observed with ageing.

Animals↗

Developmental study in the circadian clock of the golden hamster: a putative role of astrocytes.

The hypothalamic suprachiasmatic nuclei (SCN) house the circadian clock in the mammalian brain. A glial fibrillary acidic protein immunoreactivity (GFAP-ir) distribution rhythm has been observed in the SCN of adult Syrian hamster. The implication of astrocytes in photic entrainment was analyzed through developmental studies of the photic pathway and of SCN astrocytes appearance. Using anterograde tracing we studied the timing of penetration of the retinohypothalamic tract (RHT) fibers into the SCN. Using c-fos induction by light we followed the maturation of RHT synapses in the SCN. When RHT terminals reach the SCN, c-fos induction can be obtained. Using GFAP immunoreactivity we demonstrated that the number of astrocytes increased in parallel with RHT development from PN5 to PN15. At PN15, a time when pups can shift from maternal to photic entrainment, RHT terminals and GFAP-ir exhibit an adult-like pattern. One demonstrated role of astrocytes is to control extracellular glutamate concentration. Glutamate is the neurotransmitter released at RHT terminals; its content fluctuates according to a circadian rhythm within the SCN. Thus the present data tend to indicate that SCN astrocytes are participating in the circadian rhythm of SCN glutamate content.

Aging↗

Circadian fluctuations in GFAP distribution in the Syrian hamster suprachiasmatic nucleus.

We examined the possibility that astrocytes reflect mammalian circadian rhythmicity by observing the astrocytes pattern using anti-glial fibrillary acidic protein (GFAP), within the suprachiasmatic nucleus of the Syrian hamster over the 24 h cycle. Our results reveal daily systematic changes in the distribution of GFAP-immunoreactivity (GFAP-ir) both in the light/dark cycle and in constant darkness. This rhythm is characterized by a change of the GFAP-ir distribution from a network pattern to isolated cells. Such a rhythm is in synchrony with the rhythm in SCN glucose consumption which we have previously reported. This is the first time a circadian rhythm in suprachiasmatic astrocytes has been observed, indicating that GFAP-ir can be used as a novel index of clock activity.

Animals↗

The 24-h rhythm of metabolic activity of the cockroach circadian pacemaker.

In the cockroach, Leucophaea maderae, the optic lobes contain a circadian pacemaker. The metabolic activity of optic lobe neuropils was measured at 17 time points over a 24-h period in constant darkness, using cytochrome oxidase activity as functional marker. The results revealed a clear 24-h energy metabolism rhythm in neuropils and particularly in the lobula plate, a part of the region which is assumed to include a circadian pacemaker in this species.

Animals↗

Anatomical aspects of glia-synapse interaction: the perisynaptic glial sheath consists of a specialized astrocyte compartment.

Amongst several forms of glia-neuronal communication, glia-synaptic interaction appears particularly interesting in the light of the well-known examples of two-way signaling between neurons and astrocytes. We review recent structural and physiological evidence showing that the structural correlate of glia-synaptic interaction is the peripheral astrocyte process (PAP) positioned next to the synaptic cleft. The structural and functional properties of these processes suggest that the PAP represents a separate astroglial compartment, in particular since it is characterized by the restricted localization of the actin-binding ERM protein ezrin. The structural properties of PAPs and this protein form the basis of rapid morphological changes of PAPs. The physiological relevance of PAP plasticity is illustrated by the example of the suprachiasmatic nucleus, where astrocytes display a high degree of activity-dependent plasticity reflecting circadian time.

Animals↗