magnocellular nuclei
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2021 ◽  
Vol 111 ◽  
pp. 101883
Author(s):  
Artur Pałasz ◽  
Aleksandra Suszka-Świtek ◽  
Andrzej Kaśkosz ◽  
Danuta Plewka ◽  
Katarzyna Bogus ◽  
...  


2011 ◽  
Vol 334 (12) ◽  
pp. 855-862 ◽  
Author(s):  
Saliha Ouali-Hassenaoui ◽  
Mounira Bendjelloul ◽  
Aicha Dekar ◽  
Dionysia Theodosis


Endocrinology ◽  
2008 ◽  
Vol 149 (9) ◽  
pp. 4279-4288 ◽  
Author(s):  
Gérard Alonso ◽  
Evelyne Gallibert ◽  
Chrystel Lafont ◽  
Gilles Guillon

We have previously shown that hyperosmotic stimulation of adult Wistar rats induces local angiogenesis within hypothalamic magnocellular nuclei, in relation to the secretion of vascular endothelial growth factor (VEGF) by the magnocellular neurons. The present study aimed at understanding how osmotic stimulus relates to increased VEGF secretion. We first demonstrate a correlation between increased VEGF secretion and local hypoxia. Osmotic stimulation is known to stimulate the metabolic activity of hypothalamic magnocellular neurons producing arginine vasopressin (AVP) and to increase the secretion of AVP, both by axon terminals into the circulation and by dendrites into the extracellular space. In AVP-deficient Brattleboro rats, the dramatic activation of magnocellular hypothalamic neurons failed to induce hypoxia, VEGF expression, or angiogenesis, suggesting a major role of hypothalamic AVP. A possible involvement of dendritic AVP release is supported by the findings that 1) hypoxia and angiogenesis were not observed in non osmotically stimulated Wistar rats in which circulating AVP was increased by the prolonged infusion of exogenous AVP, 2) contractile arterioles afferent to the magnocellular nuclei were strongly constricted by the perivascular application of AVP via V1a receptors (V1a-R) stimulation, and 3) after the intracerebral or ip administrations of selective V1a-R antagonists to osmotically stimulated rats, hypothalamic hypoxia and angiogenesis were or were not inhibited, respectively. Together, these data strongly suggest that the angiogenesis induced by osmotic stimulation relates to tissue hypoxia resulting from the constriction of local arterioles, via the stimulation of perivascular V1a-R by AVP locally released from dendrites.



2006 ◽  
Vol 291 (1) ◽  
pp. R102-R111 ◽  
Author(s):  
Cherif Boudaba ◽  
Jeffrey G. Tasker

Magnocellular neurons of the supraoptic nucleus (SON) and paraventricular nucleus (PVN) display bursting activity that is synchronized under certain conditions. They receive excitatory synaptic inputs from intrahypothalamic glutamate circuits, some of which are activated by norepinephrine. Ascending noradrenergic afferents and intrahypothalamic glutamate circuits may be responsible for the generation of synchronous bursting among oxytocin neurons and/or asynchronous bursting among vasopressin neurons located in the bilateral supraoptic and paraventricular nuclei. Here, we tested whether magnocellular neurons of the PVN receive excitatory synaptic input from the contralateral PVN and the region of the retrochiasmatic SON (SONrx) via norepinephrine-sensitive internuclear glutamate circuits. Whole cell patch-clamp recordings were performed in PVN magnocellular neurons in coronal hypothalamic slices from male rats, and the ipsilateral SONrx region and contralateral PVN were stimulated using electrical and chemical stimulation. Electrical and glutamate microdrop stimulation of the ipsilateral SONrx region or contralateral PVN elicited excitatory postsynaptic potentials/currents (EPSP/Cs) in PVN magnocellular neurons mediated by glutamate release, revealing internuclear glutamatergic circuits. Microdrop application of norepinephrine also elicited EPSP/Cs, suggesting that these circuits could be activated by activation of noradrenergic receptors. Repetitive electrical stimulation and drop application of norepinephrine, in some cases, elicited bursts of action potentials. Our data reveal glutamatergic synaptic circuits that interconnect the magnocellular nuclei and that can be activated by norepinephrine. These internuclear glutamatergic circuits may provide the functional architecture to support burst generation and/or burst synchronization in hypothalamic magnocellular neurons under conditions of activation.



2006 ◽  
Vol 2 (1) ◽  
pp. 51-58 ◽  
Author(s):  
AUDE PANATIER ◽  
STEPHANE H.R. OLIET

The supraoptic (SON) and paraventricular (PVN) magnocellular nuclei of the hypothalamus undergo reversible anatomical remodeling under conditions of intense secretion of neurohypophysial hormones, such as lactation and chronic dehydration. This morphological plasticity is characterized by a pronounced reduction in astrocytic coverage of neurons, which results in an increased number and extent of directly juxtaposed somatic and dendritic surfaces. As a consequence, astrocyte-mediated clearance of glutamate from the extracellular space is altered, which causes an increased concentration and range of action of the excitatory amino acid in the extracellular space. This leads to a reduction of synaptic efficacy at excitatory and inhibitory inputs through the activation of presynaptic metabotropic glutamate receptors. By contrast, the action of gliotransmitters released from astrocytes and acting on adjacent magnocellular neurons is limited during such anatomical remodeling. This includes glia-derived ATP mediating potentiation of glutamatergic transmission, a process compromised by the neuronal-glial reorganization. Together, these studies on hypothalamic magnocellular nuclei provide new insights on the contribution of glial cells on neuronal activity.







2002 ◽  
Vol 949 (1-2) ◽  
pp. 112-121 ◽  
Author(s):  
Seiji Miyata ◽  
Ichiro Shinga ◽  
Katsutoshi Taguchi ◽  
Toshihiro Nakashima ◽  
Toshikazu Kiyohara ◽  
...  


2001 ◽  
Vol 12 (10) ◽  
pp. 960-969 ◽  
Author(s):  
J. Badaut ◽  
A. Nehlig ◽  
J.-M. Verbavatz ◽  
M.-E. Stoeckel ◽  
M.-J. Freund-Mercier ◽  
...  


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