Literature DB >> 8309542

Action of endogenous oxytocin within the paraventricular or supraoptic nuclei: a powerful link in the regulation of the bursting pattern of oxytocin neurons during the milk-ejection reflex in rats.

R C Lambert1, F C Moos, P Richard.   

Abstract

During suckling, the periodic and synchronous bursting activity of oxytocin neurons has been shown to be facilitated by oxytocin itself, acting via several target sites, including the magnocellular nuclei. To investigate the role of the endogenous oxytocin released within the magnocellular nuclei during the milk-ejection reflex in the rat, an oxytocin antagonist (50 microM solution of [d(CH2)5, Tyr(Me)2,Orn8]-vasotocin was pressure-injected into either one paraventricular or one supraoptic nucleus while recording the bursting pattern of oxytocin neurons within the injected nucleus and within a contralateral nucleus. The oxytocin antagonist was injected either during an ongoing milk-ejection reflex or during its facilitation induced by oxytocin (1 microliter of 1 microM solution injected into the third ventricle, i.e. 1 ng). During an ongoing milk-ejection reflex, injections of the oxytocin antagonist (10 nl of 50 microM solution, i.e. 50 ng) into the paraventricular or supraoptic nucleus decreased (more than 20% change) the burst amplitude (total number of spikes/burst) of neurons within the injected nucleus in 100% of tests, and simultaneously of contralateral neurons in 68% of tests. Burst periodicity of the entire population was also decreased in 50% of tests whatever the nucleus injected, but burst desynchronization was never observed. Successive injections of minute volumes of oxytocin (10 nl of 10 microM solution, i.e. 0.1 ng) into the paraventricular or supraoptic nucleus (which will progressively affect a greater number of neurons) first increased burst amplitude of oxytocin neurons within the injected nucleus and then increased simultaneously burst amplitude of contralateral neurons and burst frequency of the whole oxytocin neuron population. All these results suggest that the recruitment of a critical number of oxytocin neurons within one nucleus induces changes in the bursting activity of the oxytocin neurons in the four magnocellular nuclei. Within the minute following an intracerebroventricular oxytocin injection, the oxytocin antagonist injected into the supraoptic nucleus not only prevented the oxytocin-induced facilitation but also completely interrupted the milk-ejection reflex. When injected into the paraventricular nucleus, the oxytocin antagonist was less efficient: it decreased the oxytocin-induced facilitation but the reflex was not blocked. Similar partial inhibitory effect (decrease in burst amplitude and burst frequency) was also observed when the oxytocin antagonist was injected into the supraoptic nucleus after facilitation of the milk-ejection reflex by intracerebroventricular oxytocin injection. In conclusion, endogenous oxytocin released within the magnocellular nuclei during suckling represents a necessary link of the neuronal network regulating the bursting activity of oxytocin neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8309542     DOI: 10.1016/0306-4522(93)90046-i

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  23 in total

1.  Ca(2+) and frequency dependence of exocytosis in isolated somata of magnocellular supraoptic neurones of the rat hypothalamus.

Authors:  Brandi L Soldo; David R Giovannucci; Edward L Stuenkel; Hylan C Moises
Journal:  J Physiol       Date:  2003-11-28       Impact factor: 5.182

2.  Short-term potentiation of mEPSCs requires N-, P/Q- and L-type Ca2+ channels and mitochondria in the supraoptic nucleus.

Authors:  Michelle E Quinlan; Christian O Alberto; Michiru Hirasawa
Journal:  J Physiol       Date:  2008-05-08       Impact factor: 5.182

Review 3.  Multiple signalling modalities mediated by dendritic exocytosis of oxytocin and vasopressin.

Authors:  Mike Ludwig; Javier Stern
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2015-07-05       Impact factor: 6.237

4.  Vasopressin regularizes the phasic firing pattern of rat hypothalamic magnocellular vasopressin neurons.

Authors:  L Gouzènes; M G Desarménien; N Hussy; P Richard; F C Moos
Journal:  J Neurosci       Date:  1998-03-01       Impact factor: 6.167

Review 5.  Performance, properties and plasticity of identified oxytocin and vasopressin neurones in vitro.

Authors:  W E Armstrong; L Wang; C Li; R Teruyama
Journal:  J Neuroendocrinol       Date:  2010-02-20       Impact factor: 3.627

6.  GABA-induced facilitation of the periodic bursting activity of oxytocin neurones in suckled rats.

Authors:  F C Moos
Journal:  J Physiol       Date:  1995-10-01       Impact factor: 5.182

Review 7.  Electrophysiological properties of identified oxytocin and vasopressin neurones.

Authors:  William E Armstrong; Robert C Foehring; Matthew K Kirchner; Celia D Sladek
Journal:  J Neuroendocrinol       Date:  2019-02-14       Impact factor: 3.627

8.  Retrograde regulation of GABA transmission by the tonic release of oxytocin and endocannabinoids governs postsynaptic firing.

Authors:  Stéphane H R Oliet; Dinara V Baimoukhametova; Richard Piet; Jaideep S Bains
Journal:  J Neurosci       Date:  2007-02-07       Impact factor: 6.167

9.  Rapid preconcentration for liquid chromatography-mass spectrometry assay of trace level neuropeptides.

Authors:  Ying Zhou; Omar S Mabrouk; Robert T Kennedy
Journal:  J Am Soc Mass Spectrom       Date:  2013-04-17       Impact factor: 3.109

10.  A New Population of Parvocellular Oxytocin Neurons Controlling Magnocellular Neuron Activity and Inflammatory Pain Processing.

Authors:  Marina Eliava; Meggane Melchior; H Sophie Knobloch-Bollmann; Jérôme Wahis; Miriam da Silva Gouveia; Yan Tang; Alexandru Cristian Ciobanu; Rodrigo Triana Del Rio; Lena C Roth; Ferdinand Althammer; Virginie Chavant; Yannick Goumon; Tim Gruber; Nathalie Petit-Demoulière; Marta Busnelli; Bice Chini; Linette L Tan; Mariela Mitre; Robert C Froemke; Moses V Chao; Günter Giese; Rolf Sprengel; Rohini Kuner; Pierrick Poisbeau; Peter H Seeburg; Ron Stoop; Alexandre Charlet; Valery Grinevich
Journal:  Neuron       Date:  2016-03-03       Impact factor: 17.173

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