Literature DB >> 3612564

Regulation of the milk ejection reflex in the rat.

R E Dyball, G Leng.   

Abstract

Extracellular recordings were made from neurones in or near the supraoptic nucleus in suckled lactating rats under urethane anaesthesia to investigate the mechanism by which the firing of oxytocin cells is synchronized during reflex milk ejection. Cells synaptically driven but not antidromically activated by neural stalk stimulation, which thus probably receive an afferent input from supraoptic neurones, were classified as 'regular' or 'bursters' on the basis of their spontaneous electrical activity. The majority (twelve out of eighteen) of synaptically excited cells (o.d.+) were bursters and the majority of inhibited (o.d.-) cells (eleven out of nineteen) were regular, but only one o.d.+ burster showed any change of activity (inhibition) before milk ejection. Putative oxytocin cells in suckled lactating rats showed a firing pattern between milk-ejection bursts which could not be distinguished from that of putative oxytocin cells in male animals. The mode interspike interval between milk ejections was 47.1 +/- 3.1 ms (mean +/- S.E. of mean) compared with 47.3 +/- 3.3 ms in male rats, and fewer than 1.4% of interspike intervals were less than 20 ms in duration. By contrast, within milk-ejection bursts 40% of interspike intervals were in the range 8-20 ms. Short trains (10 or 20) of pulses applied to the neural stalk at regular (5 min) intervals, in an attempt to simulate the initial part of the milk ejection burst, failed to trigger bursts. In only 2 of 150 tests was the interval between train and milk-ejection burst less than 10 s, and after the pulse train all but one cell showed reduced activity for 1-3 s. The trains of pulses were however not without effect: they significantly (P less than 0.01) enhanced the chance of a milk-ejection burst occurring within the next 2.5 min. Our observation that pulse trains do not trigger bursts suggests that local positive feed-back mechanisms are not responsible for orchestrating the activation of oxytocin cells during the milk-ejection reflex. Moreover, because spontaneous tiring pattern is the same in lactating and non-lactating rats, we found no evidence that the anatomical changes in the synaptic organization within the supraoptic nuclei in lactation have any influence on the firing of oxytocin cells. It is likely, however, since pulse trains alter the timing of milk ejections, that oxytocin released locally in the region of the supraoptic nucleus can influence reflex milk ejection.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3612564      PMCID: PMC1182935          DOI: 10.1113/jphysiol.1986.sp016283

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  26 in total

1.  Intercommunication in the rat supraoptic nucleus.

Authors:  G Leng; R E Dyball
Journal:  Q J Exp Physiol       Date:  1983-07

2.  Intrinsic inhibition in magnocellular neuroendocrine cells of rat hypothalamus.

Authors:  R D Andrew; F E Dudek
Journal:  J Physiol       Date:  1984-08       Impact factor: 5.182

3.  Synchronization of oxytocin cells in the hypothalamic paraventricular and supraoptic nuclei in suckled rats: direct proof with paired extracellular recordings.

Authors:  V Belin; F Moos; P Richard
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

Review 4.  Dynamic neuronal-glial interactions in hypothalamus and pituitary: implications for control of hormone synthesis and release.

Authors:  G I Hatton; L S Perlmutter; A K Salm; C D Tweedle
Journal:  Peptides       Date:  1984       Impact factor: 3.750

5.  Evidence for structural plasticity in the supraoptic nucleus of the rat hypothalamus in relation to gestation and lactation.

Authors:  D T Theodosis; D A Poulain
Journal:  Neuroscience       Date:  1984-01       Impact factor: 3.590

6.  Release of oxytocin and vasopressin by magnocellular nuclei in vitro: specific facilitatory effect of oxytocin on its own release.

Authors:  F Moos; M J Freund-Mercier; Y Guerné; J M Guerné; M E Stoeckel; P Richard
Journal:  J Endocrinol       Date:  1984-07       Impact factor: 4.286

7.  Evidence that oxytocin-secreting neurones are involved in the ultrastructural reorganisation of the rat supraoptic nucleus apparent at lactation.

Authors:  D T Theodosis; D A Poulain
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

8.  Electrophysiological evidence for facilitatory control of oxytocin neurones by oxytocin during suckling in the rat.

Authors:  M J Freund-Mercier; P Richard
Journal:  J Physiol       Date:  1984-07       Impact factor: 5.182

9.  Cytoarchitecture of the rat's supraoptic nucleus.

Authors:  J E Bruni; P M Perumal
Journal:  Anat Embryol (Berl)       Date:  1984

10.  Oxytocin-immunoreactive terminals synapse on oxytocin neurones in the supraoptic nucleus.

Authors:  D T Theodosis
Journal:  Nature       Date:  1985 Feb 21-27       Impact factor: 49.962

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  17 in total

1.  Responses of magnocellular neurons to osmotic stimulation involves coactivation of excitatory and inhibitory input: an experimental and theoretical analysis.

Authors:  G Leng; C H Brown; P M Bull; D Brown; S Scullion; J Currie; R E Blackburn-Munro; J Feng; T Onaka; J G Verbalis; J A Russell; M Ludwig
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

2.  Measuring spike coding in the rat supraoptic nucleus.

Authors:  G S Bhumbra; R E J Dyball
Journal:  J Physiol       Date:  2003-11-07       Impact factor: 5.182

3.  An electrophysiological analysis of the hippocampal projections to the neurosecretory cells of the supraoptic nucleus of the hypothalamus and the neurons of the perinuclear zone of rats.

Authors:  N P Prutskova
Journal:  Neurosci Behav Physiol       Date:  1992 Nov-Dec

4.  Spike coding from the perspective of a neurone.

Authors:  G S Bhumbra; R E J Dyball
Journal:  Cogn Process       Date:  2005-08-12

5.  Secretory cells of the supraoptic nucleus have central as well as neurohypophysial projections.

Authors:  A N Inyushkin; H O Orlans; R E J Dyball
Journal:  J Anat       Date:  2009-10       Impact factor: 2.610

6.  Electrophysiological analysis of the morphofunctional organization of the limbic control of magnocellular neurosecretory nuclei in the rat hypothalamus.

Authors:  N P Prutskova
Journal:  Neurosci Behav Physiol       Date:  1998 Jan-Feb

7.  Milk ejection in mice LG/J x SM/J.

Authors:  Carolina P Góes; Bruno Sauce; Andrea C Peripato
Journal:  Mamm Genome       Date:  2012-10-07       Impact factor: 2.957

8.  Electrophysiological characteristics of immunochemically identified rat oxytocin and vasopressin neurones in vitro.

Authors:  W E Armstrong; B N Smith; M Tian
Journal:  J Physiol       Date:  1994-02-15       Impact factor: 5.182

9.  Activity dependence and functional role of the apamin-sensitive K+ current in rat supraoptic neurones in vitro.

Authors:  K Kirkpatrick; C W Bourque
Journal:  J Physiol       Date:  1996-07-15       Impact factor: 5.182

Review 10.  Physiological regulation of magnocellular neurosecretory cell activity: integration of intrinsic, local and afferent mechanisms.

Authors:  C H Brown; J S Bains; M Ludwig; J E Stern
Journal:  J Neuroendocrinol       Date:  2013-08       Impact factor: 3.627

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