Evidence map›Paper›PMID 34281190›Full record

ArticleInternational journal of molecular sciences2021

Plasticity in Intrinsic Excitability of Hypothalamic Magnocellular Neurosecretory Neurons in Late-Pregnant and Lactating Rats.

Michael R Perkinson, Rachael A Augustine, Gregory T Bouwer, Emily F Brown, Isaiah Cheong, Alexander J Seymour, Martin Fronius, Colin H Brown

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Michael R PerkinsonBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.
Rachael A AugustineBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.
Gregory T BouwerBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.
Emily F BrownBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.
Isaiah CheongBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.
Alexander J SeymourBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.
Martin FroniusDepartment of Physiology, School of Biomedical Sciences, University of Otago, P.O. Box 56, Dunedin 9054, New Zealand.
Colin H BrownBrain Health Research Centre, University of Otago, Dunedin 9054, New Zealand.ORCID 0000-0003-2305-846X

Funding

Royal Society Te Aparangi Marsden Fund UOO1602
6 · The paper itself

Abstract

Oxytocin and vasopressin secretion from the posterior pituitary gland are required for normal pregnancy and lactation. Oxytocin secretion is relatively low and constant under basal conditions but becomes pulsatile during birth and lactation to stimulate episodic contraction of the uterus for delivery of the fetus and milk ejection during suckling. Vasopressin secretion is maintained in pregnancy and lactation despite reduced osmolality (the principal stimulus for vasopressin secretion) to increase water retention to cope with the cardiovascular demands of pregnancy and lactation. Oxytocin and vasopressin secretion are determined by the action potential (spike) firing of magnocellular neurosecretory neurons of the hypothalamic supraoptic and paraventricular nuclei. In addition to synaptic input activity, spike firing depends on intrinsic excitability conferred by the suite of channels expressed by the neurons. Therefore, we analysed oxytocin and vasopressin neuron activity in anaesthetised non-pregnant, late-pregnant, and lactating rats to test the hypothesis that intrinsic excitability of oxytocin and vasopressin neurons is increased in late pregnancy and lactation to promote oxytocin and vasopressin secretion required for successful pregnancy and lactation. Hazard analysis of spike firing revealed a higher incidence of post-spike hyperexcitability immediately following each spike in oxytocin neurons, but not in vasopressin neurons, in late pregnancy and lactation, which is expected to facilitate high frequency firing during bursts. Despite lower osmolality in late-pregnant and lactating rats, vasopressin neuron activity was not different between non-pregnant, late-pregnant, and lactating rats, and blockade of osmosensitive ΔN-TRPV1 channels inhibited vasopressin neurons to a similar extent in non-pregnant, late-pregnant, and lactating rats. Furthermore, supraoptic nucleus ΔN-TRPV1 mRNA expression was not different between non-pregnant and late-pregnant rats, suggesting that sustained activity of ΔN-TRPV1 channels might maintain vasopressin neuron activity to increase water retention during pregnancy and lactation.

Indexed as

Action PotentialsAnimalsBasal Nucleus of MeynertFemaleHypothalamusLactationMilk EjectionNeuronsOxytocinParaventricular Hypothalamic NucleusPregnancyRatsSupraoptic NucleusVasopressinsOxytocinVasopressinslactationoxytocinpregnancysupraoptic nucleustransient receptor potential vanilloid channelvasopressin

Identifiers

PMID34281190
PMCPMC8268815

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.