Evidence map›Paper›PMID 18812459›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2008

Central blockade of oxytocin receptors during mid-late gestation reduces amplitude of slow afterhyperpolarization in supraoptic oxytocin neurons.

R Teruyama, D L Lipschitz, L Wang, G R Ramoz, W R Crowley, S L Bealer, W E Armstrong

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Chronic hyperosmotic stress converts GABAergic inhibition into excitation in vasopressin and oxytocin neurons in the rat.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  11. Article
  12. Oxytocin release in magnocellular nuclei: neurochemical mediators and functional significance during gestation.American journal of physiology. Regulatory, integrative and comparative physiology · 2010
    Review
  13. Review
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

7 authors at 2 institutions in 1 country.

R TeruyamaDepartment of Anatomy and Neurobiology, University of Tennessee, Health Science Center, Memphis, Tennessee 38163, USA. rteruyam@utmem.edu
D L Lipschitz
L Wang
G R Ramoz
W R Crowley
S L Bealer
W E Armstrong
University of Utah · USUniversity of Tennessee Health Science Center · US

Funding

CENTRAL CONTROL OF OXYTOCIN RELEASE DURING GESTATIONR01HD038243 · NICHD · UNIVERSITY OF UTAH · PI BEALER, STEVEN BEALER · 2000 to 2008
$2.1M
Electrophysiological Correlates of Vasopressin SecretionR01NS023941 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ARMSTRONG, WILLIAM E · 1986 to 2009
$1.8M
Plasticity of Oxytocin Neurons During LactationR01HD041002 · NICHD · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ARMSTRONG, WILLIAM E · 2001 to 2005
$1.0M
Electrophysiological Correlates of Vasopressin ReleaseR56NS023941 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ARMSTRONG, WILLIAM E · 2011 to 2011
$354k
NICHD NIH HHS R01-HD-038243NICHD NIH HHS R01-HD-41002NINDS NIH HHS NS-23941
6 · The paper itself

Abstract

The neurohypophysial hormone oxytocin (OT), synthesized in magnocellular paraventricular (PVN) and supraoptic (SON) nuclei, is well known for its effects in lactation. Our previous studies showed that central OT receptor (OTR) binding is increased during gestation and that blockade of central OTRs, specifically during mid-late gestation, causes a delay in OT release during suckling and reduces weight gain in pups, suggesting decreased milk delivery. In the present study, we tested whether central OTR blockade during late gestation disrupts the gestation-related plasticity in intrinsic membrane properties. Whole cell current-clamp recordings were performed in OT neurons from pregnant rats (19-22 days in gestation) that were infused with an OTR antagonist (OTA) or artificial cerebrospinal fluid (aCSF) and from virgin rats infused with aCSF into the third ventricle via an osmotic minipump beginning on days 12-14 of gestation. The amplitudes of both Ca(2+)-dependent afterhyperpolarizations (AHPs), an apamin-sensitive medium AHP (mAHP) and an apamin-insensitive slow AHP (sAHP), were significantly increased during late gestation in control pregnant animals. However, the amplitude of the sAHP from pregnant rats treated with the OTA was significantly smaller than that of pregnant control rats and similar to that of virgins. These results indicate that the diminished efficiency in lactation due to OTR blockade may be partly a result of an altered sAHP that would shape OT bursting. These findings suggest that central actions of OT during late gestation are necessary for programming the plasticity of at least some of the intrinsic membrane properties in OT neurons during lactation.

Indexed as

Action PotentialsAnimalsApaminElectrophysiologyFemaleGestational AgeHypothalamus, AnteriorLactationMembrane PotentialsNeuronal PlasticityNeuronsOrnipressinOxytocinPregnancyRatsReceptors, OxytocinApaminOrnipressinOxytocinReceptors, OxytocinVasopressinsvasotocin, desGly(NH2)(9)d(CH2)5-Tyr(Me)(2)-Thr(4)-Orn(8)-

Identifiers

PMID18812459
PMCPMC2584811
OpenAlexW2126113502

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.