Evidence map›Paper›PMID 26630389›Full record

ArticlePsychoneuroendocrinology2016

CRF-R1 activation in the anterior-dorsal BNST induces maternal neglect in lactating rats via an HPA axis-independent central mechanism.

Stefanie M Klampfl, Paula J Brunton, Doris S Bayerl, Oliver J Bosch

Open access · hybridAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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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

4 authors at 2 institutions in 2 countries.

Stefanie M KlampflDepartment of Behavioural and Molecular Neurobiology, University of Regensburg, 93053 Regensburg, Germany. Electronic address: stefanie.klampfl@ubc.ca.
Paula J BruntonDivision of Neurobiology, The Roslin Institute and R(D)SVS, University of Edinburgh, Midlothian EH25 9RG, UK. Electronic address: P.J.Brunton@ed.ac.uk.
Doris S BayerlDepartment of Behavioural and Molecular Neurobiology, University of Regensburg, 93053 Regensburg, Germany. Electronic address: doris.bayerl@ur.de.
Oliver J BoschDepartment of Behavioural and Molecular Neurobiology, University of Regensburg, 93053 Regensburg, Germany. Electronic address: oliver.bosch@ur.de.
University of Regensburg · DERoslin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J004332/1Biotechnology and Biological Sciences Research Council BBS/E/D/20251969
6 · The paper itself

Abstract

Adequate maternal behavior in rats requires minimal corticotropin-releasing factor receptor (CRF-R) activation in the medial-posterior bed nucleus of the stria terminalis (mpBNST). Based on the architectural heterogeneity of the BNST and its distinct inter-neural connectivity, we tested whether CRF-R manipulation in another functional part, the anterior-dorsal BNST (adBNST), differentially modulates maternal behavior. We demonstrate that in the adBNST, activation of CRF-R1 reduced arched back nursing (ABN) and nursing, whereas activation of CRF-R2 resulted in an initial reduction in nursing but significantly increased the incidence of ABN 5h after the treatment. Following stressor exposure, which is detrimental to maternal care, ABN tended to be protected by CRF-R1 blockade. Maternal motivation, maternal aggression, and anxiety were unaffected by any manipulation. Furthermore, under basal and stress conditions, activation of adBNST CRF-R1 increased plasma ACTH and corticosterone concentrations, whereas stimulation of adBNST CRF-R2 increased basal plasma ACTH and corticosterone concentrations, but blocked the stress-induced increase in plasma corticosterone secretion. Moreover, both the CRF-R1 and -R2 antagonists prevented the stress-induced increase in plasma corticosterone secretion. Importantly, elevated levels of circulating corticosterone induced by intra-adBNST administration of CRF-R1 or -R2 agonist did not impact maternal care. Finally, Crf mRNA expression in the adBNST was increased during lactation; however, Crfr1 mRNA expression was similar between lactating and virgin rats. In conclusion, maternal care is impaired by adBNST CRF-R1 activation, and this appears to be the result of a central action, rather than an effect of elevated circulating levels of CORT. These data provide new insights into potential causes of disturbed maternal behavior postpartum.

Indexed as

Adrenocorticotropic HormoneAnimalsCorticosteroneCorticotropin-Releasing HormoneCRF Receptor, Type 1FemaleHypothalamo-Hypophyseal SystemLactationMaleMaternal BehaviorPituitary-Adrenal SystemRatsReceptors, Corticotropin-Releasing HormoneSeptal NucleiAdrenocorticotropic HormoneCorticosteroneCorticotropin-Releasing HormoneCRF Receptor, Type 1CRF receptor type 2Receptors, Corticotropin-Releasing HormoneAnxietyBed nucleus of the stria terminalisCorticotropin-releasing factorHypothalamic–pituitary–adrenal axisMaternal behavior

Identifiers

PMID26630389
PMCPMC4712652
OpenAlexW2173349838

What OpenQuestion holds

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LicenceCC BY
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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.