Evidence map›Paper›PMID 40767381›Full record

ArticleJournal of neuroendocrinology2025

Mapping O-linked glycosylation in the rat hypothalamus in pregnancy and lactation.

Chantelle L Murrell, Zsuzsanna Barad, Rachel S Wallace, Jeffrey R Erickson, Colin H Brown, Rachael A Augustine

Abstract read
In one paragraph

Article in Journal of neuroendocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Chantelle L MurrellCentre for Neuroendocrinology, University of Otago, Dunedin, New Zealand.ORCID 0009-0004-4678-0601
Zsuzsanna BaradCentre for Neuroendocrinology, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-7223-8953
Rachel S WallaceDepartment of Physiology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.ORCID 0000-0003-3304-9524
Jeffrey R EricksonDepartment of Physiology, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.ORCID 0000-0001-5918-1991
Colin H BrownCentre for Neuroendocrinology, University of Otago, Dunedin, New Zealand.ORCID 0000-0003-2305-846X
Rachael A AugustineCentre for Neuroendocrinology, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-6201-1026

Funding

Health Research Council of New Zealand 14/568
6 · The paper itself

Abstract

Many maternal adaptations occur during pregnancy to support the metabolic demands of the developing fetus and to prepare for the continued metabolic demands of lactation. Among these maternal adaptations are changes in the hypothalamic areas that regulate energy homeostasis: the paraventricular nucleus (PVN), ventromedial hypothalamic nucleus (VMH) and arcuate nucleus (ARC). The adaptive changes in the PVN, VMH, and ARC are believed to be driven by reduced responsiveness to the satiety hormone, leptin, during pregnancy. However, increased maternal metabolism is supported by elevated circulating glucose levels in pregnancy, and glucose itself can alter cell function by O-linked N-acetylglucosamine (O-GlcNAc) post-translational modification of proteins (O-GlcNAcylation). Therefore, we hypothesized that O-GlcNAcylation would be increased within the hypothalamic brain areas that are involved in the maternal adaptations to the increased metabolic demands of pregnancy: the ARC, VMH, and PVN. We completed immunohistochemistry and western blotting for O-GlcNAc in the ARC, VMH, and PVN from non-pregnant, late-pregnant, and lactating rats. Unexpectedly, we found that the number of O-GlcNAc-expressing cells and the levels of O-GlcNAc protein expression were similar within each area in non-pregnant, late-pregnant, and lactating rats. However, western blot analysis showed that the specific proteins that were O-GlcNAcylated appeared to be different between the reproductive states within each area. Further work will be required to identify the specific proteins that are differentially O-GlcNAcylated in each of the areas during pregnancy and lactation to determine whether this might contribute to the maternal adaptations required to cope with the metabolic demands of pregnancy and lactation.

Indexed as

GlycosylationHypothalamusLactationN-AcetylglucosaminyltransferasesPregnancy, AnimalAnimalsBlotting, WesternFemalePregnancyRatsRats, Sprague-DawleyN-AcetylglucosaminyltransferasesOgt protein, mouseglucoselactationO‐linked N‐acetylglucosaminepregnancy

Identifiers

PMID40767381
PMCPMC12678011

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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.