Evidence mapPaperPMID 40827403Full record

ReviewActa physiologica (Oxford, England)2025

AMPK: Accumulating Evidence in Support of its role in Dual Regulation of Vascular Function and Metabolism During Human Pregnancy.

Lorna G Moore, Stephanie R Wesolowski, Ramón A Lorca, Colleen G Julian

Abstract readReview
In one paragraph

Review in Acta physiologica (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lorna G MooreDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.ORCID https://orcid.org/0000-0001-5637-0025
Stephanie R WesolowskiSection of Neonatology, Department of Pediatrics, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.
Ramón A LorcaDivision of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.
Colleen G JulianDepartment of Biomedical Informatics, University of Colorado Denver School of Medicine, Aurora, Colorado, USA.

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · UNIVERSITY OF COLORADO DENVER · 1995 to 2025
$7.7M
Insulin and nutrient actions in the FGR fetal liverR01DK108910 · UNIVERSITY OF COLORADO DENVER · 2025 to 2025
$709k
Effects of chronic hypoxia and AMPK activation on uteroplacental perfusion, placental metabolism and the regulation of fetal growthR01HD088590 · UNIVERSITY OF COLORADO DENVER · 2025 to 2025
$677k
Genetic Regulation of Hypoxia-Induced IUGRR01HL079647 · UNIVERSITY OF COLORADO DENVER · 2005 to 2005
$442k
NHLBI NIH HHS R01 HL079647NHLBI NIH HHS R01 HL138181NICHD NIH HHS R01 HD088590NIDDK NIH HHS P30 DK048520NIDDK NIH HHS R01 DK108910NIH HHS DK108910NIH HHS HD088590NIH HHS HL079647NIH HHS HL138181
6 · The paper itself

Abstract

Adenosine monophosphate-activated protein kinase (AMPK) serves to match perfusion with metabolism. Since pregnancy necessitates significant changes in both perfusion and metabolism for supporting fetal growth, surprising is that AMPK has received scant attention during pregnancy, perhaps due to the complexity of its actions and multiple maternal, placental, and fetal targets. Here we review human as well as experimental animal studies documenting AMPK activation's broad-ranging maternal effects. Emphasized are those affecting vascular control and blood flow to the uteroplacental circulation under conditions of chronic hypoxia. Time and dosage-dependent effects on the placenta and the fetus are also reviewed, revealing that AMPK activation affects all three-maternal, placental, and fetal-pregnancy compartments. We point to the need for an integrated study of AMPK's effects in each compartment during normal as well as fetal growth-restricted (FGR) pregnancies. Since there are currently no therapies for FGR apart from early delivery, whereas there are drugs or nutritional substances activating AMPK approved for human use, such agents may represent new treatments. However, understanding their molecular mechanisms and specific actions in pregnancy compartments is required before conducting such trials.

Indexed as

AMP-Activated Protein KinasesPlacentaAnimalsFemaleFetal Growth RetardationFetusHumansPlacental CirculationPregnancyAMP-Activated Protein Kinasesblood flowcarbohydrate metabolismfetal growth restrictionhigh altitudehypoxiapreeclampsia

Identifiers

PMID40827403
PMCPMC12643132

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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 Socratic graph.