Evidence map›Paper›PMID 39425753›Full record

ArticleMolecular biology reports2024

Progesterone increases metabolism via the pentose phosphate pathway in bovine uterine epithelial cells.

Malia D Berg, Camila U Braz, Matthew Dean

Abstract read
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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

8 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

3 authors.

Malia D BergDepartment of Animal Science, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Camila U BrazDepartment of Animal Science, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Matthew DeanDepartment of Animal Science, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA. mjdean@illinois.edu.

Funding

Deciphering the Roles of Endometrial Glycogen Reserves and the Impact of Obesity on FertilityR01HD111706 · NICHD · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Matthew J Dean · 2023 to 2026
$1.6M
The Role of Uterine Glycogen in Establishing a Successful PregnancyR21HD112772 · NICHD · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI DEAN, MATTHEW J · 2023 to 2023
$328k
NICHD NIH HHS R01 HD111706NICHD NIH HHS R21 HD112772NIH HHS R21HD112772USDA NIFA ILLU-538-949
6 · The paper itself

Abstract

backgroundDuring early pregnancy, glucose is essential for the uterine epithelium and the developing embryo. In cows, progesterone increases the secretion of glucose into the uterine lumen. The uterine epithelium can convert glucose to fructose, but other fates of glucose in the uterine epithelium have been sparsely investigated. Therefore, our objective was to investigate how progesterone influences glucose metabolism in immortalized bovine uterine epithelial (BUTE) cells.

methodsBUTE cells were grown to 80% confluence and treated with vehicle (DMSO) or 10 µM progesterone for 24 h. Cells were collected and analyzed. Immunohistochemistry was performed on endometrial samples collected from the bovine endometrium on days 1 and 11 of the reproductive cycle.

resultsProgesterone treatment increased glucose consumption of BUTE cells. RNAseq identified 3,072 genes regulated by progesterone. KEGG analysis indicated that progesterone altered genes associated with metabolic pathways and glutathione metabolism. Manually examining genes unique to specific glucose metabolic pathways identified an increase in the rate-limiting enzyme in the pentose phosphate pathway-glucose-6-phosphate dehydrogenase. Functionally, a major product of the pentose phosphate pathway is NADPH, and progesterone treatment increased NADPH levels in BUTE cells. In cows, immunohistochemistry confirmed that glucose-6-phosphate dehydrogenase levels were higher in the uterine epithelium in the luteal phase when progesterone concentrations are high.

conclusionsProgesterone increased glucose-6-phosphate dehydrogenase expression and metabolism via the pentose phosphate pathway in the bovine uterine epithelium. This metabolism could provide substrates for cell proliferation, molecules to be secreted into the uterine lumen, or maintain reduction/oxidation balance in the uterine epithelium.

Indexed as

EndometriumEpithelial CellsGlucoseGlucosephosphate DehydrogenasePentose Phosphate PathwayProgesteroneUterusAnimalsCattleFemaleNADPGlucoseGlucosephosphate DehydrogenaseNADPProgesteroneCowGlucose-6-phosphate dehydrogenaseProgesteroneUterus

Identifiers

PMID39425753
PMCPMC11490429

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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.