Evidence map›Paper›PMID 40114299›Full record

ArticleBiology of reproduction2025

Delayed blastocyst development is associated with altered metabolism and proteome in male and female bovine embryos†.

Kyle J Fresa, Ming-Hao Cheng, Keira Y Larson, Alexandra A Crook, Anthony J Saviola, Raul A Gonzalez-Castro, Thomas W Chen, Elaine M Carnevale

Abstract read
In one paragraph

Article in Biology of reproduction, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Translational Fidelity Decline in the Aging Oocyte and Embryo Development.International journal of molecular sciences · 2026
    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

8 authors.

Kyle J FresaDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Ming-Hao ChengDepartment of Electrical and Computer Engineering, Colorado State University, Fort Collins, Colorado, USA.
Keira Y LarsonUniversity of Colorado School of Medicine Proteomics Core, Aurora, Colorado, USA.
Alexandra A CrookUniversity of Colorado School of Medicine Proteomics Core, Aurora, Colorado, USA.
Anthony J SaviolaUniversity of Colorado School of Medicine Proteomics Core, Aurora, Colorado, USA.
Raul A Gonzalez-CastroDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.
Thomas W ChenDepartment of Electrical and Computer Engineering, Colorado State University, Fort Collins, Colorado, USA.
Elaine M CarnevaleDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.

Funding

ARBL Translational Reproductive BiotechnologyCRC CSU College Research Council Bovine FoundationUSDA NIFA
6 · The paper itself

Abstract

Developmentally delayed embryos are associated with reduced implantation potential and live birth rates; however, inherent causes of delayed development are not well understood. Metabolism during preimplantation development is responsible for the production of energy and biosynthetic material to support growth, and disturbances to these pathways can reduce embryo viability. The present study utilized electrochemical microsensors to determine differences in rates for oxygen consumption, extracellular acidification, and hydrogen peroxide production between normal and slow-growing, male and female bovine blastocysts. In addition, pooled samples of blastocysts were subjected to proteomic analysis to determine differences in the abundance of proteins associated with metabolism between the sexes and developmental timing status. In comparison to blastocysts developing over a normal timespan, blastocysts forming 1-2 days later had a higher oxygen consumption rate, differences in abundance of electron transport complex proteins, and reduced abundance of biosynthetic enzymes when compared to blastocysts developing during a normal timeline. Embryo sex resulted in unique differences in metabolic enzyme abundance with potentially different contributions to delayed development. In addition, male and female blastocysts had differential protein abundances, indicating differences in metabolic pathway activity. Therefore, embryos that took longer to reach the blastocyst stage of development appeared to have an imbalance between energy production and biosynthetic activity, which could differentially impact male and female embryos.

Indexed as

BlastocystEmbryonic DevelopmentProteomeAnimalsCattleEmbryo, MammalianFemaleMaleOxygen ConsumptionProteomeanabolicbiosynthesisblastocystbovinecatabolicdelayedembryometabolismmitochondriaoxidativeproteome

Identifiers

PMID40114299
PMCPMC12191644

What OpenQuestion holds

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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.