Evidence map›Paper›PMID 42524633›Full record

ArticleAnimal reproduction2026

Molecular and developmental consequences of heat stress on the bovine oocyte and embryo competence.

Ghyslaine Giselle Ramírez, Nico Graham Menjivar, Samuel Gebremedhn, Ahmed Gad, Eva Held-Hoelker, Michael Hoelker, Genet Zewdie, Dawit Tesfaye

Abstract read
In one paragraph

Article in Animal reproduction, 2026. 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

8 authors.

Ghyslaine Giselle RamírezAnimal Reproduction and Biotechnology Laboratory - ARBL, Department of Biomedical Sciences, Colorado State University, Fort Collins, CO, United States of America.ORCID 0009-0008-3098-1619
Nico Graham MenjivarStanford Fertility and Reproductive Health Services, Stanford Medicine Children's Health, Sunnyvale, CA, United States of America.ORCID 0000-0003-0853-4165
Samuel GebremedhnJ.R. Simplot Company, Boise, ID, United States of America.ORCID 0000-0002-9977-2347
Ahmed GadAnimal Reproduction and Biotechnology Laboratory - ARBL, Department of Clinical Sciences, Colorado State University, Fort Collins, CO, USA.ORCID 0000-0001-9741-2105
Eva Held-HoelkerDepartment of Animal Breeding, Institute of Animal Sciences, University of Bonn, Bonn, Germany.ORCID 0009-0006-4732-9550
Michael HoelkerDepartment of Animal Science, Biotechnology and Reproduction of Farm Animals, Georg-August-University Goettingen, Göttingen, Germany.ORCID 0000-0002-7878-6491
Genet ZewdieAddis Abeba University, Addis Abeba, Ethiopia.ORCID 0009-0000-1482-8843
Dawit TesfayeAnimal Reproduction and Biotechnology Laboratory - ARBL, Department of Biomedical Sciences, Colorado State University, Fort Collins, CO, United States of America.ORCID 0000-0001-8166-0606

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seasonal heat stress (HS) is a pervasive environmental challenge with profound consequences for female reproductive physiology, affecting ovarian function, oocyte maturation, and early embryonic development. At the ovarian level, HS disrupts follicular growth, impairs steroidogenesis, and compromises granulosa cell function, thereby creating a suboptimal microenvironment that reduces oocyte competence. In oocytes, HS induces oxidative stress, mitochondrial dysfunction, endoplasmic reticulum (ER) stress, spindle abnormalities, chromosomal missegregation, and persistent epigenetic alterations. These disruptions extend into early embryonic development, where redox imbalance, apoptosis, ER stress, and altered lineage allocation reduce cleavage and blastocyst formation, compromise trophectoderm and inner cell mass integrity, and impair implantation potential. Maternal heat exposure further exacerbates embryonic vulnerability by altering the oviductal and uterine environment, reducing embryotrophic factors and antioxidant defenses, and ultimately influencing offspring phenotype and fertility, potentially across generations. Accordingly, this review aims to synthesize current knowledge on the physiological and molecular impacts of heat stress on ovarian function, oocyte maturation, and early embryonic development. To this end, we consider studies conducted under both in vivo and in vitro conditions, highlighting shared and distinct mechanisms of thermal stress at the organ and cellular levels to identify potential targets for intervention.

Indexed as

heat stressoocyte and embryoovaryreproduction

Identifiers

PMID42524633
PMCPMC13412142

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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.