Evidence map›Paper›PMID 42309732›Full record

ReviewThe Journal of reproduction and development2026

Environmental influences on seminal plasma: Molecular and functional insights.

Elizabeth Torres-Arce, Hon Y Chan, Brett Nixon, Natalie A Trigg, Shanu Parameswaran, Oliver J Rando, Raffaele Teperino, David A Skerrett-Byrne, Sarah A Robertson, David J Sharkey and 1 more

Abstract readReview
In one paragraph

Review in The Journal of reproduction and development, 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

11 authors.

Elizabeth Torres-ArceCentre for Reproductive Science, School of Science, College of Engineering, Science and Environment, University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Hon Y ChanSchool of Pharmacy and Biomedical Science, College of Health and Robinson Research Institute, Adelaide University, SA 5005, Australia.
Brett NixonCentre for Reproductive Science, School of Science, College of Engineering, Science and Environment, University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Natalie A TriggCentre for Reproductive Science, School of Science, College of Engineering, Science and Environment, University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Shanu ParameswaranCentre for Reproductive Science, School of Science, College of Engineering, Science and Environment, University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Oliver J RandoDepartment of Biochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, MA 01605, USA.
Raffaele TeperinoInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
David A Skerrett-ByrneReproductive and Family Health Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia.
Sarah A RobertsonSchool of Pharmacy and Biomedical Science, College of Health and Robinson Research Institute, Adelaide University, SA 5005, Australia.
David J SharkeySchool of Pharmacy and Biomedical Science, College of Health and Robinson Research Institute, Adelaide University, SA 5005, Australia.
John E SchjenkenCentre for Reproductive Science, School of Science, College of Engineering, Science and Environment, University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seminal plasma is a pivotal regulator of reproductive success that contributes to fertility and fecundity beyond its traditionally recognized function as a vehicle for spermatozoa. Rich in soluble and extracellular vesicle-encased signaling molecules, seminal plasma influences sperm integrity and function, whilst simultaneously driving profound physiological changes in the female reproductive tract. These functions are broadly conserved across vertebrate and invertebrate species and help to optimize fertilization and create an immunological environment that supports implantation and fetal development. Perturbation of seminal plasma composition or ablation of its effects can affect fertility, the progression of pregnancy and even the long-term health of offspring. Given these far‑reaching effects, the responsiveness of seminal plasma composition to environmental exposures and influences has become an important focus of research. Studies across species using a variety of different physiological perturbations or environmental exposures have shown modification to the abundance and activities of soluble and extracellular vesicle-derived seminal plasma signaling molecules. Exposures to toxins, nutritional deficiency, metabolic disturbance, and infection-associated inflammation have each been shown to affect seminal plasma components with consequences for sperm function, female reproductive tract responses, embryo development, and offspring health. Collectively, these findings position seminal plasma, in addition to spermatozoa, as an important mediator of paternal environmental influences, offering a biological means through which males convey information on their physiological state to their mates and influence reproductive success across generations.

Indexed as

Environmental ExposureReproductionSemenAnimalsFemaleFertilityHumansMalePregnancySpermatozoaEnvironmental exposureSeminal extracellular vesiclesSeminal plasma

Identifiers

PMID42309732
PMCPMC13286725

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.