Evidence map›Paper›PMID 41137704›Full record

ArticleExperimental physiology2026

Impact of diet and exercise in growth restricted female rats on nephron endowment in male fetuses.

Jessica F Briffa, Sogand Gravina, Viktoria F Richter, Dayana Mahizir, Kristina Anevska, Yeukai T M Mangwiro, James S M Cuffe, Fadi Charchar, Glenn D Wadley, Deanne H Hryciw and 2 more

Abstract read
In one paragraph

Article in Experimental physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Jessica F BriffaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.ORCID https://orcid.org/0000-0001-5173-4790
Sogand GravinaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
Viktoria F RichterDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
Dayana MahizirDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
Kristina AnevskaDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
Yeukai T M MangwiroDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
James S M CuffeSchool of Biomedical Sciences, The University of Queensland, St. Lucia, QLD, Australia.
Fadi CharcharFaculty of Science and Technology, School of Applied and Biomedical Sciences, Federation University Australia, Ballarat, VIC, Australia.
Glenn D WadleyInstitute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Deakin University, Burwood, VIC, Australia.
Deanne H HryciwDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.
Karen M MoritzSchool of Biomedical Sciences, The University of Queensland, St. Lucia, QLD, Australia.
Mary E WlodekDepartment of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.ORCID https://orcid.org/0000-0002-8490-9099

Funding

DHAC | National Health and Medical Research Council (NHMRC) 1045602Diabetes Australia Research Trust (DART)
6 · The paper itself

Abstract

Uteroplacental insufficiency impairs kidney development and programs male-onset cardiorenal disease, which can be transmitted to subsequent generations. Maternal lifestyle factors can independently influence fetal kidney development, highlighting that the lifestyle of growth-restricted females can have further influence on F2 kidney development. In this study, we examined the impact of maternal growth restriction with or without additional lifestyle factors on F2 male kidney development. Uteroplacental insufficiency (Restricted) or sham (Control) surgery was performed on embryonic day 18 in Wistar-Kyoto rats. F1 females were fed a Chow or High-fat diet from weaning (5 weeks of age). At 16 weeks, females were randomly allocated to an exercise group: no exercise (Sedentary); exercised prior to and during pregnancy (Exercise); or exercised only during pregnancy (PregEx). Females were mated at 20 weeks, with F2 male kidneys collected (embryonic day 20). Maternal growth restriction alone reduced nephron endowment by 29%, whereas additional lifestyle factors in Restricted dams reduced nephron endowment by ∼43%. Interestingly, Exercise only in High-fat dams did not alter nephron endowment, which is likely to be attributable to significant kidney remodelling and/or enhanced resource availability. This study demonstrates that growth-restricted dams that experience multiple maternal lifestyle factors (i.e. High-fat diet and PregEx) impair the development of male F2 kidneys to a more severe extent than fetuses exposed to maternal growth restriction alone or a single maternal lifestyle factor in dams of normal birth weight (i.e. high-fat feeding or exercise alone). Importantly, positive lifestyle interventions (Exercise) in a high-fat environment compounded by adverse metabolic programming (Restriction) can be beneficial to fetal kidney development, which might prevent the transgenerational programming of cardiorenal disease.

Indexed as

Fetal Growth RetardationNephronsPhysical Conditioning, AnimalAnimalsDiet, High-FatFemaleFetal DevelopmentFetusKidneyMalePlacental InsufficiencyPregnancyRatsRats, Inbred WKYexercisegrowth restrictionhigh‐fat dietkidneynephron endowmentsecond generation

Identifiers

PMID41137704
PMCPMC12949101

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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.