Evidence map›Paper›PMID 41994917›Full record

ArticleMolecular nutrition & food research2026

Paternal Malnutrition has Organ-Specific Intergenerational Effects on Mitochondrial Function and Oxidative Stress Induced DNA Damage in Male Mouse Offspring.

Esther S Lenssen, Sonia de Assis, Alex Remels, Raquel Santana da Cruz, Frederik-Jan van Schooten, Roger W L Godschalk

Abstract read
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Article in Molecular nutrition & food research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Esther S LenssenInstitute of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht, Netherlands, The Netherlands.
Sonia de AssisDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Alex RemelsInstitute of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht, Netherlands, The Netherlands.
Raquel Santana da CruzDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Frederik-Jan van SchootenInstitute of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht, Netherlands, The Netherlands.ORCID 0000-0001-8111-8198
Roger W L GodschalkInstitute of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht, Netherlands, The Netherlands.

Funding

NIH HHS ES031611
6 · The paper itself

Abstract

Paternal pre-conceptional lifestyle may affect the offspring's levels of oxidative DNA damage. Therefore, we investigated whether paternal malnutrition affected mitochondrial function, oxidative stress, and DNA damage in lung and liver of mouse offspring at adult age. Adult male C57Bl6 mice received a control or low protein diet (LPD) and were mated with female mice reared on control diets. Offspring was kept under control feeding conditions until adult age. Compared to control, mitochondrial copy number and citrate synthase activity were higher in lung and liver of offspring whose fathers received LPD. Moreover, expression of genes involved in mitochondrial biogenesis was lower in lungs of offspring whose fathers received LPD, but no changes were observed in liver. Mitochondria may be a source of oxidative stress and indeed, levels of 8-oxo-deoxyguanosine (8-oxo-dG) were higher in lungs of offspring whose fathers received LPD. On the contrary, 8-oxo-dG levels in liver were lower in offspring whose father received LPD, which was associated with the tissue-specific expression of enzymatic antioxidants catalase, NAD(P)H: quinone oxidoreductase 1 and γ-glutamylcysteine synthetase. This study confirms that pre-conceptional paternal malnutrition can influence background levels of DNA damage and mitochondrial function in a tissue-specific manner in offspring.

Indexed as

DNA DamageMalnutritionMitochondriaOxidative Stress8-Hydroxy-2'-DeoxyguanosineAnimalsCatalaseCitrate (si)-SynthaseDeoxyguanosineDiet, Protein-RestrictedFemaleGlutamate-Cysteine LigaseLiverLungMaleMice8-Hydroxy-2'-DeoxyguanosineCatalaseCitrate (si)-SynthaseDeoxyguanosineGlutamate-Cysteine LigaseNAD(P)H Dehydrogenase (Quinone)DNA damagemitochondriaoffspringoxidative stressPaternal diet

Identifiers

PMID41994917
PMCPMC13088000

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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.