Evidence map›Paper›PMID 36075960›Full record

ArticleCommunications biology2022

Paternal low protein diet perturbs inter-generational metabolic homeostasis in a tissue-specific manner in mice.

Hannah L Morgan, Samuel Furse, Irundika H K Dias, Kiran Shabir, Marcos Castellanos, Iqbal Khan, Sean T May, Nadine Holmes, Matthew Carlile, Fei Sang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
19.8field-weighted citation impact, top 1% of its field
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

16 citing papers in PubMed, 44 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Hannah L MorganLifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK.
Samuel FurseCore Metabolomics and Lipidomics Laboratory, Wellcome-MRC Institute of Metabolic Science, University of Cambridge, Addenbrooke's Treatment Centre, Keith Day Road, Cambridge, CB2 0QQ, UK.ORCID http://orcid.org/0000-0003-4267-2051
Irundika H K DiasAston Medical School, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
Kiran ShabirAston Medical School, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
Marcos CastellanosNottingham Arabidopsis Stock Centre (NASC), University of Nottingham, Sutton Bonington Campus, Plant Science Building, School of Biosciences, Loughborough, LE12 5RD, UK.
Iqbal KhanNottingham Arabidopsis Stock Centre (NASC), University of Nottingham, Sutton Bonington Campus, Plant Science Building, School of Biosciences, Loughborough, LE12 5RD, UK.
Sean T MayNottingham Arabidopsis Stock Centre (NASC), University of Nottingham, Sutton Bonington Campus, Plant Science Building, School of Biosciences, Loughborough, LE12 5RD, UK.ORCID http://orcid.org/0000-0001-5282-3250
Nadine HolmesDeep Seq, School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, NG7 2UH, UK.
Matthew CarlileDeep Seq, School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, NG7 2UH, UK.ORCID http://orcid.org/0000-0002-3786-8167
Fei SangDeep Seq, School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, NG7 2UH, UK.ORCID http://orcid.org/0000-0002-8746-5868
Victoria WrightDeep Seq, School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, NG7 2UH, UK.
Albert KoulmanCore Metabolomics and Lipidomics Laboratory, Wellcome-MRC Institute of Metabolic Science, University of Cambridge, Addenbrooke's Treatment Centre, Keith Day Road, Cambridge, CB2 0QQ, UK.ORCID http://orcid.org/0000-0001-9998-051X
Adam J WatkinsLifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK. adam.watkins@nottingham.ac.uk.ORCID http://orcid.org/0000-0002-0842-1251
University of Nottingham · GBAston University · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M027252/1Biotechnology and Biological Sciences Research Council BB/R003556/1
6 · The paper itself

Abstract

The underlying mechanisms driving paternally-programmed metabolic disease in offspring remain poorly defined. We fed male C57BL/6 mice either a control normal protein diet (NPD; 18% protein) or an isocaloric low protein diet (LPD; 9% protein) for a minimum of 8 weeks. Using artificial insemination, in combination with vasectomised male mating, we generated offspring using either NPD or LPD sperm but in the presence of NPD or LPD seminal plasma. Offspring from either LPD sperm or seminal fluid display elevated body weight and tissue dyslipidaemia from just 3 weeks of age. These changes become more pronounced in adulthood, occurring in conjunction with altered hepatic metabolic and inflammatory pathway gene expression. Second generation offspring also display differential tissue lipid abundance, with profiles similar to those of first generation adults. These findings demonstrate that offspring metabolic homeostasis is perturbed in response to a suboptimal paternal diet with the effects still evident within a second generation.

Indexed as

Diet, Protein-RestrictedSemenAnimalsFathersHomeostasisHumansMaleMiceMice, Inbred C57BL

Identifiers

PMID36075960
PMCPMC9458637
OpenAlexW4294942494

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.