Evidence mapPaperPMID 42450318Full record

ReviewInternational journal of molecular sciences2026

The Motor Neuromuscular Axis: The Overlooked Element of Developmental Programming in Diabetes and Metabolic Syndrome.

Matheus Felipe Zazula, Stephanie Rubianne Silva Carvalhal, Djennifer T Maciel, Douglas Moritz, Hellen Yukari Ito Beirauti, Luiza Amorim, Mateus Teixeira da Rocha, Mônica Maciel, Otávio Sales, Paulo Dobgenski and 7 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

17 authors.

Matheus Felipe ZazulaLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.ORCID 0000-0002-4760-5977
Stephanie Rubianne Silva CarvalhalLaboratório de Metabolismo Celular, Departamento de Fisiologia, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Djennifer T MacielLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Douglas MoritzLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Hellen Yukari Ito BeirautiLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Luiza AmorimLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Mateus Teixeira da RochaLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.ORCID 0009-0007-2177-8275
Mônica MacielLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.ORCID 0000-0003-2103-7315
Otávio SalesLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Paulo DobgenskiLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Pedro BragaLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Tayná Nery BanckesLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Thomas HorlemLaboratório de Metabolismo Celular, Departamento de Fisiologia, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.ORCID 0009-0002-6506-0605
Heloísa Deola ConfortimLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.ORCID 0000-0003-4514-6743
Paulo Ivo Homem de Bittencourt JúniorLaboratório de Fisiologia Celular, Departamento de Fisiologia, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Porto Alegre 90035-003, Rio Grande do Sul, Brazil.ORCID 0000-0003-1907-3341
Luiz Claudio FernandesLaboratório de Metabolismo Celular, Departamento de Fisiologia, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.
Katya NaliwaikoLaboratório de Plasticidade Morfofuncional, Departamento de Biologia Celular, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Curitiba 81531-908, Paraná, Brazil.ORCID 0000-0002-7950-0483

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Developmental Origins of Health and Disease framework proposes that environmental exposures during critical periods of development can shape physiological systems and influence the risk of chronic diseases later in life, including diabetes and metabolic syndrome. Most research on metabolic programming has focused on classical metabolic organs such as the liver, pancreas, and adipose tissue. However, skeletal muscle plays a central role in systemic glucose homeostasis and metabolic flexibility, accounting for the majority of insulin-stimulated glucose uptake in the body. Because muscle metabolism is closely regulated by neural activity through the organisation of motor units, the development of the motor neuromuscular axis may represent an underexplored dimension of metabolic programming. This review examines evidence linking early-life metabolic environments to neuromuscular development and discusses how alterations in the maturation of motor neurons, neuromuscular junctions, and muscle fibre phenotype may influence long-term metabolic outcomes. Evidence from epidemiological studies, experimental models, and mechanistic research suggests that maternal metabolic disturbances, including hyperglycaemia, obesity, and systemic inflammation, can influence foetal development through metabolic and inflammatory pathways affecting both neural and muscular components of the motor system. These findings support the hypothesis that the motor neuromuscular axis may represent a structural interface linking early developmental exposures to long-term metabolic regulation and risk of metabolic syndrome.

Indexed as

Diabetes Mellitus, Type 2Metabolic SyndromeMotor NeuronsNeuromuscular JunctionAnimalsDevelopmental Origins of Health and DiseaseFemaleHumansMuscle, Skeletaldevelopmental origins of health and diseasemetabolic flexibilitymetabolic programmingneuromuscular junctionskeletal muscle metabolismtype 2 diabetes

Identifiers

PMID42450318
PMCPMC13361564

What Socratic holds

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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.