Evidence map›Paper›PMID 37402020›Full record

ArticleMolecular and cellular biochemistry2024

Gluten worsens non-alcoholic fatty liver disease by affecting lipogenesis and fatty acid oxidation in diet-induced obese apolipoprotein E-deficient mice.

Edenil Costa Aguilar, Weslley Fernandes-Braga, Elandia Aparecida Santos, Paola Caroline Lacerda Leocádio, Luciano Dos Santos Aggum Capettini, Laura Alejandra Ariza Orellano, Paula Peixoto Campos, Virginia Soares Lemos, Fabíola Lacerda Pires Soares, Juliana Maria Navia-Pelaez and 1 more

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Article in Molecular and cellular biochemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Edenil Costa AguilarDepartment of Biochemistry and Immunology, ICB - Federal University of Minas Gerais, Caixa Postal 486, Belo Horizonte, 30161-970, Brazil. edenilaguilar@gmail.com.ORCID http://orcid.org/0000-0001-9035-8230
Weslley Fernandes-BragaDepartment of Biochemistry and Immunology, ICB - Federal University of Minas Gerais, Caixa Postal 486, Belo Horizonte, 30161-970, Brazil.
Elandia Aparecida SantosDepartment of Biochemistry and Immunology, ICB - Federal University of Minas Gerais, Caixa Postal 486, Belo Horizonte, 30161-970, Brazil.
Paola Caroline Lacerda LeocádioDepartment of Biochemistry and Immunology, ICB - Federal University of Minas Gerais, Caixa Postal 486, Belo Horizonte, 30161-970, Brazil.
Luciano Dos Santos Aggum CapettiniDepartment of Pharmacology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Laura Alejandra Ariza OrellanoDepartment of General Pathology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Paula Peixoto CamposDepartment of General Pathology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Virginia Soares LemosDepartment of Physiology and Biophysics, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Fabíola Lacerda Pires SoaresDepartment of Integrated Health Education, Federal University of Espírito Santo, Vitória, Brazil.
Juliana Maria Navia-PelaezDepartment of Pharmacology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Jacqueline I Alvarez-LeiteDepartment of Biochemistry and Immunology, ICB - Federal University of Minas Gerais, Caixa Postal 486, Belo Horizonte, 30161-970, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is closely associated with non-alcoholic fatty liver disease (NAFLD), characterized by hepatic fat accumulation and hepatocyte injury. Preclinical studies have shown exacerbated weight gain associated with an obesogenic gluten-containing diet. However, whether gluten affects obesity-induced hepatic lipid accumulation still remains unclear. We hypothesized that gluten intake could affect fatty liver development in high-fat diet (HFD)-induced obese mice. Thus, we aimed to investigate the impact of gluten intake on NAFLD in HFD-induced obese mice. Male apolipoprotein E-deficient (Apoe-/-) mice were fed with a HFD containing (GD) or not (GFD) vital wheat gluten (4.5%) for 10 weeks. Blood and liver were collected for further analysis. We found that gluten exacerbated weight gain, hepatic fat deposition, and hyperglycemia without affecting the serum lipid profile. Livers of the GD group showed a larger area of fibrosis, associated with the expression of collagen and MMP9, and higher expression of apoptosis-related factors, p53, p21, and caspase-3. The expression of lipogenic factors, such as PPARγ and Acc1, was more elevated and factors related to beta-oxidation, such as PPARα and Cpt1, were lower in the GD group compared to the GFD. Further, gluten intake induced a more significant expression of Cd36, suggesting higher uptake of free fatty acids. Finally, we found lower protein expression of PGC1α followed by lower activation of AMPK. Our data show that gluten-containing high-fat diet exacerbated NAFLD by affecting lipogenesis and fatty acid oxidation in obese Apoe-/- mice through a mechanism involving lower activation of AMPK.

Indexed as

Diet, High-FatFatty AcidsGlutensLipogenesisNon-alcoholic Fatty Liver DiseaseObesityOxidation-ReductionAnimalsApolipoproteins ELiverMaleMiceMice, Inbred C57BLMice, ObeseApoe protein, mouseApolipoproteins EFatty AcidsGlutensAMPKHigh-fat dietLipogenesisNAFLDWheat glutenβ-oxidation

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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.