Evidence map›Paper›PMID 31013988›Full record

ArticleNutrients2019

A Slow-Digesting Carbohydrate Diet during Rat Pregnancy Protects Offspring from Non-Alcoholic Fatty Liver Disease Risk through the Modulation of the Carbohydrate-Response Element and Sterol Regulatory Element Binding Proteins.

Rafael Salto, Manuel Manzano, María Dolores Girón, Ainara Cano, Azucena Castro, José Dámaso Vílchez, Elena Cabrera, José María López-Pedrosa

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 11 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

8 authors at 3 institutions in 1 country.

Rafael SaltoDepartment of Biochemistry and Molecular Biology II, School of Pharmacy, University of Granada, Campus de Cartuja, 18071 Granada, Spain. rsalto@ugr.es.ORCID 0000-0002-7044-3611
Manuel ManzanoAbbott Nutrition R&D, Abbott Laboratories, 18004 Granada, Spain. manuel.manzano@abbott.com.
María Dolores GirónDepartment of Biochemistry and Molecular Biology II, School of Pharmacy, University of Granada, Campus de Cartuja, 18071 Granada, Spain. mgiron@ugr.es.ORCID 0000-0001-9638-988X
Ainara CanoOWL Metabolomics, Parque Tecnológico de Bizkaia, 48160 Deiro, Spain. acano@owlmetabolomics.com.
Azucena CastroOWL Metabolomics, Parque Tecnológico de Bizkaia, 48160 Deiro, Spain. acastro@owlmetabolomics.com.
José Dámaso VílchezDepartment of Biochemistry and Molecular Biology II, School of Pharmacy, University of Granada, Campus de Cartuja, 18071 Granada, Spain. e.damaso@go.ugr.es.ORCID 0000-0003-3256-8525
Elena CabreraDepartment of Biochemistry and Molecular Biology II, School of Pharmacy, University of Granada, Campus de Cartuja, 18071 Granada, Spain. elenacc_20@hotmail.com.
José María López-PedrosaAbbott Nutrition R&D, Abbott Laboratories, 18004 Granada, Spain. jose.m.lopez@abbott.com.
Universidad de Granada · ESAbbott (Spain) · ESEuskadiko Parke Teknologikoa · ES

Funding

European Union's Seventh Framework Programme (FP7/2007-2013) project EarlyNutrition, under grant agreement no. 289346
6 · The paper itself

Abstract

High-fat (HF) and rapid digestive (RD) carbohydrate diets during pregnancy promote excessive adipogenesis in offspring. This effect can be corrected by diets with similar glycemic loads, but low rates of carbohydrate digestion. However, the effects of these diets on metabolic programming in the livers of offspring, and the liver metabolism contributions to adipogenesis, remain to be addressed. In this study, pregnant insulin-resistant rats were fed high-fat diets with similar glycemic loads but different rates of carbohydrate digestion, High Fat-Rapid Digestive (HF-RD) diet or High Fat-Slow Digestive (HF-SD) diet. Offspring were fed a standard diet for 10 weeks, and the impact of these diets on the metabolic and signaling pathways involved in liver fat synthesis and storage of offspring were analyzed, including liver lipidomics, glycogen and carbohydrate and lipid metabolism key enzymes and signaling pathways. Livers from animals whose mothers were fed an HF-RD diet showed higher saturated triacylglycerol deposits with lower carbon numbers and double bond contents compared with the HF-SD group. Moreover, the HF-RD group exhibited enhanced glucose transporter 2, pyruvate kinase (PK), acetyl coenzyme A carboxylase (ACC) and fatty acid (FA) synthase expression, and a decrease in pyruvate carboxylase (PyC) expression leading to an altered liver lipid profile. These parameters were normalized in the HF-SD group. The changes in lipogenic enzyme expression were parallel to changes in AktPKB phosphorylation status and nuclear expression in carbohydrate-response element and sterol regulatory element binding proteins. In conclusion, an HF-RD diet during pregnancy translates to changes in liver signaling and metabolic pathways in offspring, enhancing liver lipid storage and synthesis, and therefore non-alcoholic fatty liver disease (NAFLD) risk. These changes can be corrected by feeding an HF-SD diet during pregnancy.

Indexed as

Carbohydrate MetabolismAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsDietary CarbohydratesDiet, High-FatDigestionFemaleGene Expression RegulationGlucose Transporter Type 2Non-alcoholic Fatty Liver DiseasePregnancyPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleyRisk FactorsSterol Regulatory Element Binding Protein 1Basic Helix-Loop-Helix Leucine Zipper Transcription FactorsDietary CarbohydratesGlucose Transporter Type 2Mlxipl protein, ratSlc2a2 protein, ratSrebf1 protein, ratSterol Regulatory Element Binding Protein 1Sterol Regulatory Element Binding Protein 2early programminghepatic lipogenesisinsulin-resistant pregnancymetabolic flexibilitynon-alcoholic fatty liver diseaseslow digesting carbohydrates

Identifiers

PMID31013988
PMCPMC6521114
OpenAlexW2935766557

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.