Evidence map›Paper›PMID 31389908›Full record

ArticleMedicine and science in sports and exercise2020

Response of Liver Metabolic Pathways to Ketogenic Diet and Exercise Are Not Additive.

Tai-Yu Huang, Felicia R Goldsmith, Scott E Fuller, Jacob Simon, Heidi M Batdorf, Matthew C Scott, Nabil M Essajee, John M Brown, David H Burk, Christopher D Morrison and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Medicine and science in sports and exercise, 2020. 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
0.4field-weighted citation impact, top 36% 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

13 authors at 1 institution in 1 country.

Tai-Yu HuangSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
Felicia R GoldsmithSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
Scott E Fuller
Jacob SimonSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
Heidi M Batdorf
Matthew C ScottSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
Nabil M EssajeeSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
John M BrownSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
David H BurkCell Biology and Bioimaging Core, Pennington Biomedical Research Center, Baton Rouge, LA.
Christopher D MorrisonLaboratory of Neurosignaling, Pennington Biomedical Research Center, Baton Rouge, LA.
Susan J BurkeLaboratory of Immunogenetics, Pennington Biomedical Research Center, Baton Rouge, LA.
J Jason CollierLaboratory of Islet Biology and Inflammation, Pennington Biomedical Research Center, Baton Rouge, LA.
Robert C NolandSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA.
Pennington Biomedical Research Center · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Sujoy Ghosh · 2005 to 2026
$26.5M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Training in Botanical Approaches to Combat Metabolic SyndromeT32AT004094 · NCCIH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI BRANTLEY, PHILLIP J, STEPHENS, JACQUELINE M · 2009 to 2024
$5.7M
Training in Obesity ResearchT32DK064584 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI CORBY K MARTIN, Christopher D Morrison · 2003 to 2026
$5.3M
Defining the role of skeletal muscle peroxisomes in glucose homeostasisR01DK103860 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI NOLAND, ROBERT CHARLES · 2015 to 2019
$1.7M
NCCIH NIH HHS T32 AT004094NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK103860NIDDK NIH HHS T32 DK064584NIGMS NIH HHS P30 GM118430NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

purposeStudies suggest ketogenic diets (KD) produce favorable outcomes (health and exercise performance); however, most rodent studies have used a low-protein KD, which does not reflect the normal- to high-protein KD used by humans. Liver has an important role in ketoadaptation due to its involvement in gluconeogenesis and ketogenesis. This study was designed to test the hypothesis that exercise training (ExTr) while consuming a normal-protein KD (NPKD) would induce additive/synergistic responses in liver metabolic pathways.

methodsLean, healthy male C57BL/6J mice were fed a low-fat control diet (15.9% kcal protein, 11.9% kcal fat, 72.2% kcal carbohydrate) or carbohydrate-deficient NPKD (16.1% protein, 83.9% kcal fat) for 6 wk. After 3 wk on the diet, half were subjected to 3-wk treadmill ExTr (5 d·wk, 60 min·d, moderate-vigorous intensity). Upon conclusion, metabolic and endocrine outcomes related to substrate metabolism were tested in liver and pancreas.

resultsNPKD-fed mice had higher circulating β-hydroxybutyrate and maintained glucose at rest and during exercise. Liver of NPKD-fed mice had lower pyruvate utilization and greater ketogenic potential as evidenced by higher oxidative rates to catabolize lipids (mitochondrial and peroxisomal) and ketogenic amino acids (leucine). ExTr had higher expression of the gluconeogenic gene, Pck1, but lower hepatic glycogen, pyruvate oxidation, incomplete fat oxidation, and total pancreas area. Interaction effects between the NPKD and ExTr were observed for intrahepatic triglycerides, as well as genes involved in gluconeogenesis, ketogenesis, mitochondrial fat oxidation, and peroxisomal markers; however, none were additive/synergistic. Rather, in each instance the interaction effects showed the NPKD and ExTr opposed each other.

conclusionsAn NPKD and an ExTr independently induce shifts in hepatic metabolic pathways, but changes do not seem to be additive/synergistic in healthy mice.

Indexed as

Diet, Ketogenic3-Hydroxybutyric AcidAMP-Activated Protein KinasesAnimalsBlood GlucoseEnergy MetabolismFatty AcidsKetonesLeucineLipid MetabolismLiverLiver GlycogenMaleMetabolic Networks and PathwaysMice, Inbred C57BLMitochondrial Dynamics3-Hydroxybutyric AcidAMP-Activated Protein KinasesBlood GlucoseFatty AcidsKetonesLeucineLiver GlycogenPancreatic HormonesPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mousePrkaa1 protein, mouseTriglycerides

Identifiers

PMID31389908
PMCPMC6910928
OpenAlexW2965864182

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.