Evidence map›Paper›PMID 37242292›Full record

ArticleNutrients2023

A Metabolic Enhancer Protects against Diet-Induced Obesity and Liver Steatosis and Corrects a Pro-Atherogenic Serum Profile in Mice.

Khrystyna Platko, Paul F Lebeau, Joshua P Nederveen, Jae Hyun Byun, Melissa E MacDonald, Jacqueline M Bourgeois, Mark A Tarnopolsky, Richard C Austin

Open access · goldFull text read
In one paragraph

Article in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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 2 institutions in 1 country.

Khrystyna PlatkoDepartment of Medicine, Division of Nephrology, McMaster University, and the Research Institute of St. Joe's Hamilton, Hamilton, ON L8N 4A6, Canada.
Paul F LebeauDepartment of Medicine, Division of Nephrology, McMaster University, and the Research Institute of St. Joe's Hamilton, Hamilton, ON L8N 4A6, Canada.
Joshua P NederveenDepartment of Pediatrics, Faculty of Health Sciences, McMaster University Medical Centre (MUMC), Hamilton, ON L8N 3Z5, Canada.
Jae Hyun ByunDepartment of Medicine, Division of Nephrology, McMaster University, and the Research Institute of St. Joe's Hamilton, Hamilton, ON L8N 4A6, Canada.
Melissa E MacDonaldDepartment of Medicine, Division of Nephrology, McMaster University, and the Research Institute of St. Joe's Hamilton, Hamilton, ON L8N 4A6, Canada.
Jacqueline M BourgeoisDepartment of Pathology and Molecular Medicine, Faculty of Health Sciences, McMaster University Medical Centre (MUMC), Hamilton, ON L8N 5Z5, Canada.
Mark A TarnopolskyDepartment of Pediatrics, Faculty of Health Sciences, McMaster University Medical Centre (MUMC), Hamilton, ON L8N 3Z5, Canada.ORCID 0000-0003-0312-3746
Richard C AustinDepartment of Medicine, Division of Nephrology, McMaster University, and the Research Institute of St. Joe's Hamilton, Hamilton, ON L8N 4A6, Canada.ORCID 0000-0003-0127-0865
St. Joseph’s Healthcare Hamilton · CAMcMaster University Medical Centre · CA

Funding

CIHR 143325CIHR 173520
6 · The paper itself

Abstract

objectiveMetabolic Syndrome (MetS) affects hundreds of millions of individuals and constitutes a major cause of morbidity and mortality worldwide. Obesity is believed to be at the core of metabolic abnormalities associated with MetS, including dyslipidemia, insulin resistance, fatty liver disease and vascular dysfunction. Although previous studies demonstrate a diverse array of naturally occurring antioxidants that attenuate several manifestations of MetS, little is known about the (i) combined effect of these compounds on hepatic health and (ii) molecular mechanisms responsible for their effect.

methodsWe explored the impact of a metabolic enhancer (ME), consisting of 7 naturally occurring antioxidants and mitochondrial enhancing agents, on diet-induced obesity, hepatic steatosis and atherogenic serum profile in mice.

resultsHere we show that a diet-based ME supplementation and exercise have similar beneficial effects on adiposity and hepatic steatosis in mice. Mechanistically, ME reduced hepatic ER stress, fibrosis, apoptosis, and inflammation, thereby improving overall liver health. Furthermore, we demonstrated that ME improved HFD-induced pro-atherogenic serum profile in mice, similar to exercise. The protective effects of ME were reduced in proprotein convertase subtilisin/kexin 9 (PCSK9) knock out mice, suggesting that ME exerts it protective effect partly in a PCSK9-dependent manner.

conclusionsOur findings suggest that components of the ME have a positive, protective effect on obesity, hepatic steatosis and cardiovascular risk and that they show similar effects as exercise training.

Indexed as

Insulin ResistanceMetabolic SyndromeNon-alcoholic Fatty Liver DiseaseAnimalsAntioxidantsDiet, High-FatLiverMiceMice, Inbred C57BLObesityProprotein Convertase 9AntioxidantsPCSK9 protein, humanProprotein Convertase 9NAFLDNASHPCSK9ROS ER stress

Identifiers

PMID37242292
PMCPMC10221984
OpenAlexW4377239657

What Socratic holds

Textfull text, public
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 Socratic graph.