Evidence map›Paper›PMID 33924335›Full record

ArticleNutrients2021

Dietary Annatto-Extracted Tocotrienol Reduces Inflammation and Oxidative Stress, and Improves Macronutrient Metabolism in Obese Mice: A Metabolic Profiling Study.

Chwan-Li Shen, Sivapriya Ramamoorthy, Gurvinder Kaur, Jannette M Dufour, Rui Wang, Huanbiao Mo, Bruce A Watkins

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Revisiting the therapeutic potential of tocotrienol.BioFactors (Oxford, England) · 2022
    Review
  8. Scavenging ROS to Alleviate Acute Liver Injury by ZnO-NiO@COOH.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  9. Article
  10. Article
  11. 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

7 authors at 4 institutions in 1 country.

Chwan-Li ShenDepartment of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Sivapriya RamamoorthyMetabolon, Inc., Morrisville, NC 27560, USA.
Gurvinder KaurCenter of Excellence for Integrative Health, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Jannette M DufourCenter of Excellence for Integrative Health, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Rui WangDepartment of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Huanbiao MoDepartment of Nutrition, Georgia State University, Atlanta, GA 30303, USA.ORCID 0000-0001-7329-8117
Bruce A WatkinsDepartment of Nutrition, University of California at Davis, Davis, CA 95616, USA.
Texas Tech University · USGeorgia State University · USMetabolon (United States) · USUniversity of California, Davis · US

Funding

American River Nutrition ARNTexas Tech University Health Sciences Center TTUHSC
6 · The paper itself

Abstract

Obesity and its related complications are a world-wide health problem. Dietary tocotrienols (TT) have been shown to improve obesity-associated metabolic disorders, such as hypercholesterolemia, hyperglycemia, and gut dysbiosis. This study examined the hypothesis that the antioxidant capacity of TT alters metabolites of oxidative stress and improves systemic metabolism. C57BL/6J mice were fed either a high-fat diet (HFD control) or HFD supplemented with 800 mg annatto-extracted TT/kg (HFD+TT800) for 14 weeks. Sera from obese mice were examined by non-targeted metabolite analysis using UHPLC/MS. Compared to the HFD group, the HFD+TT800 group had higher levels of serum metabolites, essential amino acids (lysine and methionine), sphingomyelins, phosphatidylcholine, lysophospholipids, and vitamins (pantothenate, pyridoxamine, pyridoxal, and retinol). TT-treated mice had lowered levels of serum metabolites, dicarboxylic fatty acids, and inflammatory/oxidative stress markers (trimethylamine N-oxide, kynurenate, 12,13-DiHOME, and 13-HODE + 9-HODE) compared to the control. The results suggest that TT supplementation lowered inflammation and oxidative stress (oxidized glutathione and GSH/GSSH) and improved macronutrient metabolism (carbohydrates) in obese mice. Thus, TT actions on metabolites were beneficial in reducing obesity-associated hypercholesterolemia/hyperglycemia. The effects of a non-toxic dose of TT in mice support the potential for clinical applications in obesity and metabolic disease.

Indexed as

Dietary SupplementsAnimalsAntioxidantsBixaceaeCarotenoidsDiet, High-FatDisease Models, AnimalHumansInflammationMaleMiceMice, Inbred C57BLNutrientsObesityOxidative StressPlant ExtractsannattoAntioxidantsCarotenoidsNutrientsPlant ExtractsTocotrienolsinflammationmetabolitesmiceobesitytocotrienolvitamin E

Identifiers

PMID33924335
PMCPMC8069008
OpenAlexW3153462004

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.