Evidence map›Paper›PMID 28880217›Full record

ArticleNutrients2017

The Ameliorative Effects of a Tocotrienol-Rich Fraction on the AGE-RAGE Axis and Hypertension in High-Fat-Diet-Fed Rats with Metabolic Syndrome.

Hong Sheng Cheng, So Ha Ton, Joash Ban Lee Tan, Khalid Abdul Kadir

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
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  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. S100A4 protects mice from high-fat diet-induced obesity and inflammation.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
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  12. Review
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

4 authors at 1 institution in 1 country.

Hong Sheng ChengSchool of Science, Monash University Malaysia, Bandar Sunway, Selangor 46150, Malaysia. hong.cheng@monash.edu.ORCID 0000-0001-9745-7872
So Ha TonSchool of Science, Monash University Malaysia, Bandar Sunway, Selangor 46150, Malaysia. ton.soha2016@gmail.com.
Joash Ban Lee TanSchool of Science, Monash University Malaysia, Bandar Sunway, Selangor 46150, Malaysia. tan.ban.lee@monash.edu.
Khalid Abdul KadirSchool of Medicine and Health Sciences, Monash University Malaysia, Bandar Sunway, Selangor 46150, Malaysia. khalid.kadir@monash.edu.
Monash University Malaysia · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical value of tocotrienols is increasingly appreciated because of the unique therapeutic effects that are not shared by tocopherols. However, their effect on metabolic syndrome is not well-established. This study aimed to investigate the effects of a tocotrienol-rich fraction (TRF) from palm oil in high-fat-diet-treated rats. Male, post-weaning Sprague Dawley rats were provided high-fat (60% kcal) diet for eight weeks followed by a TRF (60 mg/kg) treatment for another four weeks. Physical, metabolic, and histological changes were compared to those on control and high-fat diets respectively. High-fat feeding for eight weeks induced all hallmarks of metabolic syndrome. The TRF reversed systolic and diastolic hypertension, hypercholesterolemia, hepatic steatosis, impaired antioxidant defense, and myeloperoxidase hyperactivity triggered by the high-fat diet. It also conferred an inhibitory effect on protein glycation to reduce glycated hemoglobin A1c and advanced glycation end products (AGE). This was accompanied by the suppression of the receptor for advanced glycation end product (RAGE) expression in the liver. The treatment effects on visceral adiposity, glycemic control, triglyceride level, as well as peroxisome proliferator-activated receptor α and γ expression were negligible. To conclude, treatment with a TRF exhibited protective effects on the cardiovascular and liver health in addition to the amelioration of plasma redox imbalance and AGE-RAGE activation. Further investigation as a therapy for metabolic syndrome is therefore worthwhile.

Indexed as

AdiposityAnimalsBody CompositionDiet, High-FatEatingEnergy IntakeGlucose Tolerance TestGlycation End Products, AdvancedHumansHypertensionMaleRandom AllocationRatsRats, Sprague-DawleyReceptor for Advanced Glycation End ProductsTocotrienolsGlycation End Products, AdvancedReceptor for Advanced Glycation End ProductsTocotrienolsadvanced glycation end productcholesterolhepatic steatosismyeloperoxidaseperoxisome proliferator-activated receptorvitamin E

Identifiers

PMID28880217
PMCPMC5622744
OpenAlexW2753508208

What OpenQuestion holds

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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.