Evidence map›Paper›PMID 32470979›Full record

ArticleThe Journal of nutrition2020

Dietary Cyanidin-3-Glucoside Attenuates High-Fat-Diet-Induced Body-Weight Gain and Impairment of Glucose Tolerance in Mice via Effects on the Hepatic Hormone FGF21.

Lili Tian, Hongmei Ning, Weijuan Shao, Zhuolun Song, Yasaman Badakhshi, Wenhua Ling, Burton B Yang, Patricia L Brubaker, Tianru Jin

Open access · greenAbstract read
In one paragraph

Article in The Journal of nutrition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Hepatic hormone FGF21 and its analogues in clinical trials.Chronic diseases and translational medicine · 2022
    Review
  11. Article
  12. Article
  13. Cornelian Cherry (Nutrients · 2021
    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

9 authors at 3 institutions in 2 countries.

Lili TianDivision of Advanced Diagnostics, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
Hongmei NingDivision of Advanced Diagnostics, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
Weijuan ShaoDivision of Advanced Diagnostics, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
Zhuolun SongDivision of Advanced Diagnostics, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
Yasaman BadakhshiDivision of Advanced Diagnostics, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
Wenhua LingDepartment of Nutrition, School of Public Health, Sun Yet-Sen University, Guangzhou, China.
Burton B YangDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Patricia L BrubakerDepartment of Physiology, University of Toronto, Toronto, Canada.
Tianru JinDivision of Advanced Diagnostics, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
University Health Network · CAUniversity of Toronto · CASun Yat-sen University · CN

Funding

CIHR PJT159735
6 · The paper itself

Abstract

backgroundDietary polyphenols including anthocyanins target multiple organs.

objectiveWe aimed to assess the involvement of glucagon-like peptide 1 (GLP-1), leptin, insulin and fibroblast growth factor 21 (FGF21) in mediating metabolic beneficial effects of purified anthocyanin cyanidin-3-glucoside (Cy3G).

methodsIntestinal proglucagon gene (Gcg; encoding GLP-1) and liver Fgf21 expression were assessed in 6-wk-old male C57BL-6J mice fed a low-fat-diet (LFD; 10% of energy from fat), alone or with 1.6 mg Cy3G/L in drinking water for 3 wk [experiment (Exp.) 1; n = 5/group]. Similar mice were fed the LFD or a high-fat diet (HFD; 60% energy from fat) with or without Cy3G for 20 wk. Half of the mice administered Cy3G also received 4 broad-spectrum antibiotics (ABs) in drinking water between weeks 11 and 14, for a total of 6 groups (n = 8/group). Metabolic tolerance tests were conducted between weeks 2 and 16. Relevant hormone gene expression and plasma hormone concentrations were assessed mainly at the end of 20 wk (Exp. 2).

resultsIn Exp. 1, Cy3G administration increased ileal but not colonic Gcg level by 2-fold (P < 0.05). In Exp. 2, Cy3G attenuated HFD-induced body-weight gain (20.3% at week 16), and improved glucose tolerance (26.5% at week 15) but not insulin tolerance. Although Cy3G had no effect on glucose tolerance in LFD mice, LFD/Cy3G/AB mice showed better glucose tolerance than LFD/Cy3G mice (23%). In contrast, HFD/Cy3G/AB mice showed worse glucose tolerance compared with HFD/Cy3G mice (15%). Beneficial effects of Cy3G in HFD mice were not associated with changes in plasma leptin, insulin or GLP-1 concentrations. However, Cy3G increased hepatic Fgf21 expression in mice in Exp. 1 by 4-fold and attenuated Fgf21 overexpression in HFD mice (Exp. 2, 22%), associated with increased expression of genes that encode FGFR1 and β-klotho (>3-fold, P < 0.05).

conclusionsDietary Cy3G may reduce body weight and exert metabolic homeostatic effects in mice via changes in hepatic FGF21.

Indexed as

Glucose IntoleranceAnimalsAnthocyaninsDietary FatsDiet, High-FatFibroblast Growth FactorsGene Expression RegulationGlucagon-Like Peptide 1GlucosidesIncretinsLeptinLiverMaleMiceRandom AllocationWeight GainAnthocyaninscyanidin-3-O-beta-glucopyranosideDietary Fatsfibroblast growth factor 21Fibroblast Growth FactorsGlucagon-Like Peptide 1GlucosidesIncretinsLeptinanthocyaninCy3Gdietary interventionFGF21GLP-1OGTT

Identifiers

PMID32470979
PMCPMC7398791
OpenAlexW3032583163

What OpenQuestion holds

Textmetadata
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.