Evidence map›Paper›PMID 31481463›Full record

ArticleThe Journal of biological chemistry2019

Circadian rhythm-dependent induction of hepatic lipogenic gene expression in rats fed a high-sucrose diet.

Shumin Sun, Fumiaki Hanzawa, Daeun Kim, Miki Umeki, Syunsuke Nakajima, Kumiko Sakai, Saiko Ikeda, Satoshi Mochizuki, Hiroaki Oda

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 11% 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, 30 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Circadian Clock GeneBiology · 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 5 institutions in 1 country.

Shumin SunLaboratory of Nutritional Biochemistry, Nagoya University, Nagoya 464-8601, Japan.
Fumiaki HanzawaDepartment of Nutritional Science, Nagoya University of Arts and Sciences, Nisshin 470-0196, Japan.
Daeun KimLaboratory of Nutritional Biochemistry, Nagoya University, Nagoya 464-8601, Japan.
Miki UmekiFaculty of Food Science and Nutrition, Beppu University, Beppu 874-8501, Japan.
Syunsuke NakajimaLaboratory of Nutritional Biochemistry, Nagoya University, Nagoya 464-8601, Japan.
Kumiko SakaiFaculty of Medicine, Oita University, Yufu 879-5593, Japan.
Saiko IkedaDepartment of Nutritional Science, Nagoya University of Arts and Sciences, Nisshin 470-0196, Japan.
Satoshi MochizukiFaculty of Education, Oita University, Oita 870-1192, Japan.
Hiroaki OdaLaboratory of Nutritional Biochemistry, Nagoya University, Nagoya 464-8601, Japan hirooda@agr.nagoya-u.ac.jp.ORCID 0000-0001-9129-9076
Nagoya University · JPNagoya University of Arts and Sciences · JPOita University · JPBeppu University · JPNagoya University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic syndrome has become a global health challenge and was recently reported to be positively correlated with increased sucrose consumption. Mechanistic analyses of excess sucrose-induced progression of metabolic syndrome have been focused mainly on abnormal hepatic lipogenesis, and the exact contribution of excess sucrose to metabolic disorders remains controversial. Considering that carbohydrate and lipid metabolisms exhibit clear circadian rhythms, here we investigated the possible contribution of diurnal oscillations to responses of hepatic lipid metabolism to excess sucrose. We found that excess sucrose dose-dependently promotes fatty liver and hyperlipidemia in in rats fed a high-sucrose diet (HSD). We observed that excess sucrose enhances the oscillation amplitudes of the expression of clock genes along with the levels of hepatic lipid and carbohydrate metabolism-related mRNAs that increase lipogenesis. We did not observe similar changes in the levels of the transcription factors regulating the expression of these genes. This suggested that the excess sucrose-induced, circadian rhythm-dependent amplification of lipogenesis is post-transcriptionally regulated via the stability of metabolic gene transcripts. Of note, our findings also provide evidence that fructose causes some of the HSD-induced, circadian rhythm-dependent alterations in lipogenic gene expression. Our discovery of HSD-induced circadian rhythm-dependent alterations in lipogenesis at the post-transcriptional level may inform future studies investigating the complex relationships among sucrose uptake, circadian rhythm, and metabolic enzyme expression. Our findings could contribute to the design of chrono-nutritional interventions to prevent or manage the development of fatty liver and hyperlipidemia in sucrose-induced metabolic syndrome.

Indexed as

Circadian RhythmAnimalsDietary SucroseFatty LiverHumansLipogenesisLiverMaleMetabolic SyndromeRatsRats, WistarDietary Sucrosecircadian rhythmdyslipidemiaexcess sucrose intakefatty acid metabolismgene regulationhigh-sucrose diet (HSD)lipid metabolic disorderslipogenesismetabolic syndromenonalcoholic fatty liver diseases

Identifiers

PMID31481463
PMCPMC6802514
OpenAlexW2971793097

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.