Evidence map›Paper›PMID 37362383›Full record

ArticleJournal of the Endocrine Society2023

Intermittent Fasting Sustainably Improves Glucose Tolerance in Normal Weight Male Mice Through Histone Hyperacetylation.

Sho Endo, Asuka Uto, Kazutoshi Miyashita, Masaaki Sato, Hiroyuki Inoue, Kentaro Fujii, Aika Hagiwara, Masaki Ryuzaki, Takuma Oshida, Kenichiro Kinouchi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

11 authors at 1 institution in 1 country.

Sho EndoDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Asuka UtoDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.ORCID https://orcid.org/0000-0002-1584-2345
Kazutoshi MiyashitaDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.ORCID https://orcid.org/0000-0003-3757-4334
Masaaki SatoDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Hiroyuki InoueDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Kentaro FujiiDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Aika HagiwaraDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Masaki RyuzakiDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Takuma OshidaDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Kenichiro KinouchiDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Hiroshi ItohDepartment of Internal Medicine, Keio University School of Medicine, Tokyo, 160-8582, Japan.ORCID https://orcid.org/0000-0003-2514-4919
Keio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To explore the mechanism by which intermittent fasting (IF) exerts prolonged effects after discontinuation, we examined mice that had been subjected to 4 cycles of fasting for 72 hours and ad libitum feeding for 96 hours per week (72hIF), followed by 4 weeks of ad libitum feeding, focusing on expression of genes for lipid metabolism in the skeletal muscle and histone acetylation in the promoter region. The 72hIF regimen resulted in metabolic remodeling, characterized by enhanced lipid utilization and mitochondrial activation in the muscle. This long-term IF (72hIF) caused stronger metabolic effects than alternate day fasting (24hIF) wherein fasting and refeeding are repeated every 24 hours. Upregulation of lipid oxidation genes and an increase in oxygen utilization were sustained even at 4 weeks after discontinuation of 72hIF, associated with histone hyperacetylation of the promoter region of uncoupling protein 3 (

Indexed as

exercise enduranceglucose tolerancehistone acetylationintermittent fastinglipid oxidationmitochondria

Identifiers

PMID37362383
PMCPMC10290492
OpenAlexW4381095067

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.