Evidence map›Paper›PMID 37255765›Full record

ArticleJournal of diabetes and metabolic disorders2023

Underlying biochemical effects of intermittent fasting, exercise and honey on streptozotocin-induced liver damage in rats.

Ejime Agbonifo-Chijiokwu, Kingsley E Nwangwa, Mega O Oyovwi, Benneth Ben-Azu, Alexander O Naiho, Victor Emojevwe, Ejiro Peggy Ohwin, Azuka Prosper Ehiwarior, Evelyn Tarela Ojugbeli, Shalom Udoka Nwabuoku and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of diabetes and metabolic disorders, 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
3.2field-weighted citation impact, top 8% 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, 18 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Ejime Agbonifo-ChijiokwuDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Kingsley E NwangwaDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Mega O OyovwiDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Benneth Ben-AzuDepartment of Pharmacology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.ORCID 0000-0003-3569-3575
Alexander O NaihoDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Victor EmojevweDepartment of Physiology, University of Medical Sciences, Ondo, Ondo State Nigeria.
Ejiro Peggy OhwinDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Azuka Prosper EhiwariorDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Evelyn Tarela OjugbeliDepartment of Medical Biochemistry, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Shalom Udoka NwabuokuDepartment of Physiology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Emuesiri Goodies MokeDepartment of Pharmacology, Faculty of Basic Medical Science, College of Health Sciences, Delta State University, Abraka, Delta State Nigeria.
Bright O OghenetegaDepartment of Physiology, Faculty of Basic Medical Science, Babcock University, Illisan-Romo, Ogun State Nigeria.
Delta State University · NGBabcock University · NGUniversity of Medical Sciences, Ondo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Derangements of liver transcriptional factors and enzymes have important implications in diabetes-induced related complications. Hence, this study which consists of two experimental phases was aimed at evaluating the possible underlying molecular mechanisms of intermittent fasting (IF), exercise starvation and honey in streptozotocin (STZ)-mediated liver damage in diabetic rats. Methods: The diabetic rats were treated orally with distilled water (0.5 ml/kg), IF, starvation and honey at 1 g/kg body weight in the non-diabetic phase for four (4) weeks. After STZ injections, four (4) weeks of IF, exercise, starvation, and honey therapy were used as interventions prior to a biochemical evaluation of the liver. Results: IF and exercise greatly decreased liver transcription factor (resistin, SREBP-1c), inflammatory cytokines/enzyme (TNF-α, IL-6, IL-1ß, MPO) as well as oxidative and nitrergic stress with correspondence increased liver PPAR-γ, IL-10, SOD, CAT and GSH in diabetic rats unlike starvation and honey regimen relative to diabetic controls. Furthermore, IF and exercise significantly improved hepatic glycogen synthase and decreased glycogen phosphorylase in diabetic rats compared to the diabetic control group, but starvation and honey therapy had no such influence. IF and exercise strategically reduces STZ-induced liver metabolic disorder via through modulation of liver transcriptional factors and inhibition of pro-inflammatory cytokines, oxido-nitrergic and adipokine signaling pathway.

Indexed as

Diabetes mellitusExerciseFastingHoneyLiver cirrhosisOxidative stress

Identifiers

PMID37255765
PMCPMC10225416
OpenAlexW4313456758

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Registered trials

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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.