Evidence map›Paper›PMID 38927040›Full record

ArticleBiomolecules2024

Reduced Insulin Resistance and Oxidative Stress in a Mouse Model of Metabolic Syndrome following Twelve Weeks of Citrus Bioflavonoid Hesperidin Supplementation: A Dose-Response Study.

Abdulsatar Jamal, Holly Brettle, Dina A Jamil, Vivian Tran, Henry Diep, Alexander Bobik, Chris van der Poel, Antony Vinh, Grant R Drummond, Colleen J Thomas and 2 more

Abstract read
In one paragraph

Article in Biomolecules, 2024. 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
–field-weighted citation impact
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.

  1. Review
  2. Review
  3. Article
  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

12 authors.

Abdulsatar JamalCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Holly BrettleCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Dina A JamilCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Vivian TranCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Henry DiepCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Alexander BobikCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Chris van der PoelCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Antony VinhCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Grant R DrummondCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Colleen J ThomasCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.ORCID 0000-0003-0457-715X
Maria JelinicCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.
Hayder A Al-AubaidyCentre for Cardiovascular Biology and Disease Research, La Trobe Institute for Molecular Science (LIMS), & Department of Microbiology, Anatomy, Physiology & Pharmacology (MAPP), La Trobe University, Bundoora, VIC 3086, Australia.ORCID 0000-0001-9564-0120

Funding

National Health and Medical Research Council (NHMRC) GNT1146314National Heart Foundation of Australia (NHF) Postdoctoral Fellowship 101943
6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a cluster of metabolic abnormalities affecting ~25% of adults and is linked to chronic diseases such as cardiovascular disease, cancer, and neurodegenerative diseases. Oxidative stress and inflammation are key drivers of MetS. Hesperidin, a citrus bioflavonoid, has demonstrated antioxidant and anti-inflammatory properties; however, its effects on MetS are not fully established. We aimed to determine the optimal dose of hesperidin required to improve oxidative stress, systemic inflammation, and glycemic control in a novel mouse model of MetS. Male 5-week-old C57BL/6 mice were fed a high-fat, high-salt, high-sugar diet (HFSS; 42% kcal fat content in food and drinking water with 0.9% saline and 10% high fructose corn syrup) for 16 weeks. After 6 weeks of HFSS, mice were randomly allocated to either the placebo group or low- (70 mg/kg/day), mid- (140 mg/kg/day), or high-dose (280 mg/kg/day) hesperidin supplementation for 12 weeks. The HFSS diet induced significant metabolic disturbances. HFSS + placebo mice gained almost twice the weight of control mice (

Indexed as

CitrusDietary SupplementsDisease Models, AnimalHesperidinInsulin ResistanceMetabolic SyndromeMice, Inbred C57BLOxidative StressAnimalsAntioxidantsBlood GlucoseDiet, High-FatDose-Response Relationship, DrugMaleMiceAntioxidantsBlood GlucoseHesperidin8-hydroxydeoxyguanosineHbA1chesperidininsulinmetabolic syndrome

Identifiers

PMID38927040
PMCPMC11201492

What OpenQuestion holds

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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.