Evidence map›Paper›PMID 35390239›Full record

ArticleArhiv za higijenu rada i toksikologiju2022

Effects of naringin and valproate interaction on liver steatosis and dyslipidaemia parameters in male C57BL6 mice.

David Jutrić, Domagoj Đikić, Almoš Boroš, Dyna Odeh, Sandra Domjanić Drozdek, Romana Gračan, Petar Dragičević, Irena Crnić, Irena Landeka Jurčević

Open access · diamondAbstract read
In one paragraph

Article in Arhiv za higijenu rada i toksikologiju, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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 2 institutions in 1 country.

David JutrićUniversity of Zagreb Faculty of Science, Zagreb, Croatia.
Domagoj ĐikićUniversity of Zagreb Faculty of Science, Zagreb, Croatia.ORCID https://orcid.org/0000-0003-0909-3488
Almoš BorošUniversity of Zagreb Faculty of Science, Zagreb, Croatia.
Dyna OdehUniversity of Zagreb Faculty of Science, Zagreb, Croatia.
Sandra Domjanić DrozdekUniversity of Applied Health Sciences, Zagreb, Croatia.
Romana GračanUniversity of Zagreb Faculty of Science, Zagreb, Croatia.
Petar DragičevićUniversity of Zagreb School of Medicine, Zagreb Croatia.
Irena CrnićUniversity of Zagreb Faculty of Food Technology and Biotechnology, Zagreb, Croatia.
Irena Landeka JurčevićUniversity of Zagreb Faculty of Food Technology and Biotechnology, Zagreb, Croatia.
University of Zagreb · HRUniversity of Applied Health Sciences · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Valproate is a common antiepileptic drug whose adverse effects include liver steatosis and dyslipidaemia. The aim of our study was to see how natural flavonoid antioxidant naringin would interact with valproate and attenuate these adverse effects. For this reason we treated male C57BL6 mice with a combination of 150 mg/kg of valproate and 25 mg/kg naringin every day for 10 days and compared their serum triglycerides, cholesterol, LDL, HDL, VLDL, and liver PPAR-alpha, PGC-1 alpha, ACOX1, Nrf2, SOD, CAT, GSH, and histological signs of steatosis. Valproate increased lipid peroxidation parameters and caused pronounced microvesicular steatosis throughout the hepatic lobule in all acinar zones, but naringin co-administration limited steatosis to the lobule periphery. In addition, it nearly restored total serum cholesterol, LDL, and triglycerides and liver ACOX1 and MDA to control levels. and upregulated PPAR-alpha and PGC-1 alpha, otherwise severely downregulated by valproate. It also increased SOD activity. All these findings suggest that naringin modulates key lipid metabolism regulators and should further be investigated in this model, either alone or combined with other lipid regulating drugs or molecules.

Indexed as

DyslipidemiasFatty LiverAnimalsCholesterol, LDLFlavanonesLiverMaleMiceMice, Inbred C57BLPPAR alphaSuperoxide DismutaseTriglyceridesValproic AcidCholesterol, LDLFlavanonesnaringinPPAR alphaSuperoxide DismutaseTriglyceridesValproic AcidACOX1cholesteroldislipidemijadyslipidaemiakolesterollipid regulating transcription factorsNrf2oksidacijski stresoxidative stressPGC-1 alfaPGC-1 alphaPPAR-alfaPPAR-alphatranskripcijski faktori za regulaciju lipida

Identifiers

PMID35390239
PMCPMC8999592
OpenAlexW4223498630

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.