Evidence mapPaperPMID 42460759Full record

ArticleChemistry & biodiversity2026

From Network Analysis to Functional Nutraceutical Protection: Pistacia lentiscus L. Mitigates DMBA-Induced Liver Damage Through AhR/ARNT Pathway Regulation.

Omayma Abidi, Imen Hammami, Mariem Zakraoui, Bernard Gressier, Houcine Selmi, Bruno Eto, Ouajdi Souilem

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Omayma AbidiFaculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.ORCID https://orcid.org/0000-0001-7073-0250
Imen HammamiLaboratory of Population Health, Environmental Aggressors and Alternative Therapies (LR24ES10), Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis, Tunisia.
Mariem ZakraouiFaculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Bernard GressierLaboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Pharmacy, University of Lille, Lille, France.
Houcine SelmiLaboratory of Sylvo-Pastorales Resources, Sylvo-Pastoral Institute of Tabarka, University of Jendouba, Tabarka, Tunisia.
Bruno EtoLaboratories TBC, Laboratory of Pharmacology, Pharmacokinetics, and Clinical Pharmacy, Faculty of Pharmaceutical and Biological Sciences, University of Lille, Lille, France.
Ouajdi SouilemLaboratory of Physiology and Pharmacology, National School of Veterinary Medicine, University of Manouba, Ariana, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atmospheric pollution contributes to oxidative cellular damage and metabolic disorders due to hepatic metabolism of some toxins. In this study, we evaluated the in vitro antioxidant capacity of Pistacia lentiscus extract. Furthermore, the in vivo anti-inflammatory, antioxidant, and hepatoprotective effects were explored in DMBA-mice model. We also evaluated the systems-level characterization of gene networks associated with environmental response with genes regulated by the AhR/ARNT and HIF-2α/ARNT signaling pathways. Our results proved that P. lentiscus presented a rich source of fatty acids and secondary metabolites. In vitro, it demonstrated a strong free radical scavenging capacity with antioxidant effects. In vivo, DMBA exposure altered lipid profiles and CBCC with C-RP content, induced oxidative stress, and disrupted liver and kidney function. Cotreatment with P. lentiscus corrected plasma biochemical parameters, restored the C-RP activity and CBCC levels (C-RP: 0.9 µg/dL; WBC: 15.6 × 10

Indexed as

AntioxidantsAryl Hydrocarbon Receptor Nuclear TranslocatorChemical and Drug Induced Liver InjuryDietary SupplementsPistaciaPlant ExtractsProtective AgentsReceptors, Aryl Hydrocarbon9,10-Dimethyl-1,2-benzanthraceneAnimalsLiverMaleMiceOxidative StressSignal Transduction9,10-Dimethyl-1,2-benzanthraceneAntioxidantsAryl Hydrocarbon Receptor Nuclear TranslocatorPlant ExtractsProtective AgentsReceptors, Aryl Hydrocarbon7,12‐methylbenz(a)anthraceneAhR/ARNT pathwayantioxidant potentialbioactive compoundsdietary supplementhepatoprotectiveinflammatory potentiallipid peroxidationphytotherapy

Identifiers

PMID42460759
PMCPMC13373980

What Socratic holds

Textmetadata
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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 Socratic graph.