Evidence map›Paper›PMID 40116872›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

D-carvone attenuates LPS-induced acute lung injury via TLR4/NF-κB and Nrf2/HO-1 signaling pathways in rats.

Nergis Ulaş, Hilal Üstündağ, Seçkin Özkanlar, Elif Erbaş, Adem Kara, Yunusemre Özkanlar

Abstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

6 authors.

Nergis UlaşDepartment of Internal Medicine, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.ORCID http://orcid.org/0000-0003-2340-6882
Hilal ÜstündağDepartment of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. hurcar@gmail.com.ORCID http://orcid.org/0000-0003-3140-0755
Seçkin ÖzkanlarDepartment of Biochemistry, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.ORCID http://orcid.org/0000-0001-7717-797X
Elif ErbaşDepartment of Histology and Embryology, Faculty of Veterinary Medicine, Atatürk University, Erzurum, Turkey.ORCID http://orcid.org/0000-0003-1750-3889
Adem KaraDepartment of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum, Turkey.ORCID http://orcid.org/0000-0002-5766-6116
Yunusemre ÖzkanlarDepartment of Internal Medicine, Faculty of Veterinary, Ondokuz Mayis University, Samsun, Turkey.ORCID http://orcid.org/0000-0002-1281-5413

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lung injury (ALI) is a severe respiratory disorder associated with high morbidity and mortality. Lipopolysaccharide (LPS) is widely used to induce ALI in animal models. D-carvone, a natural monoterpene, has been reported to possess anti-inflammatory and antioxidant properties. This study aimed to investigate the protective effects of D-carvone on LPS-induced ALI in rats. Thirty-six male rats were randomly divided into six groups (n = 6): control, D-carvone (10 mg/kg and 20 mg/kg p.o.), LPS (10 mg/kg E. coli lipopolysaccharide i.p.), and LPS + D-carvone (LPS with either 10 or 20 mg/kg D-carvone). D-carvone was administered orally once daily for 10 days. On day 10, sepsis was induced with LPS administration, and samples were collected after 6 h under deep anesthesia. LPS administration caused significant lung injury, as evidenced by increased histopathological scores, upregulation of pro-inflammatory markers (TLR4, IL-1β, TNF-α), and oxidative stress (increased MDA, decreased GSH and SOD). Treatment with D-carvone at both doses significantly attenuated these changes. D-carvone downregulated pro-inflammatory markers, upregulated anti-inflammatory (NRF2) and anti-apoptotic (Bcl-2) proteins, and reduced the levels of pro-inflammatory cytokines (IL-1β, TNF-α, IL-8) in lung tissues. In conclusion, D-carvone protects against LPS-induced ALI in rats, possibly through its anti-inflammatory and antioxidant properties. These findings suggest that D-carvone could be a potential therapeutic candidate for preventing and treating ALI.

Indexed as

Acute Lung InjuryAnti-Inflammatory AgentsCyclohexane MonoterpenesAnimalsAntioxidantsCytokinesHeme Oxygenase (Decyclizing)LipopolysaccharidesLungMaleNF-E2-Related Factor 2NF-kappa BOxidative StressRatsRats, Sprague-DawleyRats, WistarAnti-Inflammatory AgentsAntioxidantscarvoneCyclohexane MonoterpenesCytokinesHeme Oxygenase (Decyclizing)Hmox1 protein, ratLipopolysaccharidesNfe2l2 protein, ratNF-E2-Related Factor 2NF-kappa BTlr4 protein, ratToll-Like Receptor 4ApoptosisCytokinesD-carvoneInflammationLung injuryOxidative stressSepsis

Identifiers

PMID40116872
PMCPMC12449407

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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.