Evidence map›Paper›PMID 39342545›Full record

ArticleInflammopharmacology2024

β-Citronellol: a potential anti-inflammatory and gastro-protective agent-mechanistic insights into its modulatory effects on COX-II, 5-LOX, eNOS, and ICAM-1 pathways through in vitro, in vivo, in silico, and network pharmacology studies.

Urooj Iqbal, Abdul Malik, Nabeela Tabassum Sial, Malik Hassan Mehmood, Shoaib Nawaz, Marios Papadakis, Dalia Fouad, Hayam Ateyya, Nermeen N Welson, Athanasios Alexiou and 1 more

Abstract read
In one paragraph

Article in Inflammopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

11 authors.

Urooj IqbalDepartment of Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan.
Abdul MalikDepartment of Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan. abdul.malik@uos.edu.pk.
Nabeela Tabassum SialDepartment of Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan.
Malik Hassan MehmoodDepartment of Pharmaceutical Sciences, Government College University Lahore, Lahore, Pakistan.
Shoaib NawazThe University of Lahore, Sargodha Campus, Sargodha, Pakistan.
Marios PapadakisDepartment of Surgery II, University Hospital Witten-Herdecke, University of Witten-Herdecke, Heusnerstrasse 40, 42283, Wuppertal, Germany. drmariospapadakis@gmail.com.ORCID http://orcid.org/0000-0002-9020-874X
Dalia FouadDepartment of Zoology, College of Science, King Saud University, PO Box 22452, 11495, Riyadh, Saudi Arabia.
Hayam AteyyaDepartment of Pharmacy Practice and Clinical Pharmacy, Faculty of Pharmacy, Future University in Egypt, Cairo, Egypt.
Nermeen N WelsonDepartment of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Beni-Suef University, Beni Suef, 62511, Egypt.
Athanasios AlexiouUniversity Centre for Research and Development, Chandigarh University, Chandigarh-Ludhiana Highway, Mohali, Punjab, India.ORCID http://orcid.org/0000-0002-2206-7236
Gaber El-Saber BatihaDepartment of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour, 22511, AlBeheira, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe current study aimed to evaluate the anti-inflammatory, anti-oxidant, and pronounced gastro-protective activities of β- Citronellol using in vitro, in vivo assays and in silico approaches.

methodsIn vitro assays, denaturation of bovine serum albumin, egg protein, and human Red Blood Cells (RBCs) membrane stabilization were performed, using Piroxicam as standard. For in vivo assessment, Histamine (0.1 ml from 1% w/v) and Formaldehyde (0.1 ml from 2% v/v) were used to mediate inflammation. In silico molecular docking and network pharmacology were employed to probe the possible target genes mediating gastroprotective effect of β-Citronellol at 25, 50, and 100 mg/kg, using indomethacin-induced (25 mg/kg i.p) gastric ulcer in rats. Moreover, Gastric tissues were evaluated for morphological, histopathological, and bio-chemical analysis of PGE

resultsβ-Citronellol prevented denaturation of proteins and RBCs membrane stabilization with maximum effect observed at 6,400 µg/mL. Citronellol decreased rat's paw edema. Network pharmacology and docking studies revealed gastro-protective potential of Citronellol possibly mediated through arachidonic acid pathways by targeting COX-I, COX-II, PGE

conclusionsThe anti-inflammatory, anti-oxidant, and gastro-protective effects of β-Citronellol against indomethacin-induced gastric ulcer model in rats through mediating COX-I, COX-II, PGE

Indexed as

Acyclic MonoterpenesAnti-Inflammatory AgentsArachidonate 5-LipoxygenaseCyclooxygenase 2Intercellular Adhesion Molecule-1Molecular Docking SimulationNetwork PharmacologyNitric Oxide Synthase Type IIIRats, WistarStomach UlcerAnimalsAntioxidantsComputer SimulationHumansIndomethacinMaleAcyclic MonoterpenesAnti-Inflammatory AgentsAntioxidantsArachidonate 5-LipoxygenaseCyclooxygenase 2IndomethacinIntercellular Adhesion Molecule-1Nitric Oxide Synthase Type IIIProtective AgentsAnti-inflammatoryGastroprotectiveIndomethacinMolecular dockingNetwork pharmacologyβ-Citronellol

Identifiers

PMID39342545
PMCPMC11550294

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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.