Evidence map›Paper›PMID 39825436›Full record

ArticleBMC pharmacology & toxicology2025

Potential antihyperlipidemic effects of myrcenol and curzerene in high-fat fed rats.

Sana Tahir, Abdullah Abdo, Aisha Mobashar, Arham Shabbir, Komal Najam, Aisha Ibrahim, Khalid Hussain, Yousef A Bin Jardan, Samir Ibenmoussa, Youssouf Ali Younous

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

10 authors.

Sana TahirFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Abdullah AbdoFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Aisha MobasharFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan. aishamobashar@gmail.com.
Arham ShabbirDepartment of Pharmacology, Institute of Pharmacy, Faculty of Pharmaceutical and Allied Health Sciences, Lahore College for Women University, Lahore, Pakistan.
Komal NajamFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Aisha IbrahimFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Khalid HussainFaculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Yousef A Bin JardanDepartment of Pharmaceutics, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia.
Samir IbenmoussaLaboratory of Therapeutic and Organic Chemistry, Faculty of Pharmacy, University of Montpellier, Montpellier, 34000, France.
Youssouf Ali YounousEvangelical College, N'Djamena, BP 1200, Chad. scientifcresearcher@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study evaluated the anti-hyperlipidemic effects of myrcenol and curzerene on a high fat diet induced hyperlipidemia rat model. Thirty male albino rats were fed on a high-fat diet for four months. The HFD-induced hyperperlipidemia rats were treated with rosuvastatin (10 mg/kg), curzerene (130 mg/kg) and myrcenol (100 mg/kg) for four weeks. Blood samples were collected for further analysis. Aorta and heart were harvested for histopathological evaluation. Hepatic lipase and HMG-CoA reductase were determined by ELISA. FST and Y-maze tests were performed to assess the stress level in hyperlipidemia rats. The phytochemical compounds (Curzerene and Myrcenol) and the standard drug (Rosuvastatin) resulted in decreased body weight as well as reduced levels of LDL, TG, TC, AST and ALT as compared to the diseased group. Additionally, the treated groups displayed improved HDL levels and less depressed behavior. The ELISA results revealed that the Curzerene and myrcenol had significantly increased the protein concentration of hepatic lipase than the diseased group whereas both compounds significantly lowered the HMG-CoA reductase concentrations compared to the diseased group. The findings suggested that myrcenol and curzerene had the potential to be therapeutic agents for managing hyperlipidemia and reducing the risk of heart-related conditions associated with high lipid levels.

Indexed as

HyperlipidemiasHypolipidemic AgentsAnimalsAortaDiet, High-FatHydroxymethylglutaryl CoA ReductasesLipaseLiverMaleRatsHydroxymethylglutaryl CoA ReductasesHypolipidemic AgentsLipaseCurzereneHepatic lipaseHMG-Co A reductaseHyperlipidemiaMyrcenol

Identifiers

PMID39825436
PMCPMC11742224

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.