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ArticleCurrent medicinal chemistry2026

Diuretic and Anti-hyperuricemic Effects of Geranyl Acetate in Rats.

Sarmad Nawaz Shah, Waqas Younis, Arquimedes Gasparotto Junior, Wajiha Manzoor, Muhammad Nasir Hayat Malik, Muhammad Naveed Mushtaq, Muhammad Usman Munir, Asifa Bashir, Shabana Bibi, Muhammad Talha and 1 more

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Article in Current medicinal chemistry, 2026. 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

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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. Article
  2. Targeting L-arginine/NO/cGMP/KFrontiers in pharmacology · 2025
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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.

Sarmad Nawaz ShahDepartment of Pharmacology, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Waqas YounisDepartment of Pharmacology, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Arquimedes Gasparotto JuniorLaboratory of Cardiovascular Pharmacology, Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Brazil.
Wajiha ManzoorDepartment of Pharmacology, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Muhammad Nasir Hayat MalikFaculty of Pharmacy, Capital University of Science and Technology, Islamabad, Pakistan.
Muhammad Naveed MushtaqDepartment of Pharmacology, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Muhammad Usman MunirAustralian Institute for Bioengineering & Nanotechnology, The University of Queensland, Brisbane, Australia.
Asifa BashirRiphah Institute of Pharmaceutical Sciences, Riphah International Univeristy, Lahore, Pakistan.
Shabana BibiDepartment of Biosciences, Shifa Tameer-e-Millat University, Islamabad, Pakistan.
Muhammad TalhaDepartment of Pharmacology, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.
Francislaine Aparecida Dos Reis LiveroLaboratory of Cardiometabolic Pharmacology, Federal University of Paraná, Curitiba, Brazil.

Funding

Foundation for the Support of Education, Science, and Technology Development of the State of Mato Grosso do Sul (FUNDECT, Brazil) 83/013.186/2023
6 · The paper itself

Abstract

backgroundGeranyl acetate, a compound found in plant oils, has been studied for its potential effects on renal and cardiovascular ailments.

objectiveThis study aimed to investigate the diuretic and anti-hyperuricemic properties of geranyl acetate in male Wistar rats using a hyperuricemia-induced rat model.

methodsMolecular docking studies were conducted to assess geranyl acetate's interactions with various targets. In vitro studies were performed to evaluate its scavenging ability and inhibition of xanthine oxidase, urease, and acetylcholinesterase. Subsequently, we administered different doses of geranyl acetate (25, 50, and 100 mg/kg) and a reference drug (furosemide) to the rats to assess their acute and repeated dose diuretic effects over seven days. To understand the diuretic mechanism, we used inhibitors, such as LNAME, indomethacin, and atropine, prior to administering geranyl acetate. We also tested the anti-hyperuricemic potential of geranyl acetate on hyperuricemic rats.

resultsMolecular docking suggested strong binding between geranyl acetate and nitric oxide synthase. In vitro studies showed significant free radical scavenging activity and and inhibition of acetylcholinesterase, xanthine oxidase, and urease. The 100 mg/kg dose exhibited the most promising diuretic effects, with nitric oxide appearing to influence its action. Uric acid excretion increased at this dose, resembling allopurinol effects.

conclusionGeranyl acetate has demonstrated significant diuretic and anti-hyperuricemic effects, likely influenced by nitric oxide release and inhibition of enzymes, like xanthine oxidase and urease. The findings have suggested potential benefits for individuals with kidney ailments, hypertension, and gout.

Indexed as

AcetatesDiureticsHyperuricemiaAcetylcholinesteraseAnimalsMaleMolecular Docking SimulationRatsRats, WistarUreaseXanthine OxidaseAcetatesAcetylcholinesteraseDiureticsUreaseXanthine OxidaseAntioxidant activitygouthypertensionhyperuricemianatural productsnitric oxidexanthine oxidase.

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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.