Evidence map›Paper›PMID 31772835›Full record

ArticlePeerJ2019

Oral toxicity of arjunolic acid on hematological, biochemical and histopathological investigations in female Sprague Dawley rats.

Khurram Aamir, Hidayat Ullah Khan, Chowdhury Faiz Hossain, Mst Rejina Afrin, Imam Shaik, Naguib Salleh, Nelli Giribabu, Aditya Arya

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.8field-weighted citation impact, top 4% of its field
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

11 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. A pre-clinical study to investigate the anti-diabetic potential ofJournal of diabetes and metabolic disorders · 2023
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  7. Acute oral toxicity assessment and anti-hyperuricemic activity ofSaudi journal of biological sciences · 2022
    Article
  8. Article
  9. Article
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  11. 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

8 authors at 4 institutions in 3 countries.

Khurram AamirSchool of Pharmacy, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Malaysia.
Hidayat Ullah KhanSchool of Pharmacy, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Malaysia.
Chowdhury Faiz HossainDepartment of Pharmacy, Faculty of Science and Engineering, East West University, Dhaka, Bangladesh.ORCID 0000-0002-0218-4021
Mst Rejina AfrinDepartment of Pharmacy, Faculty of Science and Engineering, East West University, Dhaka, Bangladesh.
Imam ShaikDepartment of Pathology, School of Medicine, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Malaysia.
Naguib SallehDepartment of Physiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Nelli GiribabuDepartment of Physiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Aditya AryaDepartment of Pharmacology and Therapeutics, School of Medicine, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Malaysia.
Taylor's University · MYEast West University · BDUniversity of Malaya · MYMinistry of Science, Technology and Innovation · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundArjunolic acid (AA) is a potent phytochemical with wider pharmacological activities. Despite potential medicinal properties on various in vitro and in vivo studies, there is still a dearth of scientific data related to its safety profile and toxicological parameters. The current study aimed to investigate acute toxicity of AA in normal female Sprague Dawley rats.

methodsIn this study, AA was administered orally at an individual dose of 300 and 2000 mg/kg body weight to group 1 and 2 respectively, while group 3 served as normal control. All the animals were observed for 2 weeks to determine any behavioral and physical changes. On day 15, blood was collected for hematological and biochemical investigation, later animals from all the three groups were euthanized to harvest and store essential organs for histopathological analysis. Four different staining techniques; hematoxylin and eosin, Masson trichrome, Periodic acid Schiff and Oil O Red were used to investigate any alterations in different tissues through microscopical observation.

resultsThe results of the study showed no morbidity and mortality at two different dosage of AA treatment. Daily food & water intake, body weight, relative organ weight, hematological and biochemical parameters were detected to be normal with no severe alteration seen through microscopical investigation in the structure of harvested tissues. Our findings support the safety profile of AA, which was well tolerated at higher dose. Thus, an in-detail study on the subacute disease model is warranted.

Indexed as

Acute oral toxicityArjunolic acidBiochemical parametersBody weightFood and water intakeHematologicalHistopathologyMicroscopical investigationNo mortalityRelative organ weight

Identifiers

PMID31772835
PMCPMC6876537
OpenAlexW2990156061

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.