Evidence map›Paper›PMID 32141013›Full record

ArticleInflammopharmacology2020

Appraisal of disease-modifying potential of amlodipine as an anti-arthritic agent: new indication for an old drug.

Sumera Qasim, Alamgeer, Saima Kalsoom, Muhammad Shahzad, Hafiz Muhammad Irfan, Muhammad Shoaib Zafar, Ishfaq Ali Bukhari, Fahim Vohra, Sibtain Afzal

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Inflammopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  6. ACS omega · 2024
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  8. Review
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  10. Analysis of anti-rheumatic activity ofFrontiers in pharmacology · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Sumera QasimLaboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan.
AlamgeerLaboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan. alam_yuchi@yahoo.com.ORCID http://orcid.org/0000-0003-4775-7337
Saima KalsoomSA-CIRBS International Islamic University Islamabad Pakistan, Islamabad, Pakistan.
Muhammad ShahzadDepartment of Pharmacology, University of Health Sciences, Lahore, 54600, Pakistan.
Hafiz Muhammad IrfanLaboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan.
Muhammad Shoaib ZafarDepartment of Pharmacology, University of Health Sciences, Lahore, 54600, Pakistan.
Ishfaq Ali BukhariDepartment of Pharmacology, College of Medicine, King Saud University Riyadh, Riyadh, Saudi Arabia.
Fahim VohraDepartment of Prosthetic Dental Sciences, College of Dentistry, King Saud University, Riyadh, Saudi Arabia.
Sibtain AfzalImmunology Research Center, College of Medicine, King Saud University Riyadh, Riyadh, Saudi Arabia.
King Saud University · SAUniversity of Sargodha · PKUniversity of Health Sciences Lahore · PKInternational Islamic University, Islamabad · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amlodipine, a second-generation calcium channel blocker, exhibits documented anti-inflammatory potential. Thereby, present investigation was accomplished with an aim to explore anti-arthritic potential of amlodipine, giving a second chance to an existing drug. For validation of anti-arthritic potential of amlodipine, some in vitro models comprised of bovine serum albumin- and egg albumin-induced protein denaturation along with membrane stabilization of red blood cell was being conducted. In vivo models comprised of formaldehyde-provoked acute arthritis and CFA-instigated chronic arthritic. Paw edema, arthritic index, body weight alterations, biochemical and hematological parameters, and ankle joint histological and radiographic investigations were appraised. Moreover, RT-PCR was conducted to evaluate the levels of several inflammatory markers. Molecular docking was being conducted targeting TNF-α, IL-1β and IL-6 to establish the correlation between experimental and theoretical results. Amlodipine provides significant protection against denaturation being provoked by heating egg albumin and BSA along with stabilizing membrane of red blood cell, thereby proving in vitro anti-arthritic effect. A significant (p < 0.001) reduction in paw swelling was being observed with amlodipine in case of formaldehyde-instigated arthritis especially at the dose of 20 mg/kg. In case of CFA-provoked arthritis, reduction in paw volume and arthritic score while preservation of body weight loss and normal hematological and biochemical parameters in comparison to arthritic control were being manifested by amlodipine at the dose of 20 mg/kg. Gene expression level of TNF-α, IL-6 and IL-1β was significantly reduced by amlodipine while an increase in expression level of IL-4 and IL-10 was evident in animals treated with piroxicam and amlodipine. Molecular docking analysis demonstrated strong binding interaction of amlodipine with TNF-α, IL-6 and IL-1β thus providing a good correlation between experimental and theoretical results. Thus, current study is suggestive that amlodipine exhibits strong anti-arthritic potential and thus can be considered as a candidate for drug repurposing as anti-arthritic agent.

Indexed as

AlbuminsAmlodipineAnimalsAntirheumatic AgentsArthritis, ExperimentalCytokinesDrug RepositioningErythrocytesFemaleGene ExpressionHumansMaleRatsAlbuminsAmlodipineAntirheumatic AgentsCytokinesComplete Freund’s adjuvantMolecular dockingReal-time polymerase chain reactionRheumatoid arthritis

Identifiers

PMID32141013
OpenAlexW3009438260

What OpenQuestion holds

Textmetadata
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.