Evidence map›Paper›PMID 38468533›Full record

ArticleCurrent pharmaceutical design2024

Repurposing of Angiotensin-converting-enzyme Inhibitor on Prevention of Post-surgical Tendon Adhesion.

Hamideh Naimi, Majid Khazaei, Fariba Sharifnia, Sayyed-Hadi Sayyed-Hosseinian

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Article in Current pharmaceutical design, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hamideh NaimiDepartment of Cellular and Molecular Biology, Islamic Azad University, North Tehran Branch, Tehran, Iran.
Majid KhazaeiMetabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Fariba SharifniaDepartment of Biology, Islamic Azad University, North Tehran Branch, Tehran, Iran.
Sayyed-Hadi Sayyed-HosseinianOrthopedic Research Center, Shahid Kamyab Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.

Funding

National Institute for Medical Research Development Grant No. 986720
6 · The paper itself

Abstract

backgroundFormation of adhesion bands is a frequent clinical complication after tendon injury or surgery with limited treatment options. This study investigates the repurposing of Angiotensin-Converting-Enzyme Inhibitor (ACEI) in attenuating post-operative tendon-sheath adhesion bands in an Achilles tendon rat model.

methodsStructural, mechanical, histological, and biochemical characteristics of the Achilles tendons were compared in the presence and absence of oral ACEI (enalapril) using the Achilles tendon adhesion (TA) model in rats. Inflammation and total fibrosis of tendon tissues were compared between groups using molecular investigations along with macroscopic and histological scoring methods.

resultsACEI significantly alleviated the severity, length, and density of Achilles TAs. Moreover, histopathological changes, recruitment of inflammatory cells, and inflammation were significantly decreased in post-operative tissue samples as quantified with the Moran scoring model. We showed that ACEI treatment elicits a potent anti-fibrotic effect on tendon tissue samples, as illustrated by decreasing the severity and extent of the formed fibrotic tissue and collagen accumulation at the site of surgery when scored either by Tang or Ishiyama grading systems. The H&E staining showed no histopathological changes or damage to the principal organs.

conclusionOur results showed that ACEI is a safe and effective therapeutic candidate with potent immunomodulatory and anti-fibrotic features to alleviate surgery-induced development of fibrotic adhesive tissue. However, its efficacy needs to be further validated in clinical studies.

Indexed as

Angiotensin-Converting Enzyme InhibitorsDrug RepositioningAchilles TendonAnimalsDisease Models, AnimalMaleRatsRats, WistarTissue AdhesionsAngiotensin-Converting Enzyme InhibitorsAchilles tendon adhesionangiotensin-converting-enzyme inhibitorenalaprilextracellular matrix.post-surgical tendon adhesionrenin-angiotensin system

Identifiers

PMID38468533

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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.