Discovering the Hepatoprotective Properties of ARA290 in Acetaminophen-Induced Liver Toxicity

Introduction: Erythropoietin (EPO), known for its hematopoietic function, also has anti-inflammatory, antiapoptotic, antioxidant, and cytoprotective effects. ARA290, a peptide derived from EPO, selectively interacts with the innate repair receptor and exhibits similar properties. ARA290 offers tissue protection like EPO but without the hematopoietic side effects that limit EPO’s clinical use. In vitro, bioassays are important in evaluating new agents with hepatoprotective effects. This study aimed to assess the effect of ARA290 pretreatment on acetaminophen (APAP)-induced damage in HepG2 cells.

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Publication Details

Journal
Applied In Vitro Toxicology
Published
2025-04-23
DOI
https://doi.org/10.1089/aivt.2024.0026
Citations
1
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
1.56
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article

Discovering the Hepatoprotective Properties of ARA290 in Acetaminophen-Induced Liver Toxicity

Nasrin Ghassemi-Barghi, Ramina Fazeli, Maryam Fakhri
1 citations
Applied In Vitro Toxicology
Drug-Induced Hepatotoxicity and Protection
1.56
article

Discovering the Hepatoprotective Properties of ARA290 in Acetaminophen-Induced Liver Toxicity

Nasrin Ghassemi-Barghi, Ramina Fazeli, Maryam Fakhri
article en
1 citations

Abstract

Introduction: Erythropoietin (EPO), known for its hematopoietic function, also has anti-inflammatory, antiapoptotic, antioxidant, and cytoprotective effects. ARA290, a peptide derived from EPO, selectively interacts with the innate repair receptor and exhibits similar properties. ARA290 offers tissue protection like EPO but without the hematopoietic side effects that limit EPO’s clinical use. In vitro, bioassays are important in evaluating new agents with hepatoprotective effects. This study aimed to assess the effect of ARA290 pretreatment on acetaminophen (APAP)-induced damage in HepG2 cells.

Applied In Vitro ToxicologyVol. 11(2)
University of Tehran (IR), Jahrom University of Medical Sciences (IR), Tehran University of Medical Sciences (IR)
Openalex Percentile: Top 21%
Drug-Induced Hepatotoxicity and Protection
1.56
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