Evidence map›Paper›PMID 41019354›Full record

ArticleF1000Research2025

Hepatoprotective potential of N-acetyl cysteine in rats with phenytoin induced liver injury.

Noor D Aziz, Deema Diyaa Azeez, Amal Umran Mosa, Zahraa Abed Al-Kareem, Sahar A Majeed, Fadhaa Abdulameer Ghafil

Abstract read
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Article in F1000Research, 2025. 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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Noor D AzizDepartment of Clinical Pharmacy, College of Pharmacy, University of Kerbala, Kerbala, Kerbala, Iraq.ORCID https://orcid.org/0000-0001-9795-0579
Deema Diyaa AzeezDepartment of Pharmaceutics, College of pharmacy, University of Kerbala, Kerbala, Iraq.
Amal Umran MosaDepartment of pharmacology and toxicology,, College of pharmacy, University of Kerbala, Kerbala, Iraq.
Zahraa Abed Al-KareemDepartment of pharmacology and therapeutics, Faculty of medicine, Kufa University, Kufa, Iraq.
Sahar A MajeedDepartment of pharmacology and therapeutics, Faculty of medicine, Kufa University, Kufa, Iraq.
Fadhaa Abdulameer GhafilDepartment of pharmacology and therapeutics, Faculty of medicine, Kufa University, Kufa, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Phenytoin is an anticonvulsant medication that is effective in treating various seizure disorders. It is mostly metabolized by the liver, which increases the risk of PHT-induced hepatotoxicity. Aims: This study aimed to assess the effectiveness of N-acetylcysteine (NAC) in protecting the liver from phenytoin-induced hepatotoxicity in rats. Materials and Methods: Four sets of five rats male Wistar albino rats (Rattus norvegicus) used for this study was based on their availability, well-established physiology, and long history of use in pharmacological and toxicological studies each were used for analysis. Each of the four groups received different treatments: the control group received normal saline, one group received 200 mg/kg/day of NAC, another group received 5 mg/kg/day of phenytoin, and the fourth group received 200 mg/kg/day of both phenytoin and NAC. The treatments were administered orally by gavage for 45 days. Biochemical indicators (aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), and total serum bilirubin (TSB)) were measured in serum after the animals were anaesthetized and the experiment ended. Histological analysis was performed on liver specimens. Results: Our investigation showed that phenytoin significantly elevated liver enzymes and total serum bilirubin compared to the control and NAC groups. The concurrent administration of NAC and phenytoin led to a notable reduction in these biomarkers, excluding ALP levels. Moreover, the group that received NAC alone did not exhibit a significant increase in the levels of these biomarkers compared with the control group. The histopathological results were in agreement with the biochemical tests. Conclusion: This study concluded that Concomitant administration of NAC and phenytoin lowered the risk of phenytoin-induced hepatotoxicity. Moreover, this study confirmed that NAC is relatively safe when administered for a relatively prolonged period.

Indexed as

AcetylcysteineChemical and Drug Induced Liver InjuryLiverPhenytoinProtective AgentsAlanine TransaminaseAnimalsAnticonvulsantsAspartate AminotransferasesBilirubinMaleRatsRats, WistarAcetylcysteineAlanine TransaminaseAnticonvulsantsAspartate AminotransferasesBilirubinPhenytoinProtective AgentsHepatoprotectiveliver injuryN-acetyl cysteinephenytoin

Identifiers

PMID41019354
PMCPMC12464531

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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.