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Licensed Unlicensed Requires Authentication Published by De Gruyter December 17, 2020

Concurrent administration of acetaminophen and ethanol: impact on mouse liver and testis

  • Jonah Sydney Aprioku EMAIL logo and Precious Gospel

Abstract

Objectives

Acetaminophen (paracetamol) and alcohol are widely consumed as analgesic/antipyretic and recreational agent, respectively. High doses of both agents induce liver and male reproductive toxicities. This study investigated the toxicological outcome of concurrent administration of paracetamol and ethanol in the liver and testis in mice.

Methods

Animals were gavaged paracetamol (250 mg/kg), ethanol (3 g/kg) or paracetamol + ethanol for 2 d. Some groups were sacrificed 12 h after the last dose, while others were sacrificed 21 d posttreatment for reversibility study. Control group received carboxymethylcellulose sodium (0.2%). Serum levels of liver biochemical indices and epididymal sperm were analysed. Histopathological analysis of the liver and testis were also performed.

Results

Alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and bilirubin in serum were elevated (p<0.001); whereas albumin and total protein were reduced (p<0.001) in paracetamol or ethanol groups compared to control. In the combination group, only mild elevation of ALT (p<0.05) was observed. Additionally, hepatocyte necrosis occurred in the livers of paracetamol and ethanol groups, while only mild inflammatory changes were seen in the combination group. All liver indices were normal in reversibility study animals. Furthermore, sperm count, motility, viability and morphology did not change in all treated animals, except that sperm count was decreased (p<0.05) in paracetamol group. Testis histology of all animal groups were normal.

Conclusions

The results demonstrated that simultaneous treatment with acute paracetamol and ethanol doses will possibly minimize hepatotoxicity and reduction of epididymal sperm reserve by the individual agents, and the toxicities are reversible.


Corresponding author: Jonah Sydney Aprioku, Department of Experimental Pharmacology and Toxicology, Faculty of Pharmaceutical Sciences, University of Port Harcourt, East-West Road, Choba, Port Harcourt, Rivers, PMB 5323, Nigeria, Phone: +234(0) 8035082379, E-mail:

Acknowledgments

We are grateful to the laboratory staff of the Department of Experimental Pharmacology and Toxicology, University of Port Harcourt, Nigeria for providing technical support during the animal studies.

  1. Research funding: Research did not receive any external funding.

  2. Author contributions: JSA conceived and designed the study. GP managed the literature searches, and contribute in conduction of the experiments and collection of data. JSA handled the analysis of the data, wrote the protocol and the first draft of the manuscript. Both authors approved the final manuscript.

  3. Competing interests: Authors have no conflict of interest to report.

  4. Ethical approval: All experimental procedures were approved by the Research Ethics Committee of the University of Port Harcourt, Nigeria.

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Received: 2020-05-20
Accepted: 2020-08-29
Published Online: 2020-12-17

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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