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Gastroprotective effect of fluvoxamine and ondansetron on stress-induced gastric ulcers in mice

  • Mahardian Rahmadi EMAIL logo , Nily Su’aida , Pratiwi Yustisari , Wahyu Agung Dewaandika , Elma Oktavia Hanaratri , Mareta Rindang Andarsari , Sumarno and Toetik Aryani
Published/Copyright: June 25, 2021

Abstract

Objectives

The association between stress and gastric ulcers has been well reported. This study is divided into two parts: the first part of this study is consisted of analyzing the effect of fluvoxamine administration by intracerebroventricular (ICV) and intraperitoneal (IP) injections on stress-induced gastric ulcers. The second part investigates the effect of ondansetron in influencing the protection of the gastric mucous by giving fluvoxamine to the mice before being induced with stress.

Methods

Water immersion restraint stress (WIRS) was used to induce stress. Fluvoxamine 50 and 100 mg/kg by IP injection, fluvoxamine 9.3 µg, and 18.6 µg by ICV injection 30 min before the induction of stress. Meanwhile, single drug and in combination administered to the mice, ondansetron 3 mg/kg was given by IP at 60 min, and fluvoxamine 50, 100 mg/kg orally at 30 min before stress induction.

Results

The obtained results show fluvoxamine 50 and 100 mg/kg by IP, and fluvoxamine 18.6 µg by ICV had significantly reduced ulcer index with p<0.005, p<0.001, and p<0.005 while fluvoxamine 9.3 µg showed the insignificant result. Fluvoxamine 50 mg/kg, fluvoxamine 100 mg/kg, and ondansetron 3 mg/kg monotherapy have a significant reduction in ulcers with p<0.005, p<0.001, and p<0.05, while the combination drugs showed an insignificant reduction in ulcers.

Conclusions

Fluvoxamine with different administration routes and ondansetron monotherapy before stress reduce the occurrence of gastric ulcers, while the combination drugs did not increase the protective effect of the gastric mucosa.


Corresponding author: Mahardian Rahmadi, Department of Clinical Pharmacy, Faculty of Pharmacy, University of Airlangga, Surabaya, Indonesia, Phone: +62 81224656516, E-mail:

Funding source: Universitas Airlangga

Award Identifier / Grant number: 11/UN3/2020

Acknowledgments

Gratitude is owing to our colleagues from the Department of Clinical Pharmacy Universitas Airlangga for technical support over this study.

  1. Research funding: Universitas Airlangga international research Grant No. 11/UN3/2020.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors declare no conflict of interest.

  4. Ethical approval: All experiments were conducted at the Animal Research Laboratory of Faculty of Pharmacy, Universitas Airlangga, Surabaya, Indonesia, in accordance with the Guidelines for the Care and Use of Laboratory Animal issued by approved by by National Institutes of Health revised in 1985. The Ethics Committee of Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, Indonesia, approved the study protocol.

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Received: 2020-11-27
Accepted: 2021-02-21
Published Online: 2021-06-25

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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