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Original Research Article | OPEN ACCESS

Effect of carbamazepine in pentylenetetrazole-induced epilepsy in rat model

Zainab Ismail Abdul Ameer Al-Mosawi1, Reyadh H Al-Mosawi1, Mufeed Jalil Ewadh2

1Department of Pharmacology and Toxicology, College of Medicine,; 2Department of Biochemistry, College of Medicine, University of Babylon, Iraq.

For correspondence:-  Zainab Ismail Al-Mosawi   Email:

Received: 12 May 2026        Accepted: 22 July 2026        Published: 31 July 2026

Citation: Al-Mosawi ZA, Al-Mosawi RH, Ewadh MJ. Effect of carbamazepine in pentylenetetrazole-induced epilepsy in rat model. Trop J Pharm Res 2026; 25(7):941-946 doi: https://dx.doi.org/10.4314/tjpr.v25i7.5

© 2026 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the effects of carbamazepine on oxidative stress biomarkers and seizure associated behavioral alterations in pentylenetetrazole (PTZ)-induced epilepsies. Method: A total of 15 adult male Wistar rats were randomly assigned into three groups (n = 5 in each group). Group 1 was the control group and received 0.9 % normal saline, group 2 received PTZ (40 mg/kg intraperitoneal), and group 3 received carbamazepine (CBZ; 50 mg/kg, oral gavage) 1 hour before PTZ administration for 14 days. Seizure latency, frequency, and duration were assessed. Oxidative stress biomarkers, including superoxide dismutase (SOD), glutathione (GSH), and malondialdehyde (MDA), were determined in brain homogenates using standard spectrophotometric methods. Results: Pentylenetetrazole-induced changes in all measured parameters were significant at p < 0.001. However, following carbamazepine treatment, the increases in SOD and GSH were significant at p < 0.05, whereas the improvements in seizure latency, seizure frequency, seizure duration, and MDA were significant at p < 0.001. Conclusion: The study reveals that modulating oxidative stress may play a potential role in mediating the neuroprotective effects of CBZ, suggesting a promising therapeutic target in epileptogenesis.

Keywords: Carbamazepine, Epileptogenesis, Oxidative stress biomarkers, Pentylenetetrazole-induced kindling, Seizure behavior

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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