Title of article
Vitamin C Protects Against Blood and Thyroid Toxicities Induced by the Chronic Use of Carbamazepine in Rats
Author/Authors
Akorede ، Ganiu Jimoh Department of Veterinary Pharmacology and Toxicology - Faculty of Veterinary Medicine - University of Ilorin , Ambali ، Suleiman Folorunsho Department of Veterinary Pharmacology and Toxicology - Faculty of Veterinary Medicine - University of Ilorin , Olatunji ، Aisha Omobolanle Department of Veterinary Pharmacology and Toxicology - Faculty of Veterinary Medicine - University of Ilorin , Aremu ، Abdulfatai Department of Veterinary Pharmacology and Toxicology - Faculty of Veterinary Medicine - University of Ilorin , Ahmed ، Akeem Olayiwola Department of Veterinary Microbiology - Faculty of Veterinary Medicine - University of Ilorin , Basiru ، Afisu Department of Veterinary Physiology and Biochemistry - Faculty of Veterinary Medicine - University of Ilorin , Azeez ، Mistura Oyebisi Department of Veterinary Physiology and Biochemistry - Faculty of Veterinary Medicine - University of Ilorin , Sanusi ، Fatima Department of Veterinary Physiology and Biochemistry - Faculty of Veterinary Medicine - University of Ilorin , Kadir ، Rafiu Adebisi Department of Veterinary Medicine - Faculty of Veterinary Medicine - University of Ilorin , Abdulmajeed ، Isiaku Department of Veterinary Medicine - Faculty of Veterinary Medicine - University of Ilorin
From page
147
To page
156
Abstract
Background: Drugs are the mainstay of the clinical management of epilepsy. Carbamazepine (CBZ) is commonly used for treating epilepsy and neuropathic pain. This drug has been reported to have toxic effects on the hematological system due to its induction of oxidative stress. This study aimed to investigate the protective effects of vitamin C against hematological and thyroid toxicities caused by the chronic use of carbamazepine in male Wistar rats. Methods: Thirty-two adult Wistar rats were categorized randomly into four groups of eight rats each and treated as follows: Group 1 received distilled water (2 mL/kg); group 2 was treated with vitamin C (100 mg/kg); group 3 received carbamazepine (20 mg/kg), and group 4 was pre-treated with vitamin C (100 mg/kg) and given carbamazepine (20 mg/kg) 30 min later. All treatments were administered via gavage once per day over fifteen consecutive weeks. The rats’ blood samples were tested for changes in hematological parameters while the sera were evaluated for liver biochemical enzymes and thyroid hormone levels. Results: The results revealed that pre-treatment with vitamin C protected against alterations in parameters associated with hematological and thyroid toxicities. Conclusion: Based on the study results, it was concluded that: a) The chronic use of CBZ caused hematological and thyroid toxicities, and b) Vitamin C protected against these toxicities. Therefore, it is highly likely that vitamin C has the potential to protect experimental animals against injuries induced by CBZ to the liver, blood cells, and hypothalamic-pituitary-thyroid axis in a Wistar rat model.
Keywords
Blood biochemical changes , Carbamazepine , Chronic exposure , Thyrotoxicity , Vitamin C
Journal title
Iranian Journal of Toxicology
Journal title
Iranian Journal of Toxicology
Record number
2754686
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