Nephrotoxicity after sub chronic misuse of gabapentin and the protective role of alpha-tocopherol, an experimental study | ||||
Zagazig Journal of Forensic Medicine and Toxicology | ||||
Article 3, Volume 22, Issue 1, January 2024, Page 33-54 PDF (1.06 MB) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/zjfm.2023.218877.1154 | ||||
View on SCiNiTO | ||||
Authors | ||||
Mohammad El-Kattan 1; Mahmoud Ahmed Khattab2; Fatma Abdel Wahab Abdel Maksoud3; Maha Emad Eldein4; Nada Abdel-raof5; Walaa Awad6; Ahmed Elshatory5 | ||||
1forensic medicine and clinical toxicology, mansoura University, Egypt | ||||
2Department of Medical Pharmacology, Faculty of Medicine, Cairo University, Cairo, Egypt. | ||||
3Department of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt | ||||
4Department of Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt. | ||||
5Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Cairo University, Cairo, Egypt. | ||||
6Clinical Pharmacy Department, Abo El-Reesh Al Mounira Hospital, Cairo University, Cairo, Egypt | ||||
Abstract | ||||
Background: In Egypt, gabapentin (GBP) misuse and abuse have been increased in the last decade after scheduling of its analogue pregabalin in 2012. Although many studies confirmed the deleterious effects of pregabalin, those of GBP are minimal. The aim of this research is to study and evaluate the nephrotoxic effects of sub chronic high dose administration of GBP and the protective effect of alpha-tocopherol. Methods: Thirty five (35) healthy male albino rats were included. They were randomly divided into; four groups: group I (15 rats) which were subdivided into group Ia (5 rats) negative control (normal diet), group Ib (5 rats) positve control (normal saline), group Ic (5 rats) positve control (Corn Oil), group II which were further subdivided into group IIa (5 rats) (GBP misuse), group IIb (5 rats) (GBP withdrawal), group ΙII (5 rats) (alpha-tocopherol) and group ΙV (5 rats) (GBP + alpha-tocopherol). All rats received the commenced drugs for 40 days. Serum levels of urea, creatinine and uric acid were measured. Kidney tissues were taken for histopathology. Results: GBP increased renal biomarkers levels, disrupted renal tissues and increased the number of degenerated cells. Alpha tocopherol treatment significantly attenuated the deleterious effects induced by GBP. Conclusions: High dose sub chronic administration of GBP was associated with nephrotoxic effects in rats. The histopathological effects were less appeared during withdrawal period. Alpha tocopherol protects against GBP induced impairment of kidney functions. | ||||
Keywords | ||||
Gabapentin; Misuse; Nephrotoxicity; alpha-tocopherol; Rats | ||||
Statistics Article View: 335 PDF Download: 398 |
||||