Protective Effect of Oleuropein on Memory Impairment and Oxidative Stress in Streptozotocin-Induced Diabetes Rats via Modulation of NF-kB and Nrf-2 Pathways

• Hauptverfasser: Zahra Shaibani (VerfasserIn), Maryam Rafieirad (VerfasserIn)
• Format: Buch
• Veröffentlicht: Fasa University of Medical Sciences, 2024-03-01T00:00:00Z.
• Schlagworte: article
• Online-Zugang: Connect to this object online.
• Notes: 2783-1523
• Keywords: ‎diabetes; oleuropein; oxidative stress; memory; nrf-2; rat; Public aspects of medicine; RA1-1270
• Source: Journal of Advanced Biomedical Sciences, Vol 14, Iss 2, Pp 115-127 (2024)

Background & Objectives: Diabetes is the most common metabolic disease, associated with hyperglycemia and long-term complications. This study aimed to elucidate the anti-diabetic role of oleuropein (OLE) in a streptozotocin (STZ)-induced diabetic animal model. Materials & Methods: Adult male Wistar rats (200-250 g) were randomly divided into four groups: 1) Control group, 2) STZ group: diabetic rats that received STZ (60 mg/kg), 3) OLE 50 group: diabetic rats treated with oral OLE at 50 mg/kg of body weight daily for 28 days, and 4) OLE 100 group: diabetic rats treated with oral OLE at 100 mg/kg of body weight daily for 28 days. Memory function and biochemical factors such as malondialdehyde (MDA) levels, glutathione peroxidase (GPx), and total thiol activity were evaluated in the rats' cerebral cortex and striatum tissues. Moreover, nuclear transcription factor-kappa B (NF-κB) and nuclear factor E2-related factor 2 (Nrf2) pathway activation were determined in cerebral cortex and striatum tissues by real-time polymerase chain reaction (PCR). Results: Chronic administration of OLE ameliorated cognitive deficits and attenuated oxidative stress induced by diabetes. Additionally, OLE significantly prevented the activation of the pro-inflammatory marker NF-κB and downregulated Nrf2 expression in STZ-induced diabetic rats. Conclusion: Our results confirm the significant protective role of OLE against STZ-induced diabetes in rats by up-regulating Nrf2 signaling and enhancing antioxidant activity.