Tamaddonfard Sina, Erfanparast Amir, Tamaddonfard Esmaeal, Soltanalinejad Farhad
PhD Candidate, Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Vet Res Forum. 2024;15(1):35-41. doi: 10.30466/vrf.2023.2000166.3851. Epub 2024 Jan 15.
Neuroprotective effects for natural products are supported by several studies. In this regard, safranal, a constitute of saffron, has the potential to exert beneficial effects in neuro-logical disorders such as Parkinson's disease, epilepsy, stroke, multiple sclerosis and Alzheimer's disease. Here, we investigated the effect of safranal on penicillin-induced epileptiform activity. Also, the effects of intracerebroventricular (ICV) microinjection of AM251 as a CB1-cannabinoid receptors antagonist to clarify the possible mechanism of safranal were evaluated. Epileptiform activity was induced by intra-cortical administration of penicillin (300 IU, 1.50 μL) in urethane-anesthetized rats. Electrocorticographic recordings were used to analyze the frequency and amplitude of spike waves. Intraperitoneal injections of safranal at doses of 1.00 and 4.00 mg kg significantly reduced both the number and amplitude of spike waves. The ICV microinjection of AM251 (0.50 μg 2.00 μL) significantly increased the frequency and amplitude of spike waves. In addition, the anti-epileptic effect induced by administration of safranal at a dose of 4.00 mg kg was partially prevented by ICV microinjection of 0.50 μg 2.00 μL of AM251. The results showed anti-epileptiform activities for safranal. Central CB1 cannabinergic receptors might be involved in the anti-epileptiform activity of safranal.
多项研究证实了天然产物的神经保护作用。就此而言,藏红花醛作为藏红花的一种成分,有可能对帕金森病、癫痫、中风、多发性硬化症和阿尔茨海默病等神经系统疾病产生有益影响。在此,我们研究了藏红花醛对青霉素诱导的癫痫样活动的影响。此外,还评估了脑室内(ICV)微量注射AM251(一种CB1大麻素受体拮抗剂)以阐明藏红花醛可能的作用机制。在乌拉坦麻醉的大鼠中,通过皮层内注射青霉素(300 IU,1.50 μL)诱导癫痫样活动。使用脑电图记录来分析棘波的频率和幅度。腹腔注射剂量为1.00和4.00 mg/kg的藏红花醛可显著降低棘波的数量和幅度。脑室内微量注射AM251(0.50 μg,2.00 μL)可显著增加棘波的频率和幅度。此外,脑室内微量注射0.50 μg,2.00 μL的AM251可部分阻断4.00 mg/kg剂量藏红花醛诱导的抗癫痫作用。结果表明藏红花醛具有抗癫痫样活动。中枢CB1大麻素受体可能参与了藏红花醛的抗癫痫样活动。