Student Research Committee, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Neurosciences Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Neurochem Res. 2021 Jun;46(6):1372-1379. doi: 10.1007/s11064-021-03271-8. Epub 2021 Feb 21.
Huntington's disease (HD) is a progressive, neurodegenerative and inherited disease and recent years have witnessed the understanding of the cellular and molecular mechanisms related to HD. Safranal, an organic compound isolated from saffron, has been reported to have anti-apoptotic, anti-inflammatory and antioxidant activity and has studied in chronic and neurodegenerative disease. Therefore, this study was aimed to investigate the effect of safranal on 3-NP induced locomotor activity and biochemical alterations in rats. To this aim, 40 male Wistar rats weighting 250-300 g were divided into 5 groups (n = 8) including sham, 3-NP group (10 mg/kg) as control and treatment groups (3-NP + safranal 0.75, 1.5 and 3 mg/kg) in two weeks duration of treatment. Behavioral/movement assessments in addition to oxidant/antioxidant markers in rat cortex and striatum were evaluated in control and treatment groups. Here, we found that safranal significantly alleviated 3-NP-induced changes of body weight, rotarod activity, number of vacuous chewing movements (VCMs), and locomotor activity. In addition, brain tissue assessments in cortex and striatum revealed that safranal could prevent the elevation of nitrite and malondialdehyde (MDA) levels as well as decrease of superoxide dismutase (SOD), catalase activity and glutathione (GSH) induced by 3-NP. In conclusion our results showed that safranal prevented the motor dysfunction induced by 3-NP in animal model of Huntington's disease. This effect might be due to its modulating effect on oxidants-antioxidant balance.
亨廷顿病(HD)是一种进行性、神经退行性和遗传性疾病,近年来人们对与 HD 相关的细胞和分子机制有了更多的了解。藏红花中的一种有机化合物藏红花醛已被报道具有抗凋亡、抗炎和抗氧化活性,并在慢性和神经退行性疾病中进行了研究。因此,本研究旨在研究藏红花醛对 3-NP 诱导的大鼠运动活动和生化改变的影响。为此,将 40 只体重 250-300g 的雄性 Wistar 大鼠分为 5 组(n=8),包括假手术组、3-NP 组(10mg/kg)作为对照组和治疗组(3-NP+藏红花醛 0.75、1.5 和 3mg/kg),治疗持续 2 周。在对照组和治疗组中评估了行为/运动评估以及大鼠皮质和纹状体中的氧化应激/抗氧化标志物。结果发现,藏红花醛显著减轻了 3-NP 诱导的体重、转棒活动、空咀嚼运动(VCM)次数和运动活动的变化。此外,皮质和纹状体组织评估显示,藏红花醛可防止 3-NP 引起的亚硝酸盐和丙二醛(MDA)水平升高以及超氧化物歧化酶(SOD)、过氧化氢酶活性和谷胱甘肽(GSH)降低。总之,我们的结果表明,藏红花醛可预防 3-NP 在亨廷顿病动物模型中引起的运动功能障碍。这种作用可能是由于其对氧化应激-抗氧化平衡的调节作用。