Samarghandian Saeed, Samini Fariborz, Azimi-Nezhad Mohsen, Farkhondeh Tahereh
Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran; Department of Neurosyrgery, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Neurosyrgery, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran; Department of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Neurosci Lett. 2017 Oct 17;659:26-32. doi: 10.1016/j.neulet.2017.08.065. Epub 2017 Sep 1.
Safranal, a major constituent of saffron, possesses antioxidant and anti-apoptotic properties showing considerable neuroprotective effects. The present study was designed to investigate the effects of safranal against restraint stress induced oxidative damage in the rat brain. For inducing the chronic restraint stress, rats were kept in the restrainers for 1h every day, for 21 consecutive days, then, the animals received systemic administrations of vehicle (0.1% DMSO) acted as the control group or safranal daily for 21days. Results indicated that the rats submitted to restraint stress showed an increase in the immobility time versus the non-stress rats. In addition, stress decreased number of crossing in the rats submitted to restraint stress versus the non-stress animals. Treatment with safranal (0.75mg/kg) showed a significant reduction in the immobility time compared to the non-treated stress group, while, the treatment improved the number of crossing in rats submitted to restraint stress versus the vehicle-treated stress rats. In the stressed animals that received vehicle, the MDA level was significantly higher and the levels of GSH and antioxidant enzymes were significantly lower than the non-stressed rats. Safranal ameliorated the changes in the stressed animals as compared with the control groups. The present findings indicate that safranal might be effective against depressant-like effects induced by chronic stress via modulating brain oxidative response.
藏红花醛是藏红花的主要成分,具有抗氧化和抗凋亡特性,显示出相当大的神经保护作用。本研究旨在探讨藏红花醛对束缚应激诱导的大鼠脑氧化损伤的影响。为诱导慢性束缚应激,将大鼠每天置于束缚器中1小时,连续21天,然后,动物接受系统给予载体(0.1%二甲基亚砜)作为对照组或每天给予藏红花醛,持续21天。结果表明,与非应激大鼠相比,遭受束缚应激的大鼠不动时间增加。此外,与非应激动物相比,应激降低了遭受束缚应激大鼠的穿越次数。与未处理的应激组相比,用藏红花醛(0.75mg/kg)处理显示不动时间显著减少,同时,与载体处理的应激大鼠相比,该处理改善了遭受束缚应激大鼠的穿越次数。在接受载体的应激动物中,丙二醛水平显著高于非应激大鼠,谷胱甘肽和抗氧化酶水平显著低于非应激大鼠。与对照组相比,藏红花醛改善了应激动物的这些变化。目前的研究结果表明,藏红花醛可能通过调节脑氧化反应有效对抗慢性应激诱导的抑郁样效应。