Medical Biotechnology Laboratory, Department of Biotechnology, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.
Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Mol Neurobiol. 2017 May;54(4):3050-3061. doi: 10.1007/s12035-016-9883-5. Epub 2016 Apr 1.
Modern lifestyle and sustained stress of professional commitments in the current societal set up often disrupts the normal sleep cycle and duration which is known to lead to cognitive impairments. In the present study, we report whether leaf extract of Withania somnifera (Ashwagandha) has potential neuroprotective role in acute stress of sleep deprivation. Experiments were performed on three groups of adult Wistar rats: group 1 (vehicle treated-undisturbed sleep [VUD]), group 2 (vehicle treated-sleep deprived [VSD]), and group 3 (ASH-WEX treated-sleep deprived [WSD]). Groups 1 and 2 received single oral feeding of vehicle and group 3 received ASH-WEX orally (140 mg/kg or 1 ml/250 g of body weight) for 15 consecutive days. Immediately after this regimen, animals from group 1 were allowed undisturbed sleep (between 6 a.m. and 6 p.m.), whereas rats of groups 2 and 3 were deprived of sleep during this period. We observed that WSD rats showed significant improvement in their performance in behavioral tests as compared to VSD group. At the molecular level, VSD rats showed acute change in the expression of proteins involved in synaptic plasticity, cell survival, and apoptosis in the hippocampus region of brain, which was suppressed by ASH-WEX treatment thus indicating decreased cellular stress and apoptosis in WSD group. This data suggest that Ashwagandha may be a potential agent to suppress the acute effects of sleep loss on learning and memory impairments and may emerge as a novel supplement to control SD-induced cognitive impairments.
现代生活方式和当前社会环境中持续的职业压力常常扰乱正常的睡眠周期和时长,已知这会导致认知障碍。在本研究中,我们报告了印度萝芙木(睡茄)的叶提取物是否具有在睡眠剥夺的急性应激中发挥潜在神经保护作用。实验在三组成年 Wistar 大鼠上进行:第 1 组(给予载体-未干扰睡眠[VUD])、第 2 组(给予载体-睡眠剥夺[VSD])和第 3 组(给予 ASH-WEX-睡眠剥夺[WSD])。第 1 组和第 2 组接受单次口服载体给药,第 3 组接受 ASH-WEX 口服(140mg/kg 或 1ml/250g 体重)连续 15 天。在此方案之后,第 1 组的动物被允许不受干扰地睡眠(上午 6 点至下午 6 点),而第 2 组和第 3 组的大鼠在此期间被剥夺睡眠。我们观察到,与 VSD 组相比,WSD 大鼠在行为测试中的表现有了显著改善。在分子水平上,VSD 大鼠的海马区参与突触可塑性、细胞存活和细胞凋亡的蛋白质表达发生了急性变化,而 ASH-WEX 处理抑制了这种变化,表明 WSD 组的细胞应激和细胞凋亡减少。这些数据表明,睡茄可能是一种抑制睡眠不足对学习和记忆障碍的急性影响的潜在药物,并且可能成为控制 SD 引起的认知障碍的新型补充剂。