Chanana Priyanka, Kumar Anil
Pharmacology Division, University Institute of Pharmaceutical Sciences, UGC Centre of Advanced Study, Panjab University, Chandigarh, India, Pin-160014.
Phytother Res. 2016 Apr;30(4):671-80. doi: 10.1002/ptr.5582. Epub 2016 Feb 5.
Sleep deprivation (SD) is an experience of inadequate or poor quality of sleep that may produce significant alterations in multiple neural systems. Centella asiatica (CA) is a psychoactive medicinal herb with immense therapeutic potential. The present study was designed to explore the possible nitric oxide (NO) modulatory mechanism in the neuroprotective effect of CA against SD induced anxiety like behaviour, oxidative damage and neuroinflammation. Male laca mice were sleep deprived for 72 h, and CA (150 and 300 mg/kg) was administered alone and in combination with NO modulators for 8 days, starting five days before 72-h SD exposure. Various behavioural (locomotor activity, elevated plus maze) and biochemical (lipid peroxidation, reduced glutathione, catalase, nitrite levels and superoxide dismutase activity), neuroinflammation marker (TNF-alpha) were assessed subsequently. CA (150 and 300 mg/kg) treatment for 8 days significantly improved locomotor activity, anti-anxiety like effect and attenuated oxidative damage and TNF α level as compared to sleep-deprived 72-h group. Also while the neuroprotective effect of CA was increased by NO antagonists, it was diminished by NO agonists. The present study suggests that NO modulatory mechanism could be involved in the protective effect of CA against SD-induced anxiety-like behaviour, oxidative damage and neuroinflammation in mice.
睡眠剥夺(SD)是一种睡眠不足或睡眠质量差的体验,可能会在多个神经系统中产生显著变化。积雪草(CA)是一种具有巨大治疗潜力的精神活性草药。本研究旨在探讨CA对SD诱导的焦虑样行为、氧化损伤和神经炎症的神经保护作用中可能的一氧化氮(NO)调节机制。雄性拉卡小鼠被睡眠剥夺72小时,在72小时SD暴露前5天开始,CA(150和300mg/kg)单独给药或与NO调节剂联合给药8天。随后评估各种行为(运动活动、高架十字迷宫)和生化指标(脂质过氧化、还原型谷胱甘肽、过氧化氢酶、亚硝酸盐水平和超氧化物歧化酶活性)、神经炎症标志物(TNF-α)。与睡眠剥夺72小时组相比,CA(150和300mg/kg)治疗8天显著改善了运动活动、抗焦虑样作用,并减轻了氧化损伤和TNF-α水平。此外,虽然NO拮抗剂增强了CA的神经保护作用,但NO激动剂则削弱了这种作用。本研究表明,NO调节机制可能参与了CA对小鼠SD诱导的焦虑样行为、氧化损伤和神经炎症的保护作用。