Chu Qing-Ping, Wang Li-En, Cui Xiang-Yu, Fu Hong-Zheng, Lin Zhi-Bin, Lin Shu-Qian, Zhang Yong-He
Department of Pharmacology, Peking University, School of Basic Medical Science, 38 Xueyuan Lu, Beijing 100083, China.
Pharmacol Biochem Behav. 2007 Apr;86(4):693-8. doi: 10.1016/j.pbb.2007.02.015. Epub 2007 Feb 22.
Ganoderma lucidum has been used for the treatment of a variety of diseases. For the first time here we report a detailed study on the mechanisms and effects of G. lucidum aqueous extract (GLE) on sleep and its sedative activity. GLE showed no effects on sleep architecture in normal rats at doses of 80 and 120 mg/kg. However, GLE significantly decreased sleep latency, increased sleeping time, non-REM sleep time and light sleep time in pentobarbital-treated rats. Suppression of locomotor activity in normal mice induced by GLE was also observed. Flumazenil, a benzodiazepine receptor antagonist, at a dose of 3.5 mg/kg showed a significant antagonistic effect on the shortening in sleep latency, increase in sleeping time, non-REM sleep time or light sleep time in pentobarbital-treated rat induced by GLE. Significant effect was also observed with GLE on delta activity during non-REM sleep and flumazenil did not block this effect. In conclusion, GLE may be a herb having benzodiazepine-like hypnotic activity at least in part.
灵芝已被用于治疗多种疾病。在此我们首次报告了一项关于灵芝水提取物(GLE)对睡眠及其镇静活性的机制和作用的详细研究。在80和120 mg/kg剂量下,GLE对正常大鼠的睡眠结构没有影响。然而,GLE显著缩短了戊巴比妥处理大鼠的睡眠潜伏期,增加了睡眠时间、非快速眼动睡眠时间和浅睡眠时间。还观察到GLE对正常小鼠自发活动的抑制作用。氟马西尼,一种苯二氮䓬受体拮抗剂,在3.5 mg/kg剂量下对GLE诱导的戊巴比妥处理大鼠的睡眠潜伏期缩短、睡眠时间增加、非快速眼动睡眠时间或浅睡眠时间增加具有显著的拮抗作用。GLE对非快速眼动睡眠期间的δ活动也有显著影响,且氟马西尼并未阻断此作用。总之,GLE可能至少部分是一种具有苯二氮䓬样催眠活性的草药。