Department of Pharmacology, Peking University, School of Basic Medical Science, Beijing, China.
J Ethnopharmacol. 2012 Feb 15;139(3):796-800. doi: 10.1016/j.jep.2011.12.020. Epub 2011 Dec 21.
Ganoderma lucidum (Ling Zhi) is a basidiomycete white-rot macrofungus that has been used as a tranquilizing agent (i.e., An-Shen effect) for the treatment of restlessness, insomnia, and palpitation in China for hundreds of years.
The present study aimed to investigate whether Ganoderma lucidum extract (GLE) influences the sleep of freely moving rats and the potential mechanism.
Ganoderma lucidum extract was extracted from fruiting bodies of Ganoderma lucidum. Rats were treated with GLE orally for 3 days, and on the third day, electroencephalographic and electromyographic recordings were made for 6h from 9:00 p.m. to 3:00 a.m. in freely moving rats. Sleep parameters were analyzed using SleepSign software. Tumor necrosis factor-α (TNF-α) levels were measured using the enzyme-linked immunosorbent assay.
Three-day administration of GLE significantly increased total sleep time and non-rapid eye movement (NREM) sleep time at a dose of 80 mg/kg (i.g.) without influencing slow-wave sleep or REM sleep in freely moving rats. TNF-α levels were significantly increased concomitantly in serum, the hypothalamus, and dorsal raphe nucleus. The hypnotic effect of GLE (80 mg/kg, i.g.) was significantly inhibited by intracerebroventricular injection of TNF-α antibody (2.5 μg/rat). Co-administration of GLE (40 mg/kg, i.g.) and TNF-α (12.5 ng/rat, i.c.v.), both at ineffective doses, revealed an additive hypnotic effect.
These results suggest that GLE has hypnotic effects in freely moving rats. The mechanism by which the extract promoted sleep remains unclear, but this effect appears to be primarily related to the modulation of cytokines such as TNF-α. Furthermore, these data at least partially support the ethnomedical use of Ganoderma lucidum.
灵芝(Lingzhi)是一种担子菌白腐真菌,在中国已被用作镇静剂(即安神作用),用于治疗烦躁不安、失眠和心悸已有数百年的历史。
本研究旨在探讨灵芝提取物(GLE)是否影响自由活动大鼠的睡眠及其潜在机制。
灵芝提取物从灵芝子实体中提取。大鼠连续 3 天口服 GLE,第 3 天,在自由活动大鼠中从晚上 9 点到凌晨 3 点进行 6 小时的脑电图和肌电图记录。使用 SleepSign 软件分析睡眠参数。使用酶联免疫吸附测定法测量肿瘤坏死因子-α(TNF-α)水平。
连续 3 天给予 GLE 可显著增加 80mg/kg(ig)剂量时的总睡眠时间和非快速眼动(NREM)睡眠时间,而不影响自由活动大鼠的慢波睡眠或 REM 睡眠。同时,血清、下丘脑和背侧中缝核中的 TNF-α水平也显著升高。GLE(80mg/kg,ig)的催眠作用被 TNF-α 抗体(2.5μg/大鼠,侧脑室注射)显著抑制。GLE(40mg/kg,ig)和 TNF-α(12.5ng/rat,icv)的联合给药,两者均为无效剂量,显示出相加的催眠作用。
这些结果表明,GLE 对自由活动大鼠具有催眠作用。提取物促进睡眠的机制尚不清楚,但这种作用似乎主要与细胞因子如 TNF-α的调节有关。此外,这些数据至少部分支持灵芝的民族医学用途。