Ma Yuan, Ma Hong, Eun Jae Soon, Nam Sang-Yoon, Kim Yun-Bae, Hong Jin-Tae, Lee Myung-Koo, Oh Ki-Wan
Research Institute of Veterinary Medicine, Chungbuk National University, Cheongju 361-763, South Korea.
J Ethnopharmacol. 2009 Mar 18;122(2):245-50. doi: 10.1016/j.jep.2009.01.012.
This experiment was performed to investigate whether methanol extract of Longanae Arillus (MELA) has hypnotic effects and/or enhances pentobarbital-induced sleep behaviors through the GABAergic systems. MELA prolonged sleep time and reduced sleep latency induced by pentobarbital similar to muscimol, a GABAA receptors agonist. MELA also increased sleep rate and sleep time in the combined administration with pentobarbital at the sub-hypnotic dosage and showed synergic effects with muscimol in potentiating sleep onset and enhancing sleep time induced by pentobarbital. However, MELA itself did not induce sleep at higher dose which was used in this experiment. In addition, both of MELA and pentobarbital increased chloride influx in primary cultured cerebellar granule cells. MELA increased GABAA receptors gamma-subunit expression and had no effect on the expression of alpha- and beta-subunits, and glutamic acid decarboxylase (GAD) in primary cultured cerebellar granule cells, showing different expression of subunits from pentobarbital. In conclusion, MELA itself does not induce sleep, but it augments pentobarbital-induced sleep behaviors through the modification of GABAergic systems.
本实验旨在研究龙眼肉甲醇提取物(MELA)是否具有催眠作用,以及是否通过GABA能系统增强戊巴比妥诱导的睡眠行为。MELA延长了戊巴比妥诱导的睡眠时间并缩短了睡眠潜伏期,类似于GABAA受体激动剂蝇蕈醇。在与戊巴比妥亚催眠剂量联合给药时,MELA还提高了睡眠率和睡眠时间,并在增强戊巴比妥诱导的睡眠起始和延长睡眠时间方面与蝇蕈醇显示出协同作用。然而,在本实验中使用的较高剂量下,MELA本身并未诱导睡眠。此外,MELA和戊巴比妥均增加了原代培养的小脑颗粒细胞中的氯离子内流。MELA增加了原代培养的小脑颗粒细胞中GABAA受体γ亚基的表达,而对α亚基、β亚基和谷氨酸脱羧酶(GAD)的表达没有影响,显示出与戊巴比妥不同的亚基表达。总之,MELA本身不诱导睡眠,但它通过改变GABA能系统增强戊巴比妥诱导的睡眠行为。