Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi, Kodaira, Tokyo 187-8502, Japan.
Psychopharmacology (Berl). 2012 Feb;219(4):1099-109. doi: 10.1007/s00213-011-2440-z. Epub 2011 Aug 23.
L-Theanine (N-ethyl-L: -glutamine) is an amino acid uniquely found in green tea and historically considered to be a relaxing agent. It is a glutamate derivative and has an affinity for glutamatergic receptors. However, its psychotropic effects remain unclear.
To elucidate effects of L: -theanine on psychiatric disease-related behaviors in mice and its molecular basis focusing on brain-derived neurotrophic factor (BDNF) and N-methyl-D: -aspartate (NMDA) receptor.
We examined the effects of L: -theanine on behaviors in mice by using the open-field test (OFT), forced swim test (FST), elevated plus-maze test (EPMT), and prepulse inhibition (PPI) of acoustic startle. By western blot analysis, we looked at the effect of L: -theanine on the expression of BDNF and related proteins in the hippocampus and cerebral cortex. To determine whether L: -theanine has agonistic action on the NMDA receptor, we performed Fluo-3 intracellular Ca(2+) imaging in cultured cortical neurons.
Single administration of L: -theanine significantly attenuated MK-801-induced deficits in PPI. Subchronic administration (3-week duration) of L: -theanine significantly reduced immobility time in the FST and improved baseline PPI. Western blotting analysis showed increased expression of BDNF protein in the hippocampus after subchronic administration of L: -theanine. In cultured cortical neurons, L: -theanine significantly increased the intracellular Ca(2+) concentration, and this increase was suppressed by competitive and non-competitive NMDA receptor antagonists (AP-5 and MK-801, respectively).
Our results suggest that L: -theanine has antipsychotic-like and possibly antidepressant-like effects. It exerts these effects, at least in part, through induction of BDNF in the hippocampus and the agonistic action of L: -theanine on the NMDA receptor.
L-茶氨酸(N-乙基-L-谷氨酰胺)是一种仅存在于绿茶中的氨基酸,历史上被认为是一种放松剂。它是谷氨酸的衍生物,对谷氨酸能受体具有亲和力。然而,其精神活性作用仍不清楚。
阐明 L-茶氨酸对小鼠精神病相关行为的影响及其分子基础,重点关注脑源性神经营养因子(BDNF)和 N-甲基-D-天冬氨酸(NMDA)受体。
我们通过使用旷场试验(OFT)、强迫游泳试验(FST)、高架十字迷宫试验(EPMT)和听觉惊跳反射的前脉冲抑制(PPI)来检查 L-茶氨酸对小鼠行为的影响。通过 Western blot 分析,我们观察了 L-茶氨酸对海马体和大脑皮层中 BDNF 及相关蛋白表达的影响。为了确定 L-茶氨酸是否对 NMDA 受体具有激动作用,我们在培养的皮质神经元中进行了 Fluo-3 细胞内 Ca(2+)成像。
单次给予 L-茶氨酸可显著减轻 MK-801 引起的 PPI 缺陷。亚慢性(3 周持续时间)给予 L-茶氨酸可显著减少 FST 中的不动时间,并改善基础 PPI。Western blot 分析显示,亚慢性给予 L-茶氨酸后海马体中 BDNF 蛋白表达增加。在培养的皮质神经元中,L-茶氨酸可显著增加细胞内 Ca(2+)浓度,而这种增加被竞争性和非竞争性 NMDA 受体拮抗剂(AP-5 和 MK-801)抑制。
我们的结果表明,L-茶氨酸具有抗精神病和可能的抗抑郁样作用。它通过在海马体中诱导 BDNF 并通过 L-茶氨酸对 NMDA 受体的激动作用发挥这些作用,至少部分如此。