Kubota Kaori, Fukue Haruka, Sato Hitomi, Hashimoto Kana, Fujikane Aya, Moriyama Hiroshi, Watanabe Takuya, Katsurabayashi Shutaro, Kainuma Mosaburo, Iwasaki Katsunori
Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Institute for Aging and Brain Sciences, Fukuoka University, Fukuoka, Japan.
Front Pharmacol. 2017 Nov 21;8:850. doi: 10.3389/fphar.2017.00850. eCollection 2017.
Hachimijiogan (HJG) is a traditional herbal medicine that improves anxiety disorders in patients with dementia. In this study, we tested the hypothesis that HJG exerts neurotrophic factor-like effects to ameliorate memory impairment in Alzheimer disease (AD) model rats. First, we describe that HJG acts to induce neurite outgrowth in PC12 cells (a rat pheochromocytoma cell line) like nerve growth factor (NGF) in a concentration-dependent manner (3 μg/ml HJG, < 0.05; 10-500 μg/ml HJG, < 0.001). While six herbal constituents of HJG, Rehmannia root, Dioscorea rhizome, Rhizoma Alismatis, Poria sclerotium, Moutan bark, and Cinnamon bark, could induce neurite outgrowth effects, the effect was strongest with HJG (500 μg/ml). Second, we demonstrated that HJG-induced neurite outgrowth was blocked by an inhibitor of cAMP response element binding protein (CREB), KG-501 (10 μM, < 0.001). Moreover, HJG was observed to induce CREB phosphorylation 20-90 min after treatment (20 min, 2.50 ± 0.58-fold) and CRE-mediated transcription in cultured PC12 cells (500 μg/ml, < 0.01; 1000 μg/ml, < 0.001). These results suggest a CREB-dependent mechanism underlies the neurotrophic effects of HJG. Finally, we examined improvements of memory impairment following HJG treatment using a Morris water maze in AD model animals (CI + Aβ rats). Repeated oral administration of HJG improved memory impairment (300 mg/kg, < 0.05; 1000 mg/kg, < 0.001) and induced CREB phosphorylation within the hippocampus (1000 mg/kg, < 0.01). Together, our results suggest that HJG possesses neurotrophic effects similar to those of NGF, and can ameliorate cognitive dysfunction in a rat dementia model via CREB activation. Thus, HJG could potentially be a substitute for neurotrophic factors as a treatment for dementia.
八味地黄丸(HJG)是一种能改善痴呆患者焦虑症的传统草药。在本研究中,我们验证了HJG具有神经营养因子样作用以改善阿尔茨海默病(AD)模型大鼠记忆障碍的假说。首先,我们描述了HJG能像神经生长因子(NGF)一样以浓度依赖性方式诱导PC12细胞(一种大鼠嗜铬细胞瘤细胞系)的神经突生长(3μg/ml HJG,P<0.05;10 - 500μg/ml HJG,P<0.001)。虽然HJG的六种草药成分,地黄、山药、泽泻、茯苓、牡丹皮和肉桂皮,都能诱导神经突生长,但HJG(500μg/ml)的效果最强。其次,我们证明了HJG诱导的神经突生长被环磷酸腺苷反应元件结合蛋白(CREB)抑制剂KG - 501(10μM,P<0.001)阻断。此外,观察到HJG在处理后20 - 90分钟诱导CREB磷酸化(20分钟时,为2.50±0.58倍)以及在培养的PC12细胞中诱导CRE介导的转录(500μg/ml,P<0.01;1000μg/ml,P<0.001)。这些结果表明CREB依赖性机制是HJG神经营养作用的基础。最后,我们使用莫里斯水迷宫检测了HJG处理后AD模型动物(CI + Aβ大鼠)记忆障碍的改善情况。重复口服HJG改善了记忆障碍(300mg/kg,P<0.05;1000mg/kg,P<0.001)并诱导海马体内CREB磷酸化(1000mg/kg,P<0.01)。总之,我们的结果表明HJG具有与NGF相似的神经营养作用,并且可以通过激活CREB改善大鼠痴呆模型中的认知功能障碍。因此,HJG有可能作为痴呆治疗的神经营养因子替代品。