SuHeXiang Wan Essential Oil Alleviates Amyloid Beta Induced Memory Impairment Through Inhibition of Tau Protein Phosphorylation in Mice

海马体 神经毒性 药理学 β淀粉样蛋白 精油 医学 p38丝裂原活化蛋白激酶 细胞凋亡 化学 磷酸化 内科学 毒性 生物化学 MAPK/ERK通路 疾病 色谱法
作者
Songhee Jeon,Jinyoung Hur,Ha Jin Jeong,Byung‐Soo Koo,Sok Cheon Pak
出处
期刊:The American Journal of Chinese Medicine [World Scientific]
卷期号:39 (05): 917-932 被引量:32
标识
DOI:10.1142/s0192415x11009305
摘要

SuHeXiang Wan (SHXW), a traditional Chinese medicine, has been used orally for the treatment of seizures, infantile convulsions and stroke. Previously, we reported the effects of a modified SHXW essential oil in terms of sedative effect, anticonvulsant activity and antioxidative activity. The purpose of this study was to evaluate the potential beneficial effects of SHXW essential oil in neurodegenerative diseases such as Alzheimer's disease (AD). SHXW essential oil was extracted from nine herbs. The mouse AD model was induced by a single injection of amyloid β protein (Aβ 1-42 ) into the hippocampus. The animals were divided into four groups, the negative control group injected with Aβ 42-1 , the Aβ group injected with Aβ 1-42 , the SHXW group inhaled SHXW essential oil and received Aβ 1-42 injection, and the positive control group administered with docosahexaenoic acid (DHA, 10 mg/kg) and with subsequent Aβ 1-42 injection. Mice were analyzed by behavioral tests and immunological examination in the hippocampus. An additional in vitro investigation was performed to examine whether SHXW essential oil inhibits Aβ 1-42 induced neurotoxicity in a human neuroblastoma cell line, SH-SY5Y cells. Pre-inhalation of SHXW essential oil improved the Aβ 1-42 induced memory impairment and suppressed Aβ 1-42 induced JNK, p38 and Tau phosphorylation in the hippocampus. SHXW essential oil suppressed Aβ-induced apoptosis and ROS production via an up-regulation of HO-1 and Nrf2 expression in SH-SY5Y cells. The present study suggests that SHXW essential oil may have potential as a therapeutic inhalation drug for the prevention and treatment of AD.
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