Dehydroevodiamine center dot HCl Protects Against Memory Impairment and Cerebral Amyloid-beta Production in Tg2576 Mice by Acting as a beta-Secretase Inhibitor

作者：Shin Ki Young; Noh Su Jin; Park Cheol Hyoung; Jeong Yun Ha; Chang Keun A; Yoo Jakyung; Kim Hee Jin; Ha Sungji; Kim Hye Sun; Park Hyun Ju; Lee Jun Ho; Moon Cheil; Suh Yoo Hun^*

来源：CNS & Neurological Disorders-Drug Targets, 2016, 15(8): 935-944.

DOI：10.2174/1871527315666160815163723

• Alzheimer's disease
• dehydroevodiamine center dot HCl
• memory
• beta-secretase
• inhibitor

We previously demonstrated that dehydroevodiamine center dot HCl (DHED), which was purified from Evodia rutaecarpa Bentham (Rutaceae), has beneficial effects on memory impairment and neuronal damage in three disease models. To investigate the preventive action of DHED in Alzheimer's disease (AD), a progressive neurodegenerative disorder characterized by memory decline, amyloid-beta (A beta) protein-containing neuritic plaques and neurofibrillary tangles, in this study, we proposed that DHED may be therapeutically effective against the memory impairment and disease-related neurochemical changes that occur in Tg2576 (Tg) mice. DHED (0.5 mg/kg) was intraperitoneally administered to 7-month-old Tg and wild type mice for 4 months. In passive avoidance and water maze tests, DHED improved memory impairment of Tg mice after 4 months of administration. DHED also reduced cortical levels of soluble A beta 40, soluble A beta 42 and total A beta peptides in the Tg mice. Additionally, we investigated whether DHED may be a beta-secretase inhibitor that affects the production of A beta related to the formation of neuritic plaques. DHED directly inhibited beta-secretase activity in a concentrationdependent manner. The concentration required for 50 % enzyme inhibition (IC50) was 40.96 mu M, and DHED may act as a competitive inhibitor of beta-secretase. Moreover, DHED interacted strongly with BACE1 (beta-secretase 2QP8), as demonstrated in the analysis of the binding mode of DHED in the active site of human BACE1. In conclusion, DHED may exhibit therapeutic effects for AD as a beta-secretase inhibitor.

• 出版日期2016