Abstract
The components of the herb Magnolia officinalis have exhibited antioxidant and neuroprotective activities. In this study, we investigated effects of ethanol extract of M. officinalis and its major component 4- O-methylhonokiol on memory dysfunction and neuronal cell damages caused by Aβ. Oral pretreatment of ethanol extract of M. officinalis (2.5, 5 and 10 mg/kg) and 4- O-methylhonokiol (1 mg/kg) into drinking water for 5 weeks suppressed the intraventricular treatment of Aβ 1–42 (0.5 μg/mouse, i.c.v.)-induced memory impairments. In addition, 4- O-methylhonokiol prevented the Aβ 1–42-induced apoptotic cell death as well as β-secretase expression. 4- O-methylhonokiol also inhibited H 2O 2 and Aβ 1–42-induced neurotoxicity in cultured neurons as well as PC12 cells by prevention of the reactive oxygen species generation. 4- O-methylhonokiol also directly inhibited β-secretase activity and Aβ fibrilization in vitro. Thus, ethanol extract of M. officinalis may be useful for prevention of the development or progression of AD, and 4- O-methylhonokiol may be a major active component.
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