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Decrease in the production of beta-amyloid by berberine inhibition of the expression of beta-secretase in HEK293 cells

BACKGROUND: Berberine (BER), the major alkaloidal component of Rhizoma coptidis, has multiple pharmacological effects including inhibition of acetylcholinesterase, reduction of cholesterol and glucose levels, anti-inflammatory, neuroprotective and neurotrophic effects. It has also been demonstrated...

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Detalles Bibliográficos
Autores principales: Zhu, Feiqi, Wu, Fujun, Ma, Ying, Liu, Guangjian, Li, Zhong, Sun, Yong'an, Pei, Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253691/
https://www.ncbi.nlm.nih.gov/pubmed/22152059
http://dx.doi.org/10.1186/1471-2202-12-125
Descripción
Sumario:BACKGROUND: Berberine (BER), the major alkaloidal component of Rhizoma coptidis, has multiple pharmacological effects including inhibition of acetylcholinesterase, reduction of cholesterol and glucose levels, anti-inflammatory, neuroprotective and neurotrophic effects. It has also been demonstrated that BER can reduce the production of beta-amyloid(40/42), which plays a critical and primary role in the pathogenesis of Alzheimer's disease. However, the mechanism by which it accomplishes this remains unclear. RESULTS: Here, we report that BER could not only significantly decrease the production of beta-amyloid(40/42 )and the expression of beta-secretase (BACE), but was also able to activate the extracellular signal-regulated kinase1/2 (ERK1/2) pathway in a dose- and time-dependent manner in HEK293 cells stably transfected with APP695 containing the Swedish mutation. We also find that U0126, an antagonist of the ERK1/2 pathway, could abolish (1) the activation activity of BER on the ERK1/2 pathway and (2) the inhibition activity of BER on the production of beta-amyloid(40/42 )and the expression of BACE. CONCLUSION: Our data indicate that BER decreases the production of beta-amyloid(40/42 )by inhibiting the expression of BACE via activation of the ERK1/2 pathway.