Anatabine lowers Alzheimer's A beta production in vitro and in vivo

作者:Paris Daniel*; Beaulieu Abdelahad David; Bachmeier Corbin; Reed Jon; Ait Ghezala Ghania; Bishop Alex; Chao Jin; Mathura Venkat; Crawford Fiona; Mullan Michael
来源:European Journal of Pharmacology, 2011, 670(2-3): 384-391.
DOI:10.1016/j.ejphar.2011.09.019

摘要

Brain A beta accumulation represents a key pathological hallmark in Alzheimer's disease. In this study, we investigated the impact of anatabine, a minor alkaloid present in plants of the Solanacea family on A beta production in vitro using a cell line overexpressing the human amyloid precursor protein (APP) and in vivo using a transgenic mouse model of Alzheimer's disease. In vitro, anatabine lowers A beta(1-40) and A beta(1-42) levels in a dose dependent manner and reduces sAPP beta production without impacting sAPP alpha levels suggesting that anatabine lowers A beta production by mainly impacting the beta-cleavage of APP. Additionally, we show that anatabine lowers NF kappa B activation at doses that inhibit A beta production in vitro. Since NF kappa B is known to regulate BACE-1 expression (the rate limiting enzyme responsible for A beta production), we determined the impact of anatabine on BACE-1 transcription. We show that anatabine inhibits BACE-1 transcription and reduces BACE-1 protein levels in human neuronal like SHSY-5Y cells suggesting that the A beta lowering properties of anatabine are mediated via a regulation of BACE-1 expression. In vivo, we show that an acute treatment with anatabine for four days significantly lowers brain soluble A beta(1-40) and A beta(1-42) levels in a transgenic mouse model of Alzheimer's disease. Altogether our data suggest that anatabine may represent an interesting compound for regulating brain A beta accumulation.

  • 出版日期2011-11-30