| Literature DB >> 27038926 |
Sheng-Nan Wang1,2,3, Qian Li4, Ming-Hua Jing5, Espargaró Alba6, Xiao-Hong Yang1,2,3, Raimon Sabaté6, Yi-Fan Han7, Rong-Biao Pi1,2,3,8, Wen-Jian Lan9,10,11, Xiao-Bo Yang12, Jing-Kao Chen13,14,15.
Abstract
Natural xanthones have diversity pharmacological activities. Here, a series of xanthones isolated from the pericarps of Garcinia mangostana Linn, named α-Mangostin, 8-Deoxygartanin, Gartanin, Garciniafuran, Garcinone C, Garcinone D, and γ-Mangostin were investigated. Biological screening performed in vitro and in Escherichia coli cells indicated that most of the xanthones exhibited significant inhibition of self-induced β-amyloid (Aβ) aggregation and also β-site amyloid precursor protein-cleaving enzyme 1, acted as potential antioxidants and biometal chelators. Among these compounds, α-Mangostin, Gartanin, Garcinone C and γ-Mangostin showed better antioxidant properties to scavenge Diphenyl-1-(2,4,6-trinitrophenyl) hydrazyl (DPPH) free radical than Trolox, and potent neuroprotective effects against glutamate-induced HT22 cell death partly by up-regulating HO-1 protein level and then scavenging reactive oxygen species. Moreover, Gartanin, Garcinone C and γ-Mangostin could be able to penetrate the blood-brain barrier (BBB) in vitro. These findings suggest that the natural xanthones have multifunctional activities against Alzheimer's disease (AD) and could be promising compounds for the therapy of AD.Entities:
Keywords: Alzheimer’s disease; Multifunction; Neuroprotection; Oxidative stress; Xanthones
Mesh:
Substances:
Year: 2016 PMID: 27038926 DOI: 10.1007/s11064-016-1896-y
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996