posted on 2015-06-26, 00:00authored byQin Zhao, Guo-Dong Chen, Xiao-Lin Feng, Yang Yu, Rong-Rong He, Xiao-Xia Li, Yan Huang, Wen-Xia Zhou, Liang-Dong Guo, Yi-Zhi Zheng, Xin-Sheng Yao, Hao Gao
Eight new viridins, nodulisporiviridins
A–H (1–8), were isolated from
the extract of an endolichenic
fungal strain Nodulisporium sp. (No. 65-17-2-1) that
was fermented with potato-dextrose broth. The structures were determined
using spectroscopic and X-ray crystallographic analysis. Nodulisporiviridins
A–D (1–4) are unique viridins
with an opened ring A. The Aβ42 aggregation inhibitory
activities of 1–8 were evaluated
using a thioflavin T (ThT) assay with epigallocatechin gallate (EGCG)
as the positive control (EGCG IC50 of 0.5 μM). Nodulisporiviridin
G (7) displayed potent inhibitory activity with an IC50 value of 1.2 μM, and the preliminary trend of activity
of these viridins as Aβ42 aggregation inhibitors
was proposed. The short-term memory assay on an Aβ transgenic
drosophila model of Alzheimer’s disease showed that all eight
compounds improved the short-term memory capacity, with potencies
close to that of the positive control (memantine).