http://www.sciencedirect.com/science/article/pii/S0306452215005412
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- Icariin improved the spatial working memory of Tg2576 mice.
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- Icariin reduced the level of insoluble Aβ1-40 and Aβ1-42 and the protein expression of APP in Tg2576 mice cortex.
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- Icariin increased the adult neurogenesis in the dentate gyrus of hippocampus of Tg2576 mice.
Abstract
Icariin is a major component derived from the traditional Chinese herb Epimedium brevicornum
Maxim. Our previous studies have shown that icariin protects neurons
from the neurotoxicity and ischemia-conditions. In this study, we
investigated the effect of icariin on the expression of amyloid
precursor protein (APP) and the level of amyloid-β peptide (Aβ), as well
as neurogenesis in the brain of Tg2576 mice, an animal model of
Alzheimer’s disease (AD). Tg2576 mice and wild type littermates (WT)
were randomly assigned to three groups: Tg2576, Tg2576+icariin and WT
groups. At 9 months old, all mice were treated with icariin (60 mg/kg/d)
or distilled water for 3 months. The results showed that administration
with icariin for 3 months improved the spatial working memory of Tg2576
mice as examined in Y-maze task. Furthermore, icariin treatment reduced
the level of insoluble Aβ1-40 (69%) and Aβ1-42
(50%) in the cortex and hippocampus as determined by ELISA. Western blot
analysis indicated the down-regulation of the APP expression, and
double staining showed the elevation of BrdU/NeuN double-positive cells
in the dentate gyrus region of hippocampus compared with Tg2576 mice.
The current study demonstrated that icariin improved memory function,
decreased the levels of Aβ and APP in the brain and increased the
neurogenesis in the hippocampus of Tg2576 mice. Taken together, these
results suggest that icariin could be a potential drug candidate for AD
treatment.
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