期刊
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
卷 124, 期 -, 页码 434-442出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbb.2014.07.014
关键词
Madecassoside; Hydrocotyle sibthorpioides; Memory impairment; D-Galactose; NF-kappa B; ERK/p38 MAPK
资金
- National Natural Science Foundation of China [81260674, 81260505]
- Guangxi Natural Science Foundation [2013GXNSFAA019150, 2013GXNSFAA019146]
This study was designed to investigate the protective effect of madecassoside from Hydrocotyle sibthorpioides against cognitive impairment induced by D-galactose (D-gal) in mice. The result revealed that treatment with madecassoside significantly reversed D-gal-induced learning and memory impairments, as measured by the Morris water-maze test. Studies on the potential mechanisms of this action showed that madecassoside significantly reduced oxidative stress and suppress inflammatory responses via blocking NF-kappa B and ERK/p38 MAPK pathways. Moreover, madecassoside markedly attenuated the content and deposition of beta-amyloid peptide by inducing a decrease in the expression of amyloid protein precursor, beta-site amyloid cleaving enzyme-1 and cathepsin B and an increase in the levels of neprilysin and insulin-degrading enzyme. Madecassoside significantly increased the expression of synapse plasticity-related proteins in the hippocampus, such as postsynaptic density 95, long-term potentiation, N-methyl-D-aspartic acid receptors, Ca2+/calmodulin-dependent protein kinase II, NMDA receptor subunit 1, protein kinase C, protein kinase A, cAMP-response element binding protein, and brain-derived neurotrophic factor. In addition, madecassoside significantly increased the levels of acetylcholine but decreased cholinesterase activity. In conclusion, the protective effect of madecassoside against D-gal-induced cognitive impairment was mainly due to its ability to reduce oxidative damage, improve synaptic plasticity and restore cholinergic function. These findings suggest that madecassoside can be considered as a potential agent for preventing cognitive impairment. (C) 2014 Elsevier Inc All rights reserved.
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