Pratensein attenuates A beta-induced cognitive deficits in rats: Enhancement of synaptic plasticity and cholinergic function

摘要

An isoflavone was isolated from Trifolium pratense using bioassay-guided screening. The structure of this natural compound was elucidated based on its spectral data, and it was identified as pratensein. The protective effect of pratensein was evaluated using a cognitive impairment model induced by injecting amyloid beta (1-42) (A beta(1-42)) into the bilateral hippocampus of rats. The results showed that pratensein treatment significantly protected against A beta(1-42)-induced cognitive impairments, as evidenced by the improvement in learning and memory and the attenuation of neuronal degeneration and apoptosis in hippocampus. Analysis of the potential mechanisms of action showed that pratensein significantly decreased inflammatory indicators such as MDA, NO, nNOS, IL-1 beta and TNF-alpha. Pratensein markedly decreased the content and deposition of beta-amyloid peptide through regulating the expressions of A beta-related genes including APP, BACE1, CatB, NEP and IDE. Moreover, pratensein significantly increased the expressions of synapse plasticity-related proteins, i.e., PSD-95, p-NMDAR1, p-CaMKII, p-PKAC beta, PKC gamma, p-CREB and BDNF. In addition, pratensein significantly decreased the activity of cholinesterase, then subsequently elevated the level of acetylcholine. In summary, our study indicated that pratensein may have a likely protective effect against Alzheimer's disease (AD) via improving synaptic plasticity and increasing cholinesterase activity. (C) 2015 Elsevier B.V. All rights reserved.