Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2474487 | Acta Pharmaceutica Sinica B | 2016 | 9 Pages |
The rhizome of Gastrodia elata (GE), a herb medicine, has been used for treatment of neuronal disorders in Eastern Asia for hundreds of years. Parishin C is a major ingredient of GE. In this study, the i.c.v. injection of soluble Aβ1–42 oligomers model of LTP injury was used. We investigated the effects of parishin C on the improvement of LTP in soluble Aβ1–42 oligomer–injected rats and the underlying electrophysiological mechanisms. Parishin C (i.p. or i.c.v.) significantly ameliorated LTP impairment induced by i.c.v. injection of soluble Aβ1–42 oligomers. In cultured hippocampal neurons, soluble Aβ1–42 oligomers significantly inhibited NMDAR currents while not affecting AMPAR currents and voltage-dependent currents. Pretreatment with parishin C protected NMDA receptor currents from the damage induced by Aβ. In summary, parishin C improved LTP deficits induced by soluble Aβ1–42 oligomers. The protection by parishin C against Aβ-induced LTP damage might be related to NMDA receptors.
Graphical abstractParishin C given i.p. or i.c.v. prevented inhibitory effects of soluble Aβ1–42 oligomers on LTP induction. Soluble Aβ1–42 oligomers inhibited NMDAR currents without affecting AMPAR currents or voltage dependent currents. Parishin C pre-perfusion protected NMDAR currents from soluble Aβ1–42 oligomers.Figure optionsDownload full-size imageDownload as PowerPoint slide