| Literature DB >> 25218897 |
Dong Hyun Kim1, Younghwan Lee2, Hyung Eun Lee2, Se Jin Park2, Su Jin Jeon3, Se Jin Jeon2, Jae Hoon Cheong4, Chan Young Shin5, Kun Ho Son6, Jong Hoon Ryu7.
Abstract
Memory consolidation is a process by which acquired information is transformed from a labile into a more stable state that can be retrieved at a later time. In the present study, we investigated the role of oroxylin A on the memory consolidation process in mice. Oroxylin A improved the memory retention administered at 0 h, 1 h and 3 h after training in a passive avoidance task, suggesting that oroxylin A facilitates memory consolidation. Oroxylin A increased mature brain-derived neurotrophic factor (mBDNF) levels in the hippocampus from 6h to 24h after administration. Moreover, 3h post-training administration of oroxylin A enhanced the mBDNF level at 9h after the acquisition trial compared to the level at 6h after the acquisition trial. However, 6h post-training administration of oroxylin A did not increase the mBDNF level at 9h after the acquisition trial. Blocking mBDNF signaling with recombinant tropomyosin receptor kinase B (TrkB)-Fc or k252a at 9h after the acquisition trial obstructed the effect of oroxylin A on memory consolidation. Taken together, our data suggest that oroxylin A facilitates memory consolidation through BDNF-TrkB signaling and confirms that the increase of BDNF in a specific time window plays a crucial role in memory consolidation.Entities:
Keywords: BDNF; Memory consolidation; Oroxylin A; Passive avoidance test
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Year: 2014 PMID: 25218897 DOI: 10.1016/j.brainresbull.2014.09.001
Source DB: PubMed Journal: Brain Res Bull ISSN: 0361-9230 Impact factor: 4.077