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Ouabain increases neuronal branching in hippocampus and improves spatial memory.
- Source :
-
Neuropharmacology [Neuropharmacology] 2018 Sep 15; Vol. 140, pp. 260-274. Date of Electronic Publication: 2018 Aug 09. - Publication Year :
- 2018
-
Abstract
- Previous research shows Ouabain (OUA) to bind Na, K-ATPase, thereby triggering a number of signaling pathways, including the transcription factors NFᴋB and CREB. These transcription factors play a key role in the regulation of BDNF and WNT-β-catenin signaling cascades, which are involved in neuroprotection and memory regulation. This study investigated the effects of OUA (10 nM) in the modulation of the principal signaling pathways involved in morphological plasticity and memory formation in the hippocampus of adult rats. The results show intrahippocampal injection of OUA 10 nM to activate the Wnt/β-Catenin signaling pathway and to increase CREB/BDNF and NFᴋB levels. These effects contribute to important changes in the cellular microenvironment, resulting in enhanced levels of dendritic branching in hippocampal neurons, in association with an improvement in spatial reference memory and the inhibition of long-term memory extinction.<br /> (Copyright © 2018. Published by Elsevier Ltd.)
- Subjects :
- Animals
Axin Protein metabolism
Brain-Derived Neurotrophic Factor metabolism
Cyclic AMP Response Element-Binding Protein metabolism
Hippocampus physiology
Male
Maze Learning
Microinjections
NF-kappa B metabolism
Neoplasm Proteins metabolism
Neuronal Plasticity drug effects
Neuronal Plasticity physiology
Nucleocytoplasmic Transport Proteins metabolism
Rats
Spatial Memory physiology
Wnt Signaling Pathway drug effects
Wnt Signaling Pathway physiology
beta Catenin metabolism
Hippocampus cytology
Hippocampus drug effects
Ouabain pharmacology
Spatial Memory drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7064
- Volume :
- 140
- Database :
- MEDLINE
- Journal :
- Neuropharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 30099050
- Full Text :
- https://doi.org/10.1016/j.neuropharm.2018.08.008