Literature DB >> 28932899

Voluntary running-enhanced synaptic plasticity, learning and memory are mediated by Notch1 signal pathway in C57BL mice.

Xiaochen Zhang1, Chunxiao Yang1, Jing Gao1, Hongqiang Yin1, Hui Zhang2, Tao Zhang2, Zhuo Yang3.   

Abstract

It is well known that voluntary running can enhance synaptic plasticity and improve learning and memory abilities. The Notch1 receptor is also reported to be associated with these processes, but its role in running-induced alterations is unclear. In this study, we aimed to investigate whether the Notch1 signalling pathway was involved in voluntary running-induced enhancement of synaptic plasticity, learning and memory. Notch1 heterozygous deficient (Notch1+/-) mice and wildtype (WT) C57BL littermates were randomly divided into runner group and non-runner group. Mice were given free access to running wheels for 14 days in both the Notch1+/- runner group and the WT runner group. Our results demonstrate that Notch1 knockdown impairs the performance in the novel object recognition (NOR) test and Morris water maze test and decreases the synaptic plasticity. Voluntary running improves spatial learning and memory abilities, promotes synaptic plasticity and increases expressions of postsynaptic proteins in WT mice but not in Notch1+/- mice. Our results suggest that Notch1 plays a vital role in spatial learning and memory, synaptic plasticity under normal physiological conditions and voluntary running conditions. These findings will set the groundwork and fill in some gaps for understanding the role of Notch1 signalling in voluntary running-induced phenomena.

Entities:  

Keywords:  Learning and memory; Notch1 receptor; Synaptic plasticity; Voluntary running

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Year:  2017        PMID: 28932899     DOI: 10.1007/s00429-017-1521-0

Source DB:  PubMed          Journal:  Brain Struct Funct        ISSN: 1863-2653            Impact factor:   3.270


  2 in total

1.  Medial prefrontal cortex Notch1 signalling mediates methamphetamine-induced psychosis via Hes1-dependent suppression of GABAB1 receptor expression.

Authors:  Tong Ni; Li Zhu; Shuai Wang; Weili Zhu; Yanxue Xue; Yingjie Zhu; Dongliang Ma; Hongyan Wang; Fanglin Guan; Teng Chen
Journal:  Mol Psychiatry       Date:  2022-06-22       Impact factor: 15.992

2.  Transcriptomics in the nucleus accumbens shell reveal sex- and reinforcer-specific signatures associated with morphine and sucrose craving.

Authors:  Hannah L Mayberry; Charlotte C Bavley; Reza Karbalaei; Drew R Peterson; Angela R Bongiovanni; Alexandra S Ellis; Sara H Downey; Andre B Toussaint; Mathieu E Wimmer
Journal:  Neuropsychopharmacology       Date:  2022-02-21       Impact factor: 8.294

  2 in total

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