Timp1 Deletion Induces Anxiety-like Behavior in Mice

  • Xiaotong Wang
  • , Wei Zheng
  • , Ziyi Zhu
  • , Biyu Xing
  • , Weijie Yan
  • , Ke Zhu
  • , Lingli Xiao
  • , Chaojuan Yang
  • , Mengping Wei
  • , Lei Yang
  • , Zi Bing Jin*
  • , Xueyun Bi*
  • , Chen Zhang*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The hippocampus is essential for learning and memory, but it also plays an important role in regulating emotional behavior, as hippocampal excitability and plasticity affect anxiety and fear. Brain synaptic plasticity may be regulated by tissue inhibitor of matrix metalloproteinase 1 (TIMP1), a known protein inhibitor of extracellular matrix (ECM), and the expression of TIMP1 in the hippocampus can be induced by neuronal excitation and various stimuli. However, the involvement of Timp1 in fear learning, anxiety, and hippocampal synaptic function remains to be established. Our study of Timp1 function in vivo revealed that Timp1 knockout mice exhibit anxiety-like behavior but normal fear learning. Electrophysiological results suggested that Timp1 knockout mice showed hyperactivity in the ventral CA1 region, but the basic synaptic transmission and plasticity were normal in the Schaffer collateral pathway. Taken together, our results suggest that deletion of Timp1 in vivo leads to the occurrence of anxiety behaviors, but that Timp1 is not crucial for fear learning.

Original languageEnglish
Pages (from-to)732-742
Number of pages11
JournalNeuroscience Bulletin
Volume40
Issue number6
DOIs
StatePublished - Jun 2024

Keywords

  • Anxiety
  • Fear
  • Synaptic plasticity
  • Synaptic transmission
  • Timp1

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