Extinction of contextual fear memory is facilitated in TRPM2 knockout mice

Transient receptor potential melastatin type 2 (TRPM2) is a nonselective cation channel involved in synaptic plasticity. We investigated its role in contextual fear conditioning and extinction of conditioned fear using Trpm2-deficient (Trpm2<sup>-/-</sup>) mice. Trpm2<sup>-/-</sup> mice exhibited reduced acquisition of contextual fear memory during conditioning but had an intact freezing response to conditioning context 24 h after conditioning. They also showed a reduced freezing response to extinction training, indicating facilitated extinction. Consistent with this, infusion of flufenamic acid (FFA), a TRPM2 antagonist, into the dentate gyrus (DG) of the hippocampus in fear-conditioned mice facilitated extinction of contextual fear. The enhanced extinction in Trpm2<sup>-/-</sup> and FFA-treated mice was associated with down-regulation of immediate-early genes (IEGs) including Npas4, c-Fos, Arc and Egr1 in the hippocampus after extinction training. Our results indicate that TRPM2 plays a positive role in retention of contextual fear memory by modulating neuronal activity in the hippocampus, and suggest that TRPM2 activity could potentially be targeted to strengthen extinction-based exposure therapies for post-traumatic stress disorder (PTSD).

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Publication Details

Journal
Molecular Brain
Published
2025-02-27
DOI
https://doi.org/10.1186/s13041-025-01181-2
Citations
2
Primary Topic
Memory and Neural Mechanisms
Type
article
Field-Weighted Citation Impact
2.86

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article

Extinction of contextual fear memory is facilitated in TRPM2 knockout mice

Huiju Lee, Hyeon Son, Seung Yeon Ko, Do Gyeong Kim et al.
2 citations
Molecular Brain
Memory and Neural Mechanisms
2.86
article

Extinction of contextual fear memory is facilitated in TRPM2 knockout mice

Huiju Lee, Hyeon Son, Seung Yeon Ko, Do Gyeong Kim, Sung Jun Jung
article en
2 citations

Abstract

Transient receptor potential melastatin type 2 (TRPM2) is a nonselective cation channel involved in synaptic plasticity. We investigated its role in contextual fear conditioning and extinction of conditioned fear using Trpm2-deficient (Trpm2<sup>-/-</sup>) mice. Trpm2<sup>-/-</sup> mice exhibited reduced acquisition of contextual fear memory during conditioning but had an intact freezing response to conditioning context 24 h after conditioning. They also showed a reduced freezing response to extinction training, indicating facilitated extinction. Consistent with this, infusion of flufenamic acid (FFA), a TRPM2 antagonist, into the dentate gyrus (DG) of the hippocampus in fear-conditioned mice facilitated extinction of contextual fear. The enhanced extinction in Trpm2<sup>-/-</sup> and FFA-treated mice was associated with down-regulation of immediate-early genes (IEGs) including Npas4, c-Fos, Arc and Egr1 in the hippocampus after extinction training. Our results indicate that TRPM2 plays a positive role in retention of contextual fear memory by modulating neuronal activity in the hippocampus, and suggest that TRPM2 activity could potentially be targeted to strengthen extinction-based exposure therapies for post-traumatic stress disorder (PTSD).

Molecular BrainVol. 18(1)
Hanyang University (KR)
National Research Foundation of Korea
Openalex Percentile: Top 12%
Memory and Neural Mechanisms
2.86
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