Extinction of contextual fear memory is facilitated in TRPM2 knockout miceopen access
- Authors
- Ko, Seung Yeon; Kim, Do Gyeong; Lee, Huiju; Jung, Sung Jun; Son, Hyeon
- Issue Date
- Dec-2025
- Publisher
- BioMed Central
- Keywords
- Transient receptor potential melastatin type 2 (TRPM2); Extinction; Fear memory
- Citation
- Molecular Brain, v.18, no.1, pp 1 - 12
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Molecular Brain
- Volume
- 18
- Number
- 1
- Start Page
- 1
- End Page
- 12
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/212594
- DOI
- 10.1186/s13041-025-01181-2
- ISSN
- 1756-6606
1756-6606
- 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-/-) mice. Trpm2-/- 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-/- 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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