Reactivation of fear memory renders consolidated amygdala synapses labile

Jeongyeon Kim, Beomjong Song, Ingie Hong, Jihye Kim, Junuk Lee, Sungmo Park, Jae Yong Eom, Changjoon Lee, Sukwon Lee, Sukwoo Choi

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

It is believed that memory reactivation transiently renders consolidated memory labile and that this labile or deconsolidated memory is reconsolidated in a protein synthesis-dependent manner. The synaptic correlate of memory deconsolidation upon reactivation, however, has not been fully characterized. Here, we show that 3,5-dihydroxyphenylglycine (DHPG), an agonist for group I metabotropic glutamate receptors (mGluRI), induces synaptic depotentiation only at thalamic input synapses onto the lateral amygdala (T-LA synapses) where synaptic potentiation is consolidated, but not at synapses where synaptic potentiation is not consolidated. Using this mGluRI-induced synaptic depotentiation (mGluRI-depotentiation) as a marker of consolidated synapses, we found that mGluRI-depotentiation correlated well with the state of memory deconsolidation and reconsolidation in a predictable manner. DHPG failed to induce mGluRI-depotentiation in slices prepared immediately after reactivation when the reactivated memory was deconsolidated. DHPG induced mGluRI-depotentiation 1 h after reactivation when the reactivated memory was reconsolidated, but it failed to do so when reconsolidation was blocked by a protein synthesis inhibitor. To test the memory-specificity of mGluRI-depotentiation, conditioned fear was acquired twice using two discriminative tones (2.8 and 20 kHz). Under this condition, mGluRI-depotentiation was fully impaired in slices prepared immediately after reactivation with both tones, whereas mGluRI-depotentiation was partially impaired immediately after reactivation with the 20 kHz tone. Consistently, microinjection of DHPG into the LA1 h after reactivation reduced fear memory retention, whereas DHPG injection immediately after reactivation failed to do so. Our findings suggest that, upon memory reactivation, consolidated T-LA synapses enter a temporary labile state, displaying insensitivity to mGluRI-depotentiation.

Original languageEnglish
Pages (from-to)9631-9640
Number of pages10
JournalJournal of Neuroscience
Volume30
Issue number28
DOIs
Publication statusPublished - 2010 Jul 14
Externally publishedYes

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Long-Term Synaptic Depression
Amygdala
Synapses
Fear
Metabotropic Glutamate Receptors
Protein Synthesis Inhibitors
Microinjections

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Kim, J., Song, B., Hong, I., Kim, J., Lee, J., Park, S., ... Choi, S. (2010). Reactivation of fear memory renders consolidated amygdala synapses labile. Journal of Neuroscience, 30(28), 9631-9640. https://doi.org/10.1523/JNEUROSCI.0940-10.2010

Reactivation of fear memory renders consolidated amygdala synapses labile. / Kim, Jeongyeon; Song, Beomjong; Hong, Ingie; Kim, Jihye; Lee, Junuk; Park, Sungmo; Eom, Jae Yong; Lee, Changjoon; Lee, Sukwon; Choi, Sukwoo.

In: Journal of Neuroscience, Vol. 30, No. 28, 14.07.2010, p. 9631-9640.

Research output: Contribution to journalArticle

Kim, J, Song, B, Hong, I, Kim, J, Lee, J, Park, S, Eom, JY, Lee, C, Lee, S & Choi, S 2010, 'Reactivation of fear memory renders consolidated amygdala synapses labile', Journal of Neuroscience, vol. 30, no. 28, pp. 9631-9640. https://doi.org/10.1523/JNEUROSCI.0940-10.2010
Kim, Jeongyeon ; Song, Beomjong ; Hong, Ingie ; Kim, Jihye ; Lee, Junuk ; Park, Sungmo ; Eom, Jae Yong ; Lee, Changjoon ; Lee, Sukwon ; Choi, Sukwoo. / Reactivation of fear memory renders consolidated amygdala synapses labile. In: Journal of Neuroscience. 2010 ; Vol. 30, No. 28. pp. 9631-9640.
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