Alcohol-specific transcriptional dynamics of memory reconsolidation and relapse.
Alcohol-specific transcriptional dynamics of memory reconsolidation and relapse.
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DOI:
10.1038/s41398-023-02352-2
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发表时间:
2023-02-15
影响因子:
6.8
通讯作者:
Barak, Segev
中科院分区:
文献类型:
--
作者:
Goltseker, Koral;Garay, Patricia;Bonefas, Katherine;Iwase, Shigeki;Barak, Segev
Relapse, a critical issue in alcohol addiction, can be attenuated by disruption of alcohol-associated memories. Memories are thought to temporarily destabilize upon retrieval during the reconsolidation process. Here, we provide evidence for unique transcriptional dynamics underpinning alcohol memory reconsolidation. Using a mouse place-conditioning procedure, we show that alcohol-memory retrieval increases the mRNA expression of immediate-early genes in the dorsal hippocampus and medial prefrontal cortex, and that alcohol seeking is abolished by post-retrieval non-specific inhibition of gene transcription, or by downregulating ARC expression using antisense-oligodeoxynucleotides. However, since retrieval of memories for a natural reward (sucrose) also increased the same immediate-early gene expression, we explored for alcohol-specific transcriptional changes using RNA-sequencing. We revealed a unique transcriptional fingerprint activated by alcohol memories, as the expression of this set of plasticity-related genes was not altered by sucrose-memory retrieval. Our results suggest that alcohol memories may activate two parallel transcription programs: one is involved in memory reconsolidation in general, and another is specifically activated during alcohol-memory processing.
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影响因子:
3.4
作者:
Exton-McGuinness MT;Lee JL
通讯作者:
Lee JL
影响因子:
3.1
作者:
Antoine, Besnard;Serge, Laroche;Jocelyne, Caboche
通讯作者:
Jocelyne, Caboche
影响因子:
25
作者:
Baunez, C;Dias, C;Amalric, M
通讯作者:
Amalric, M
影响因子:
4.7
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George O;Hope BT
通讯作者:
Hope BT
影响因子:
64.8
作者:
Collins, Pamela Y.;Patel, Vikram;Joestl, Sarah S.;March, Dana;Insel, Thomas R.;Daar, Abdallah S.
通讯作者:
Daar, Abdallah S.