» Articles » PMID: 11245703

Cellular Imaging of Zif268 Expression in the Hippocampus and Amygdala During Contextual and Cued Fear Memory Retrieval: Selective Activation of Hippocampal CA1 Neurons During the Recall of Contextual Memories

Overview
Journal J Neurosci
Specialty Neurology
Date 2001 Mar 14
PMID 11245703
Citations 145
Authors
Affiliations
Soon will be listed here.
Abstract

The neuroanatomical and molecular basis of fear memory retrieval was studied by analyzing the expression of the plasticity-associated immediate early gene zif268. Cellular quantitative in situ hybridization revealed that zif268 is expressed within specific regions of the hippocampus and amygdala during fear memory retrieval. Within the hippocampus, increased expression of zif268 was observed within CA1 neurons, but not dentate gyrus neurons, during the retrieval of contextual, but not cued, fear associations. In contrast, zif268 expression was increased within neurons of the amygdala (lateral, basal, and central nuclei) during the retrieval of both contextual and cued fear memories. These results demonstrate activation of hippocampal CA1 neurons in contextual fear memory retrieval that was not merely a correlate of the behavioral expression of fear itself, because it was limited to the retrieval of contextual, and not cued, fear memories. Further studies revealed that the selective increase in hippocampal CA1 zif268 expression seen after contextual fear memory retrieval was limited to the retrieval of recent (24 hr) but not older (28 d) memories. These experiments represent the first demonstration that zif268 expression in specific neuronal populations is associated with memory retrieval and suggest that this gene may contribute to plasticity and reconsolidation accompanying the retrieval process.

Citing Articles

Extinction of contextual fear memory is facilitated in TRPM2 knockout mice.

Ko S, Kim D, Lee H, Jung S, Son H Mol Brain. 2025; 18(1):16.

PMID: 40016847 PMC: 11869647. DOI: 10.1186/s13041-025-01181-2.


Dual-step pharmacological intervention for traumatic-like memories: implications from D-cycloserine and cannabidiol or clonidine in male and female rats.

Soares L, Nascimento L, Guimaraes F, Gazarini L, Bertoglio L Psychopharmacology (Berl). 2024; 241(9):1827-1840.

PMID: 38691149 DOI: 10.1007/s00213-024-06596-8.


Exercise induction at expression immediate early gene (c-Fos, ARC, EGR-1) in the hippocampus: a systematic review.

Rahmi U, Goenawan H, Sylviana N, Setiawan I, Putri S, Andriyani S Dement Neuropsychol. 2024; 18:e20230015.

PMID: 38628561 PMC: 11019719. DOI: 10.1590/1980-5764-DN-2023-0015.


Line- and sex-dependent effects of juvenile stress on contextual fear- and anxiety-related behavior in high- and low-alcohol-preferring mouse lines.

Mukadam A, Chester J Behav Brain Res. 2024; 463:114899.

PMID: 38342379 PMC: 10954351. DOI: 10.1016/j.bbr.2024.114899.


Neuronal types in the mouse amygdala and their transcriptional response to fear conditioning.

Hochgerner H, Singh S, Tibi M, Lin Z, Skarbianskis N, Admati I Nat Neurosci. 2023; 26(12):2237-2249.

PMID: 37884748 PMC: 10689239. DOI: 10.1038/s41593-023-01469-3.


References
1.
Mizumori S, McNaughton B, Barnes C, Fox K . Preserved spatial coding in hippocampal CA1 pyramidal cells during reversible suppression of CA3c output: evidence for pattern completion in hippocampus. J Neurosci. 1989; 9(11):3915-28. PMC: 6569931. View

2.
Killcross S, Robbins T, Everitt B . Different types of fear-conditioned behaviour mediated by separate nuclei within amygdala. Nature. 1997; 388(6640):377-80. DOI: 10.1038/41097. View

3.
Fanselow M . Contextual fear, gestalt memories, and the hippocampus. Behav Brain Res. 2000; 110(1-2):73-81. DOI: 10.1016/s0166-4328(99)00186-2. View

4.
Wilensky A, Schafe G, LeDoux J . The amygdala modulates memory consolidation of fear-motivated inhibitory avoidance learning but not classical fear conditioning. J Neurosci. 2000; 20(18):7059-66. PMC: 6772812. View

5.
Cahill L, Weinberger N, Roozendaal B, McGaugh J . Is the amygdala a locus of "conditioned fear"? Some questions and caveats. Neuron. 1999; 23(2):227-8. DOI: 10.1016/s0896-6273(00)80774-6. View