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European Journal of Neuroscience 13 (7), 1453-1458

 

Fear memory retrieval induces CREB phosphorylation and Fos expression within the amygdala
Jeremy Hall, Kerrie L. Thomas and Barry J. Everitt

 

Abstract

Fear memory retrieval has been shown to induce a protein-synthesis dependent re-consolidation of memories within the amygdala. Here, using immunocytochemistry, we investigated the molecular basis of this process in the rat and show that retrieval of a cued fear memory induces the activation, by phosphorylation, of the transcription factor CREB within the basal and lateral nuclei of the amygdala, as well as expression of the CREB-regulated immediate-early gene, c-fos, in the basal amygdala. We also show an increase in CREB phosphorylation within the central nucleus of the amygdala following behavioural testing, with an accompanying increase in Fos-immunoreactive nuclei in animals retrieving the cued association. There were no changes in either phosphorylated CREB or Fos in the hippocampus following exposure to discrete fear stimuli. These results show that activation of CREB, which has been shown to be involved in the formation of long-term fear memories, also accompanies memory retrieval, and also suggest a role for CREB phosphorylation in memory re-consolidation following retrieval.

Keywords: gene expression, hippocampus, learning and memory, rat

Correspondence: Dr Kerrie Thomas, as above. E-mail: klt25@cus.cam.ac.uk

AbbreviationsAB, accessory basal nucleus of the amygdala; B, basal nucleus of the amygdala; CeN, central nucleus of the amygdala; CRE, calcium and cAMP response element; CREB, calcium and cAMP response element binding protein; CS, conditioned stimulus; DG, dentate gyrus; IEG, immediate-early gene; IR, immunoreactive; LA, lateral nucleus of the amygdala; pCREB, phosphorylated calcium and cAMP response element binding protein; PB, phosphate buffer; PFA, paraformaldehyde; US, unconditioned stimulus.

Received 8 December 2000, revised 1 February 2001, accepted 5 February 2001

 

 


 
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