Stimulation of hippocampal adenylyl cyclase activity dissociates memory consolidation processes for response and place learning

  1. Guillaume Martel,
  2. Annabelle Millard1,
  3. Robert Jaffard, and
  4. Jean-Louis Guillou2
  1. Laboratoire de Neurosciences Cognitives, Université Bordeaux I, Centre Nationale de la Recherche Scientifique Unite Mixte de Recherche (CNRS UMR) 5106, 33405 Talence cedex, France

Abstract

Procedural and declarative memory systems are postulated to interact in either a synergistic or a competitive manner, and memory consolidation appears to be a highly critical stage for this process. However, the precise cellular mechanisms subserving these interactions remain unknown. To investigate this issue, 24-h retention performances were examined in mice given post-training intrahippocampal injections of forskolin (FK) aiming at stimulating hippocampal adenylyl cyclases (ACs). The injection was given at different time points over a period of 9 h following acquisition in either an appetitive bar-pressing task or water-maze tasks challenging respectively “response memory” and “place memory.” Retention testing (24 h) showed that FK injection altered memory formation only when given within a 3- to 6-h time window after acquisition but yielded opposite memory effects as a function of task demands. Retention of the spatial task was impaired, whereas retention of both the cued-response in the water maze and the rewarded bar-press response were improved. Intrahippocampal injections of FK produced an increase in pCREB immunoreactivity, which was strictly limited to the hippocampus and lasted less than 2 h, suggesting that early effects (0–2 h) of FK-induced cAMP/CREB activation can be distinguished from late effects (3–6 h). These results delineate a consolidation period during which specific cAMP levels in the hippocampus play a crucial role in enhancing memory processes mediated by other brain regions (e.g., dorsal or ventral striatum) while eliminating interference by the formation of hippocampus-dependent memory.

Footnotes

  • 1

    1 Present address: Novartis Institutes of Biomedical Research (NIBR), CH-4002 Basel, Switzerland.

  • 2

    2 Corresponding author.

    2 E-mail jl.guillou{at}lnc.u-bordeaux1.fr; fax 33-5-4000-8743.

  • Article and publication are at http://www.learnmem.org/cgi/doi/10.1101/lm.149506

    • Received November 25, 2005.
    • Accepted February 21, 2006.
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