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The Journal of Neuroscience, August 10, 2005, 25(32):7393-7400; doi:10.1523/JNEUROSCI.0910-05.2005
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Behavioral/Systems/Cognitive
Bidirectional Modulation of Hippocampal Long-Term Potentiation under Stress and No-Stress Conditions in Basolateral Amygdala-Lesioned and Intact Rats
Volker Korz and
Julietta U. Frey
Department of Neurophysiology, Leibniz-Institute for Neurobiology, D-39118 Magdeburg, Germany
Hippocampal long-term potentiation (LTP) is widely considered as a cellular model for learning and memory formation. We have shown previously that protein synthesis-independent, early dentate gyrus (DG) LTP, lasting 4-5 h, can be transformed into a late-LTP with a duration of 24 h by a brief acute swim stress experience (high-stress condition). This reinforcement requires the activation of mineralocorticoid receptors and protein synthesis. The basolateral amygdala (BLA) is known to modulate glucocorticoid effects on the consolidation of spatial/contextual memory via a -adrenergic mechanism. Interestingly, hippocampal DG-LTP can also be indirectly modulated by -adrenergic and cholinergic/muscarinergic processes. Here, we show that the reinforcement of early-DG-LTP under high-stress conditions depends on the processing of novel spatial/contextual information. Furthermore, this reinforcement was blocked in BLA-lesioned animals compared with sham-operated and intact controls; however, it was not dependent on -adrenergic or cholinergic/muscarinergic receptor activation. In contrast, under low-stress conditions, the induction of late-LTP in BLA-lesioned animals is facilitated, and this facilitation, again, was dependent on -adrenergic activation. The data suggest that DG-LTP maintenance can be influenced by the BLA through different mechanisms: a short-lasting corticosterone-dependent and -adrenergic-independent mechanism and a long-lasting mechanism that facilitated hippocampal -adrenergic mechanisms.
Key words: basolateral amygdala; early-LTP; late-LTP; locus ceruleus; memory; stress
Received March 8, 2005;
revised June 28, 2005;
accepted June 28, 2005.
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