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The hippocampus and prefrontal cortex are differentially involved in serial memory retrieval in non-stress and stress conditions
Authors:Frdric Chauveau  Christophe Pirard  Christophe Tronche  Mathieu Coutan  Isabelle Drouet  Pierrette Liscia  Daniel Bracocha
Institution:aCentre de Neurosciences Intégratives et Cognitives (CNIC), Universités de Bordeaux, UMR-CNRS 5228, Bâtiment Biologie Animale, Avenue des facultés, 33405 Talence Cedex, France;bInstitut de Médecine Aérospatiale du Service de Santé des Armées (IMASSA), Département de Physiologie Intégrée, BP73, 91223 Brétigny sur Orge Cedex, France
Abstract:We previously showed that 24 h after learning, mice significantly remembered the first (D1) but not the second (D2) discrimination in a serial spatial task and that an acute stress delivered 5 min before the test phase reversed this memory retrieval pattern.A first experiment evaluated the effects of dorsal hippocampus (HPC) or prefrontal cortex (PFC) lesions, these two brain areas being well-known for their involvement in serial and spatial memory processes. For this purpose, six independent groups of mice were used: non-lesioned (controls), PFC or HPC-lesioned animals, submitted or not to an acute stress (electric footshocks; 0.9 mA). Results show that (i) non-stressed controls as well as PFC-lesioned mice (stressed or not) remembered D1 but not D2; (ii) stressed controls and HPC-lesioned mice (stressed or not) remembered D2 but not D1; (iii) stress significantly increased plasma corticosterone in controls and PFC-lesioned mice, but not in HPC-lesioned mice which already showed a significant plasma corticosterone increase in non-stressed condition.Since data from this first experiment showed that stress inhibited the hippocampal-dependent D1 memory retrieval, a second experiment evaluated the behavioral effect of intrahippocampal corticosterone injection in non-stressed mice. Results show that intrahippocampal corticosterone injection induced a reversal of serial memory retrieval pattern similar to that induced by acute stress.Overall, our study shows that (i) in non-stress condition, the emergence of D1 is HPC-dependent; (ii) in stress condition, the emergence of D2 requires the PFC integrity; moreover, intrahippocampal corticosterone injection mimicked the effects of stress in the CSD task.
Keywords:Acute stress  Serial spatial memory  Memory retrieval  Hippocampus  Prefrontal cortex  Glucocorticoids  Corticosterone  Mice
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