Journal of Neuroscience · 2014 · 15 citations · 26 references
Life SciencesNeurobiologyNeuroscienceMolecular NeuroscienceNeuroplasticitySynaptic PlasticityHippocampal CircuitsHippocampal SystemsLong-term PotentiationStructural Synaptic PlasticitySynaptic Strength RegulationSynaptic TransmissionExplorationHippocampal Circuit OrganizationHippocampal CircuitryHippocampal LearningHippocampal Long-term PotentiationLong-term Synaptic PlasticityPlasticity At Excitatory SynapsesRodent Synaptic Plasticity
Recent work showed that unsupervised learning of a complex environment activates synaptic proteins essential for the stabilization of long-term potentiation (LTP). The present study used automated methods to construct maps of excitatory synapses associated with high concentrations of one of these LTP-related proteins [CaMKII phosphorylated at T286/287, (pCaMKII)]. Labeling patterns across 42 sampling zones covering entire cross sections through rostral hippocampus were assessed for two groups of rats that explored a novel two-room arena for 30 min, with or without a response contingency involving mildly aversive cues. The number of pCaMKII-immunopositive (+) synapses was highly correlated between the two groups for the 21 sampling zones covering the dentate gyrus, CA3c/hilus, and apical dendrites of field CA1, but not for the remainder of the cross section. The distribution of pCaMKII+ synapses in the large uncorrelated segment differed markedly between the groups. Subtracting home-cage values removed high scores (i.e., sampling zones with a high percentage of pCaMKII+ contacts) in the negative contingency group, but not in the free-exploration animals. Three sites in the latter had values that were markedly elevated above other fields. These mapping results suggest that encoding of a form of memory that is dependent upon rostral hippocampus reliably occurs at high levels in discrete anatomical zones, and that this regionally differentiated response is blocked when animals are inhibited from freely exploring the environment by the introduction of a mildly aversive stimulus.
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The hippocampal CA3 network: An in vivo intracellular labeling study
X.‐G. Li, Péter Somogyi, Aarne Ylinen et al. · The Journal of Comparative Neurology · 1994 · 769 citations