2022/03/25 by Sean Knight, Knight, Sean
Neuroscience · #FOS: Biological sciences #Memory and Neural Mechanisms #Neurons and Cognition (q-bio.NC) #Neuroscience and Neuropharmacology Research
paper · pdf · doi:10.48550/arxiv.2203.13434
openalex publication_date 2022/03/25 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/28
Spatial learning across many species is impaired by lesions in the hippocampus, a subcortical brain structure whose cellular composition changes substantially over its 5 to 6 week lifetime from mainly excitatory neurons during development to equal proportions of inhibitory interneurons (gamma Amp/Arcs) as well as pyramidal cells early in life, but which later on comprises only about 10% Arches+ projection spiny cortical projecting principal cells that are located within discrete cytoarchitectonic patches known as CA3 or just hilus granular layer 2 (CG2). While other structures may contribute importantly in certain situations e.g., perirhinal cortex when using visual cues with no reference frame for location), these remaining cell types also change their proportion through time with gamma APs forming 30 to 35 percent), fast firing parvalbumin immunoreactive basket or axoaxonic synapses into somatic spines at 40 days after birth (DABs formed into spine membranes by 15 DAB), and CG2 pyramids forming relatively slowly but strengthening synapses onto nearby dendritic shafts made up largely (>80 %) by GABAergic terminals (+spines) until then that were still synaptically silent.