Control of recollection by slow gamma dominating mid-frequency gamma in hippocampus CA1

PLoS Biol. 2018 Jan 18;16(1):e2003354. doi: 10.1371/journal.pbio.2003354. eCollection 2018 Jan.

Abstract

Behavior is used to assess memory and cognitive deficits in animals like Fmr1-null mice that model Fragile X Syndrome, but behavior is a proxy for unknown neural events that define cognitive variables like recollection. We identified an electrophysiological signature of recollection in mouse dorsal Cornu Ammonis 1 (CA1) hippocampus. During a shocked-place avoidance task, slow gamma (SG) (30-50 Hz) dominates mid-frequency gamma (MG) (70-90 Hz) oscillations 2-3 s before successful avoidance, but not failures. Wild-type (WT) but not Fmr1-null mice rapidly adapt to relocating the shock; concurrently, SG/MG maxima (SGdom) decrease in WT but not in cognitively inflexible Fmr1-null mice. During SGdom, putative pyramidal cell ensembles represent distant locations; during place avoidance, these are avoided places. During shock relocation, WT ensembles represent distant locations near the currently correct shock zone, but Fmr1-null ensembles represent the formerly correct zone. These findings indicate that recollection occurs when CA1 SG dominates MG and that accurate recollection of inappropriate memories explains Fmr1-null cognitive inflexibility.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Brain Waves / physiology
  • CA1 Region, Hippocampal / physiology*
  • Cognition Disorders / physiopathology
  • Cognitive Dysfunction / physiopathology
  • Disease Models, Animal
  • Electrophysiological Phenomena / physiology
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Mental Retardation Protein / physiology
  • Gamma Rays
  • Gamma Rhythm / physiology
  • Hippocampus
  • Memory / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Pyramidal Cells
  • Temporal Lobe

Substances

  • Biomarkers
  • Fmr1 protein, mouse
  • Fragile X Mental Retardation Protein