Behaviour-driven Arc expression is greater in dorsal than ventral CA1 regardless of task or sex differences

Behav Brain Res. 2022 Apr 9:423:113790. doi: 10.1016/j.bbr.2022.113790. Epub 2022 Feb 8.

Abstract

Evidence from genetic, behavioural, anatomical, and physiological study suggests that the hippocampus functionally differs across its longitudinal (dorsoventral or septotemporal) axis. Although, how to best characterize functional and representational differences in the hippocampus across its long axis remains unclear. While some suggest that the hippocampus can be divided into dorsal and ventral subregions that support distinct cognitive functions, others posit that these regions vary in their granularity of representation, wherein spatial-temporal resolution decreases in the ventral (temporal) direction. Importantly, the cognitive and granular hypotheses also make distinct predictions on cellular recruitment dynamics under conditions when animals perform tasks with qualitatively different cognitive-behavioural demands. One interpretation of the cognitive function account implies that dorsal and ventral cellular recruitment differs depending on relevant behavioural demands, while the granularity account suggests similar recruitment dynamics regardless of the nature of the task performed. Here, we quantified cellular recruitment with the immediate early gene (IEG) Arc across the entire longitudinal CA1 axis in female and male rats performing spatial- and fear-guided memory tasks. Our results show that recruitment is greater in dorsal than ventral CA1 regardless of task or sex, and thus support a granular view of hippocampal function across the long axis. We further discuss how future experiments might determine the relative contributions of cognitive function and granularity of representation to neuronal activity dynamics in hippocampal circuits.

Keywords: Arc; CA1; Hippocampus; Immediate early genes; Longitudinal axis; Memory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / physiology*
  • CA1 Region, Hippocampal / metabolism*
  • Cytoskeletal Proteins / metabolism*
  • Female
  • Learning / physiology*
  • Male
  • Nerve Tissue Proteins / metabolism*
  • Rats
  • Rats, Long-Evans
  • Sex Characteristics
  • Task Performance and Analysis

Substances

  • Cytoskeletal Proteins
  • Nerve Tissue Proteins
  • activity regulated cytoskeletal-associated protein