Corticosterone in the dorsolateral striatum facilitates the extinction of stimulus-response memory

Neurobiol Learn Mem. 2021 Sep:183:107481. doi: 10.1016/j.nlm.2021.107481. Epub 2021 Jun 21.

Abstract

Glucocorticoid hormones are crucially involved in modulating mnemonic processing of stressful or emotionally arousing experiences. They are known to enhance the consolidation of new memories, including those that extinguish older memories. In this study, we investigated whether glucocorticoids facilitate the extinction of a striatum-dependent, and behaviorally more rigid, stimulus-response memory. For this, male rats were initially trained for six days on a stimulus-response task in a T-maze to obtain a reward after making an egocentric right-turn body response, regardless of the starting position in this maze. This training phase was followed by three extinction sessions in which right-turn body responses were not reinforced. Corticosterone administration into the dorsolateral region of the striatum after the first extinction session dose-dependently enhanced the consolidation of extinction memory: Rats administered the higher dose of corticosterone (30 ng), but not lower doses (5 or 10 ng), exhibited significantly fewer right-turn body responses and had longer latencies compared to vehicle-treated animals on the second and third extinction sessions. Co-administration of the glucocorticoid receptor antagonist RU 486 (10 ng) prevented the corticosterone effect, indicating that glucocorticoids enhance the extinction of stimulus-response memory via activation of the glucocorticoid receptor. Corticosterone administration into the dorsomedial striatum did not affect extinction memory. These findings indicate that stress-response mechanisms involving corticosterone actions in the dorsolateral striatum facilitate the extinction of stimulus-response memory that might allow for the development of an opportune behavioral strategy.

Keywords: Corticosterone; Dorsolateral striatum; Extinction; Glucocorticoid receptor; Response behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism
  • Corpus Striatum / pathology
  • Corticosterone / pharmacology*
  • Extinction, Psychological / drug effects*
  • Glucocorticoids / pharmacology*
  • Hormone Antagonists / pharmacology
  • Male
  • Maze Learning
  • Memory / drug effects*
  • Memory Consolidation / drug effects
  • Mifepristone / pharmacology
  • Neostriatum / drug effects*
  • Neostriatum / metabolism
  • Neostriatum / pathology
  • Rats
  • Receptors, Glucocorticoid / antagonists & inhibitors
  • Receptors, Glucocorticoid / metabolism*

Substances

  • Glucocorticoids
  • Hormone Antagonists
  • Receptors, Glucocorticoid
  • Mifepristone
  • Corticosterone