Prepulse inhibition can predict the motivational effects of cocaine in female mice exposed to maternal separation

Behav Brain Res. 2022 Jan 7:416:113545. doi: 10.1016/j.bbr.2021.113545. Epub 2021 Aug 23.

Abstract

The prepulse inhibition (PPI) of the startle response can identify the rodents that are more sensitive to the effects of cocaine. Mice with a lower PPI presented a higher vulnerability to the effects of cocaine and a higher susceptibility to developing a substance use disorder (SUD). Maternal separation with early weaning (MSEW) is a relevant animal model to induce motivational alterations throughout life. Nevertheless, only a few studies on females exist, even though they are more vulnerable to stress- and cocaine-related problems. Hence, the aim of the present study was to evaluate the ability of PPI to identify females with a greater vulnerability to the long-term consequences of early stress on the motivational effects of cocaine. Female mice underwent MSEW and were classified according to their high or low PPI. They were then assessed in the cocaine-induced locomotor sensitization test, the conditioned place preference paradigm or the operant self-administration paradigm. Additionally, they were also evaluated in the passive avoidance task, the tail-suspension and the splash tests. The results revealed that the females with lower PPI presented higher consequences of MSEW on the effects of cocaine and showed an increase in anhedonia-like behaviours. Our findings support that a PPI deficit could represent a biomarker of vulnerability to the effects of cocaine induced by MSEW.

Keywords: Anhedonia-like behaviours; Cocaine; Female mice; Maternal separation with early weaning; Prepulse inhibition; Reinforcing effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anhedonia / drug effects
  • Animals
  • Cocaine / pharmacology*
  • Conditioning, Operant / drug effects
  • Disease Models, Animal
  • Dopamine Uptake Inhibitors / pharmacology*
  • Female
  • Maternal Deprivation*
  • Mice
  • Motivation*
  • Prepulse Inhibition / drug effects*
  • Reflex, Startle / physiology*
  • Self Administration
  • Weaning

Substances

  • Dopamine Uptake Inhibitors
  • Cocaine