Anxiety, aggression, reward sensitivity, and forebrain dopamine receptor expression in a laboratory rat model of early-life disadvantage

Dev Psychobiol. 2023 Nov;65(7):e22421. doi: 10.1002/dev.22421.

Abstract

Despite early-life disadvantage (ELD) in humans being a highly heterogenous construct, it consistently predicts negative neurobehavioral outcomes. The numerous environmental contributors and neural mechanisms underlying ELD remain unclear, though. We used a laboratory rat model to evaluate the effects of limited resources and/or heavy metal exposure on mothers and their adult male and female offspring. Dams and litters were chronically exposed to restricted (1-cm deep) or ample (4-cm deep) home cage bedding postpartum, with or without lead acetate (0.1%) in their drinking water from insemination through 1-week postweaning. Restricted-bedding mothers showed more pup-directed behaviors and behavioral fragmentation, while lead-exposed mothers showed more nestbuilding. Restricted bedding-raised male offspring showed higher anxiety and aggression. Either restricted bedding or lead exposure impaired goal-directed performance in a reinforcer devaluation task in females, whereas restricted bedding alone disrupted it in males. Lead exposure, but not limited bedding, also reduced sucrose reward sensitivity in a progressive ratio task in females. D1 and D2 receptor mRNA in the medial prefrontal cortex and nucleus accumbens (NAc) were each affected by the early-life treatments and differently between the sexes. Most notably, adult males (but not females) exposed to both early-life treatments had greatly increased D1 receptor mRNA in the NAc core. These results illuminate neural mechanisms through which ELD threatens neurobehavioral development and highlight forebrain dopamine as a factor.

Keywords: anxiety; development; dopamine; heavy metals; maternal behavior; stress; teratogens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggression
  • Animals
  • Anxiety
  • Dopamine* / metabolism
  • Female
  • Humans
  • Lead / metabolism
  • Lead / pharmacology
  • Male
  • Nucleus Accumbens / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Receptors, Dopamine* / metabolism
  • Reward

Substances

  • Dopamine
  • Receptors, Dopamine
  • Lead
  • RNA, Messenger