Dopaminergic modulation of reward discounting in healthy rats: a systematic review and meta-analysis

Psychopharmacology (Berl). 2021 Mar;238(3):711-723. doi: 10.1007/s00213-020-05723-5. Epub 2020 Nov 19.

Abstract

Rationale: Although numerous studies have suggested that pharmacological alteration of the dopamine (DA) system modulates reward discounting, these studies have produced inconsistent findings.

Objectives: Here, we conducted a systematic review and pre-registered meta-analysis to evaluate DA drug-mediated effects on reward discounting of time, probability, and effort costs in studies of healthy rats. This produced a total of 1343 articles to screen for inclusion/exclusion. From the literature, we identified 117 effects from approximately 1549 individual rats.

Methods: Using random effects with maximum-likelihood estimation, we meta-analyzed placebo-controlled drug effects for (1) DA D1-like receptor agonists and (2) antagonists, (3) D2-like agonists and (4) antagonists, and (5) DA transporter-modulating drugs.

Results: Meta-analytic effects showed that DAT-modulating drugs decreased reward discounting. While D1-like and D2-like antagonists both increased discounting, agonist drugs for those receptors had no significant effect on discounting behavior. A number of these effects appear contingent on study design features like cost type, rat strain, and microinfusion location.

Conclusions: These findings suggest a nuanced relationship between DA and discounting behavior and urge caution when drawing generalizations about the effects of pharmacologically manipulating dopamine on reward-based decision-making.

Keywords: Decision-making; Delay; Discounting; Dopamine; Effort; Meta-analysis; Pharmacology; Probability.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Animals
  • Biological Transport
  • Brain / drug effects
  • Brain / metabolism
  • Decision Making / drug effects*
  • Delay Discounting / drug effects*
  • Dopamine Agonists / pharmacology*
  • Dopamine Antagonists / pharmacology*
  • Dose-Response Relationship, Drug
  • Male
  • Rats
  • Receptors, Dopamine D1 / metabolism*
  • Receptors, Dopamine D2 / metabolism*
  • Reward*

Substances

  • Dopamine Agonists
  • Dopamine Antagonists
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2