Metformin in nucleus accumbens core reduces cue-induced cocaine seeking in male and female rats

Addict Biol. 2022 May;27(3):e13165. doi: 10.1111/adb.13165.

Abstract

This study investigated the potential therapeutic effects of the FDA-approved drug metformin on cue-induced reinstatement of cocaine seeking. Metformin (dimethyl-biguanide) is a first-line treatment for type II diabetes that, among other mechanisms, is involved in the activation of adenosine monophosphate activated protein kinase (AMPK). Cocaine self-administration and extinction is associated with decreased levels of phosphorylated AMPK within the nucleus accumbens core (NAcore). Previously, it was shown that increasing AMPK activity in the NAcore decreased cue-induced reinstatement of cocaine seeking. Decreasing AMPK activity produced the opposite effect. The goal of the present study was to determine if metformin in the NAcore reduces cue-induced cocaine seeking in adult male and female Sprague Dawley rats. Rats were trained to self-administer cocaine followed by extinction prior to cue-induced reinstatement trials. Metformin microinjected in the NAcore attenuated cue-induced reinstatement in male and female rats. Importantly, metformin's effects on cocaine seeking were not due to a general depression of spontaneous locomotor activity. In female rats, metformin's effects did generalize to a reduction in cue-induced reinstatement of sucrose seeking. These data support a potential role for metformin as a pharmacotherapy for cocaine use disorder but warrant caution given the potential for metformin's effects to generalize to a natural reward in female rats.

Keywords: cocaine; metformin; nucleus accumbens; reinstatement; self-administration.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Cocaine*
  • Cues
  • Diabetes Mellitus, Type 2* / metabolism
  • Female
  • Male
  • Metformin* / metabolism
  • Metformin* / pharmacology
  • Nucleus Accumbens
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Metformin
  • AMP-Activated Protein Kinases
  • Cocaine