Beta-lactam antibiotic decreases acquisition of and motivation to respond for cocaine, but not sweet food, in C57Bl/6 mice

Behav Pharmacol. 2011 Aug;22(4):370-3. doi: 10.1097/FBP.0b013e3283473c10.

Abstract

No medication is approved to treat cocaine addiction, but mounting evidence suggests that glutamate-directed approaches may reduce cocaine dependence and relapse. We tested the hypotheses that the glutamate transporter subtype 1 activator, ceftriaxone, disrupts acquisition of cocaine self-administration, motivation to self-administer cocaine, and conditioned place preference in mice. Repeated ceftriaxone (200 mg/kg) reduced the ability of mice to acquire cocaine and the motivation to self-administer cocaine after successful acquisition without affecting acquisition of or motivation for sweet food. Repeated ceftriaxone had no effect on cocaine-conditioned place preference. These results suggest that a β-lactam antibiotic reduces the direct reinforcing strength of cocaine without producing nonspecific deficits in conditioned learning processes.

Publication types

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

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Ceftriaxone / pharmacology
  • Cocaine / pharmacology*
  • Cocaine-Related Disorders / psychology*
  • Conditioning, Operant / drug effects*
  • Dose-Response Relationship, Drug
  • Excitatory Amino Acid Transporter 2 / metabolism
  • Food*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Motivation / drug effects*
  • Reinforcement Schedule
  • Reinforcement, Psychology
  • Reward
  • Self Administration
  • beta-Lactams / pharmacology*

Substances

  • Anti-Bacterial Agents
  • Excitatory Amino Acid Transporter 2
  • Slc1a2 protein, mouse
  • beta-Lactams
  • Ceftriaxone
  • Cocaine