Behavioral and Serotonergic Changes in the Frontal Cortex Following Methamphetamine Self-Administration

Int J Neuropsychopharmacol. 2018 Aug 1;21(8):758-763. doi: 10.1093/ijnp/pyy044.

Abstract

Background: Methamphetamine use is associated with a variety of negative health outcomes, including psychosis. The frontal cortex serotonin receptors are thought to contribute to psychosis-like behaviors. This study investigated changes in serotonergic markers in the frontal cortex following methamphetamine self-administration and hallucinogenic drug-induced behavior.

Methods: Consistent with previously published studies, freely cycling male and female rats were allowed to self-administer methamphetamine (males: 0.12 mg/infusion; females: 0.09 mg/infusion) or saline (10 µL) for 7 days. On the day following self-administration or following 10 days of extinction training, animals were given the serotonin 2A/2C agonist, 1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane hydrochloride (2 mg/kg, i.p.), and head twitches were analyzed. Autoradiography was also used to assess serotonin receptors and transporters in the frontal cortex following self-administration.

Results: Methamphetamine self-administration led to an increase in DOI-induced head-twitch behavior compared to saline only on the day following self-administration. Increases in serotonin receptors in the orbitofrontal cortex and decreases in serotonin transporters in the orbitofrontal cortex and infralimbic cortex were observed following methamphetamine self-administration as assessed by autoradiography.

Conclusions: Methamphetamine self-administration was associated with serotonergic alterations in the frontal cortex, which may underlie behavioral changes related to methamphetamine-associated psychosis.

Keywords: females; methamphetamine; self-administration; serotonin-2 receptors.

MeSH terms

  • Amphetamine-Related Disorders / complications*
  • Amphetamine-Related Disorders / metabolism
  • Amphetamine-Related Disorders / physiopathology
  • Animals
  • Behavior, Animal / drug effects*
  • Female
  • Frontal Lobe / drug effects*
  • Frontal Lobe / metabolism
  • Hallucinogens / administration & dosage
  • Hallucinogens / toxicity*
  • Male
  • Methamphetamine / administration & dosage
  • Methamphetamine / toxicity*
  • Psychoses, Substance-Induced / etiology*
  • Psychoses, Substance-Induced / metabolism
  • Psychoses, Substance-Induced / psychology
  • RNA-Binding Proteins / drug effects
  • RNA-Binding Proteins / metabolism
  • Rats, Sprague-Dawley
  • Receptors, Serotonin, 5-HT2 / drug effects
  • Receptors, Serotonin, 5-HT2 / metabolism
  • Self Administration
  • Serotonin / metabolism*
  • Time Factors

Substances

  • Hallucinogens
  • RNA-Binding Proteins
  • Receptors, Serotonin, 5-HT2
  • Sert1 protein, rat
  • Serotonin
  • Methamphetamine