Ecstasy--long-term effects on the human central nervous system revealed by positron emission tomography

Br J Psychiatry. 1999 Aug:175:186-8. doi: 10.1192/bjp.175.2.186.

Abstract

Background: The main psychotropic agent of the popular illicit drug ecstasy is 3,4-methylenedioxymethamphetamine (MDMA). In the light of animal studies and examinations of human cerebrospinal fluid, MDMA is suspected of causing neurotoxic lesions to the serotonergic system.

Aims: To postulate a relationship between ecstasy use and lasting alterations to the cerebral glucose metabolic rate.

Method: Positron emission tomography (PET) with 2-[18F]-fluoro-2-deoxy-D-glucose (FDG) was performed on seven ecstasy users and seven subjects without any known history of illicit drug use. Data were compared for a limited number of brain regions.

Results: By comparison with the control group, the glucose metabolic uptake of the ecstasy user group was altered within the amygdala, hippocampus and Brodmann's area II.

Conclusions: The results suggest the possibility that ecstasy use has lasting effects on central neuronal activity in humans.

MeSH terms

  • Adult
  • Case-Control Studies
  • Central Nervous System Diseases / chemically induced*
  • Central Nervous System Diseases / diagnostic imaging
  • Central Nervous System Diseases / metabolism
  • Female
  • Fluorodeoxyglucose F18
  • Glucose / metabolism
  • Hallucinogens / adverse effects*
  • Humans
  • Male
  • N-Methyl-3,4-methylenedioxyamphetamine / adverse effects*
  • Tomography, Emission-Computed / methods

Substances

  • Hallucinogens
  • Fluorodeoxyglucose F18
  • Glucose
  • N-Methyl-3,4-methylenedioxyamphetamine