Dopamine transporter mRNA in autopsy studies of chronic cocaine users

Brain Res Mol Brain Res. 1999 Nov 10;73(1-2):181-5. doi: 10.1016/s0169-328x(99)00233-8.

Abstract

The effects of chronic cocaine abuse on transcriptional regulation of human dopamine transporter (DAT) mRNA in midbrain dopaminergic neurons was assessed by reverse transcription-polymerase chain reaction (RT-PCR). DAT/cyclophilin mRNA ratios in the substantia nigra (SN) were unchanged in cocaine overdose (CO) victims as compared to age-matched and drug-free control (CTRL) subjects. In contrast, DAT mRNA levels were decreased significantly in agitated cocaine delirium victims (67%, p<0.05). These findings demonstrate the lack of a regulatory influence by cocaine on the steady state content of DAT mRNA in cocaine abusers. In contrast, DAT gene expression was altered significantly in cocaine abusers at risk for agitated delirium.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Autopsy
  • Carrier Proteins / genetics*
  • Case-Control Studies
  • Chronic Disease
  • Cocaine / adverse effects
  • Cocaine-Related Disorders / genetics*
  • Cocaine-Related Disorders / pathology
  • Delirium / chemically induced
  • Delirium / genetics
  • Delirium / pathology
  • Dopamine Plasma Membrane Transport Proteins
  • Drug Overdose
  • Female
  • Gene Expression Regulation / drug effects
  • Humans
  • Male
  • Membrane Glycoproteins*
  • Membrane Transport Proteins*
  • Nerve Tissue Proteins*
  • Peptidylprolyl Isomerase / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Substantia Nigra / metabolism

Substances

  • Carrier Proteins
  • Dopamine Plasma Membrane Transport Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • RNA, Messenger
  • SLC6A3 protein, human
  • Peptidylprolyl Isomerase
  • Cocaine