Serotonin-transporter mediated efflux: a pharmacological analysis of amphetamines and non-amphetamines

Neuropharmacology. 2005 Nov;49(6):811-9. doi: 10.1016/j.neuropharm.2005.08.008. Epub 2005 Sep 26.

Abstract

The physiological function of neurotransmitter transporter proteins like the serotonin transporter (SERT) is reuptake of neurotransmitter that terminates synaptic serotoninergic transmission. SERT can operate in reverse direction and be induced by SERT substrates including 5-HT, tyramine and the positively charged methyl-phenylpyridinium (MPP(+)), as well as the amphetamine derivatives para-chloroamphetamine (pCA) and methylene-dioxy-methamphetamine (MDMA). These substrates also induce inwardly directed sodium currents that are predominantly carried by sodium ions. Efflux via SERT depends on this sodium flux that is believed to be a prerequisite for outward transport. However, in recent studies, it has been suggested that substrates may be distinct in their properties to induce efflux. Therefore, the aim of the present study was a pharmacological characterization of different SERT substrates in uptake experiments, their abilities to induce transporter-mediated efflux and currents. In conclusion, the rank order of affinities in uptake and electrophysiological experiments correlate well, while the potencies of the amphetamine derivatives for the induction of efflux are clearly higher than those of the other substrates. These discrepancies can be only explained by mechanisms that can be induced by amphetamines. Therefore, based on our pharmacological observations, we conclude that amphetamines distinctly differ from non-amphetamine SERT substrates.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamine / pharmacology*
  • Biological Transport / drug effects
  • Cell Line
  • Dopamine Uptake Inhibitors / pharmacology*
  • Dose-Response Relationship, Drug
  • Electric Stimulation / methods
  • Humans
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Membrane Potentials / radiation effects
  • N-Methyl-3,4-methylenedioxyamphetamine / pharmacology
  • Patch-Clamp Techniques / methods
  • Serotonin / metabolism*
  • Serotonin Agents / pharmacology
  • Serotonin Plasma Membrane Transport Proteins / physiology*
  • Serotonin Uptake Inhibitors / pharmacokinetics
  • Serotonin Uptake Inhibitors / pharmacology
  • Time Factors
  • Transfection
  • Tritium / pharmacokinetics
  • Tyramine / pharmacokinetics

Substances

  • Dopamine Uptake Inhibitors
  • Serotonin Agents
  • Serotonin Plasma Membrane Transport Proteins
  • Serotonin Uptake Inhibitors
  • Tritium
  • Serotonin
  • Amphetamine
  • N-Methyl-3,4-methylenedioxyamphetamine
  • Tyramine