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Research ArticleCELLULAR AND MOLECULAR

Molecular Mechanism of Citalopram and Cocaine Interactions with Neurotransmitter Transporters

Aina Westrheim Ravna, Ingebrigt Sylte and Svein G. Dahl
Journal of Pharmacology and Experimental Therapeutics October 2003, 307 (1) 34-41; DOI: https://doi.org/10.1124/jpet.103.054593
Aina Westrheim Ravna
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Ingebrigt Sylte
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Svein G. Dahl
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Abstract

The selective serotonin reuptake inhibitors (SSRIs) and cocaine bind to the neural serotonin (5-HT) transporter (SERT) and thus inhibit presynaptic reuptake of 5-HT and elevate its concentration in the synaptic cleft. Cocaine also binds to the dopamine transporter (DAT) and to the noradrenaline transporter (NET) and inhibits presynaptic reuptake of dopamine and noradrenaline. SERT, DAT, and NET belong to the sodium/neurotransmitter symporter family, which is predicted to have a molecular structure with 12 transmembrane α-helices (TMHs) and intracellular amino- and carboxy terminals. We used an electron density projection map of the Escherichia coli Na+/H+ anti-porter, and site-directed mutagenesis data on DAT and SERT to construct 3-dimensional molecular models of SERT, DAT and NET. These models were used to simulate the molecular interaction mechanisms of the SSRI, S-citalopram, its less potent enantiomer, R-citalopram and of cocaine with the transporters. In the SERT model, a single amino acid (Tyr95) in TMH1 determined the transporter selectivity of S-citalopram for SERT over DAT and NET. A dipole-dipole interaction was formed between the hydroxy group of Tyr95 in SERT and the nitril group of S-citalopram, but could not be formed by S-citalopram in DAT and NET where the corresponding amino acid is a phenylalanine. The lower binding affinity of R-citalopram may be due to sterical hindrance at the binding site. The tropane ring of cocaine interacted with Tyr95 in SERT and with the corresponding phenylalanines in NET and DAT. This may explain why cocaine, but not S-citalopram, has high binding affinity to all three transporters.

Footnotes

  • The present study was supported by computer time on the HP RISC super-computer at the University of Tromsø (Tromsø, Norway).

  • DOI: 10.1124/jpet.103.054593.

  • ABBREVIATIONS: 5-HT, serotonin; SSRIs, serotonin reuptake inhibitors; SERT, serotonin transporter; NET, noradrenaline transporter; DAT, dopamine transporter; SNF, sodium/neurotransmitter symporter family; TMH, transmembrane α-helix; NhaA, Na+/H+ antiporter; lac permease, lactose permease symporter; MD, molecular dynamics; PDB, protein data bank; GPCR, G-protein coupled receptors; RTI-233, N-(N-methyl-N-(4-nitrobenzo-2-oxa-1,3-diazol-7-yl)ethanolamine ester hydrochloride.

    • Received May 20, 2003.
    • Accepted June 20, 2003.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 307 (1)
Journal of Pharmacology and Experimental Therapeutics
Vol. 307, Issue 1
1 Oct 2003
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Research ArticleCELLULAR AND MOLECULAR

Molecular Mechanism of Citalopram and Cocaine Interactions with Neurotransmitter Transporters

Aina Westrheim Ravna, Ingebrigt Sylte and Svein G. Dahl
Journal of Pharmacology and Experimental Therapeutics October 1, 2003, 307 (1) 34-41; DOI: https://doi.org/10.1124/jpet.103.054593

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Research ArticleCELLULAR AND MOLECULAR

Molecular Mechanism of Citalopram and Cocaine Interactions with Neurotransmitter Transporters

Aina Westrheim Ravna, Ingebrigt Sylte and Svein G. Dahl
Journal of Pharmacology and Experimental Therapeutics October 1, 2003, 307 (1) 34-41; DOI: https://doi.org/10.1124/jpet.103.054593
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