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Cheerful news for antidepressant research


09 August 2007

Two research groups have independently reported new findings on the mechanism of action of an important class of antidepressant drugs. The work provides key insights into how tricyclic antidepressants interfere with neurophysiology at the molecular scale, and could eventually open the way to the development of more efficient therapies.

Tricyclic antidepressants (TCAs) are molecules that resemble a kite, with a central seven-membered ring trailing a short tail and flanked by two benzene rings. TCAs work by inhibiting neurons from taking up the monoamine neurotransmitters serotonin, norepinephrine and dopamine, which regulate mood. By blocking the re-uptake of these transmitters by their specific transporter proteins, the transmitter molecules remain in circulation for longer, prolonging their action.

However, the precise way in which the drugs work had remained unresolved. Now, Maarten Reith, Da-Neng Wang and colleagues1 at the New York University School of Medicine, US, and a team led by Eric Gouaux2 at the Oregon Health and Science University, US, have independently provided data on how TCA molecules bind to a bacterial analogue of a mammalian neurotransmitter transporter.

Antidepressants

Desipramine and clomipramine prevent the reuptake of monoamine neurotransmitters

Both groups of researchers used the leucine transporter protein from the bacterium Aquifex aeolicus, which is similar to human neurotransmitter transporters. Zhou's team crystallized the protein while it was bound to the TCA desipramine; Gouaux's group used clomipramine.

Structural crystallography data on the complexes revealed that the drugs occupy a cavity, referred to as an extracellular vestibule, within the transporter protein adjacent to the point where the substrate - in this case leucine - binds. Once docked into the cavity, the TCA molecule forms ionic bonds with the protein and induces subtle structural alterations that effectively close the 'gate' that would allow the leucine to vacate the protein. With the substrate locked in place, the transporter cannot do its job. 

'By directly locking the gate, desipramine prevents conformational changes and blocks substrate transport,' Zhou's team report.

Clomipramine in situ

Clomipramine nestles inside a complex protein

© Nature

Sarah Bailey, a pharmacologist at the University of Bath, UK, told Chemistry World, 'Most prescribed antidepressants act by blocking neurotransmitter reuptake transporter proteins. Understanding the precise interaction between antidepressant drugs and the chemical structure of the transporter will enable the development of more selective, more effective drugs and reduce unwanted side effects.'

'These papers describe for the first time the mechanism by which antidepressants are likely to block reuptake of neurotransmitters at specific transporters, such as the serotonin transporter,' said Katherine Aitchison, of the Institute of Psychiatry at King's College London.

'A well-known antidepressant is fluoxetine, also known as Prozac. This is termed a selective serotonin reuptake inhibitor (SSRI) because it inhibits uptake of serotonin by the serotonin transporter back into a neurone,' Aitchison added. 'However, exactly how it inhibits the uptake of serotonin has not previously been known. Now we know. This may help companies design new antidepressants and other drugs that work on these transporters, for the treatment of a variety of mental health problems including depression.'

Simon Hadlington

 

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References

1 Z Zhou et al., Science, 2007, DOI: 10.1126/science.1147614

2 SK Singh et al., Nature, 2007, DOI: 10.1038/nature.06038

Also of interest

BBC and GSK battle over Seroxat

Antidepressant under spotlight once again

The effects, if any, of antidepressants

Recent reports that the most popularly prescribed class of antidepressants.

Related Links

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