Monoamine transporter

From Wikipedia, the free encyclopedia

Monoamine transporters, as the name implies, transfer monoamine neurotransmitters in or out of a cell.

There are several different monoamine transporters:

• The dopamine transporter, DAT.
• The norepinephrine transporter, NET.
• The serotonin transporter, SERT.

DAT, NET and SERT are related to each other and they all consist of a structure of 12 transmembrane helices.

[edit] Drug action

Many drugs, such as antidepressants and psychoactives affect the monoamine transporters.

Modern antidepressants typically work by enhancing serotonergic, noradrenergic or dopaminergic neurotransmission by binding to the corresponding transporter, and thereby inhibiting neurotransmitter reuptake and raising active levels in the synapse. Examples include fluoxetine, a selective serotonin reuptake inhibitor; reboxetine, a norepinephrine reuptake inhibitor and bupropion, which inhibits both the norepinephrine and dopamine transporter.

The euphoric and addictive properties of amphetamine, methamphetamine and cocaine are thought to come from their potent DAT-blocking activity.

[edit] See also

• Glutamate transporter
• Vesicular monoamine transporter

[edit] References

G.E. Torres, R.R. Gainetdinov and M.G. Caron (2003). "Plasma membrane monoamine transporters: structure, regulation and function". Nat. Rev. Neurosci. 4 (1): 13-25. PMID 12511858. (Review)