Neurotransmitter transporter

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Neurotransmitter transporters are proteins that span cellular membranes and that serve to carry neurotransmitters across these membranes and to transport them to specific locations. There are more than twenty types of neurotransmitter transporters.[1] The transporters exist in the membranes of neurons and glia.

Vesicular transporters move neurotransmitters into synaptic vesicles, regulating the concentrations of substances within them.[2] Vesicular transporters rely on a proton gradient created by the hydrolysis of adenosine triphosphate (ATP) in order to carry out their work: vesicle ATPase hydrolyzes ATP, causing protons to be pumped into the vesicle and creating a proton gradient. Then the efflux of protons from the vesicle provides the energy to bring the neurotransmitter into the vesicle.[3]

Neurotransmitter transporters frequently use electrochemical gradients that exist across cell membranes to carry out their work. For example, some transporters use energy obtained by the cotransport of Na+ in order to move glutamate across membranes.

Normally, transporters in the synaptic membrane serve to remove neurotransmitters from the synaptic cleft and prevent their action or bring it to an end. However, on occasion transporters can work in reverse, transporting neurotransmitters into the synapse, allowing these neurotransmitters to bind to their receptors and exert their effect. This "nonvesicular release" of neurotransmitters is used by some cells, such as amacrine cells in the retina, as a normal form of neurotransmitter release.[4]

Types

Specific types of neurotransmitter transporters include the following:

Clinical significance

Antidepressants act by inhibiting norepinephrine and serotonin reuptake transporters.[1]

Cocaine exerts its effect by acting on the dopamine transporter.[1]

The antiepileptic drug tiagabine prevents the uptake of GABA by acting on the GABA transporter GAT-1.[1]

The expression of GABA transporter GAT-1 is decreased in the axonal cartridges of chandelier neurons in schizophrenia. [7]

See also

External links

References

  1. 1.0 1.1 1.2 1.3 Iversen L. 2000. Neurotransmitter transporters: fruitful targets for CNS drug discovery Mol Psychiatry Volume 5, Issue 4, Pages 357-362. Accessed January 8, 2007.
  2. Johnson J, Tian N, Caywood MS, Reimer RJ, Edwards RH, and Copenhagen DR. 2003. Vesicular Neurotransmitter Transporter Expression in Developing Postnatal Rodent Retina: GABA and Glycine Precede Glutamate. The Journal of Neuroscience. Volume 23, Issue 2, Pages 518-529. Accessed January 8, 2007.
  3. Kandel ER, Schwartz JH, Jessell TM. 2000. Principles of Neural Science, 4th ed., Page 287. McGraw-Hill, New York ISBN 0-8385-7701-6
  4. Kandel ER, Schwartz JH, Jessell TM. 2000. Principles of Neural Science, 4th ed., Page 295. McGraw-Hill, New York ISBN 0-8385-7701-6
  5. Broer A, Albers A, Setiawan I, Edwards RH, Chaudhry FA, Lang F, Wagner CA, and Broer S. 2002. Regulation of the glutamine transporter SN1 by extracellular pH and intracellular sodium ions. Journal of Physiology. Volume 15; Issue 539 (Pt 1), Pages 3-14. Accessed January 8, 2007.
  6. Weihe E, Tao-Cheng JH, Schäfer MK, Erickson JD, and Eiden LE. 1996. Visualization of the vesicular acetylcholine transporter in cholinergic nerve terminals and its targeting to a specific population of small synaptic vesicles. Proceedings of the National Academy of Sciences of the U.S.A. Volume 93, Issue 8, Pages 3547–3552. Accessed January 8, 2007.
  7. Volk D, Austin M, Pierri J, Sampson A, Lewis D. (2001) GABA transporter-1 mRNA in the prefrontal cortex in schizophrenia: decreased expression in a subset of neurons. Am J Psychiatry. 158(2):256-65. PMID 11156808 free fulltext article

External links


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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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