Doxepin and imipramine but not fluoxetine reduce the activity of the rat glutamate transporter EAAT3 expressed in Xenopus oocytes-Reference-Cited by-同舟云学术

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Doxepin and imipramine but not fluoxetine reduce the activity of the rat glutamate transporter EAAT3 expressed in Xenopus oocytes

Published:2015-08-08 Issue:1 Volume:15 Page:
ISSN:1471-2253
Container-title:BMC Anesthesiology
language:en
Short-container-title:BMC Anesthesiol

Author:

Park Hye Jin,Baik Hee Jung,Kim Dong Yeon,Lee Guie Yong,Woo Jae Hee,Zuo Zhiyi,Chung Rack Kyung

Publisher

Springer Science and Business Media LLC

Subject

Anesthesiology and Pain Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12871-015-0098-5.pdf

Reference38 articles.

1. Danbolt NC. Glutamate uptake. Prog Neurobiol. 2001;65:1–105.

2. Kanai Y, Hediger MA. Primary structure and functional characterization of a high-affinity glutamate transporter. Nature. 1992;360:467–71.

3. Kanai Y, Smith CP, Hediger MA. A new family of neurotransmitter transporters: the high-affinity glutamate transporters. FASEB J. 1993;7:1450–9.

4. Maragakis NJ, Rothstein JD. Glutamate transporters in neurologic disease. Arch Neurol. 2001;58:365–70.

5. Nieoullon A, Canolle B, Masmejean F, Guillet B, Pisano P, Lortet S. The neuronal excitatory amino acid transporter EAAC1/EAAT3: does it represent a major actor at the brain excitatory synapse? J Neurochem. 2006;98:1007–18.

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