Contrasting Neurochemical Interactions of Tiletamine, a Potent Phencyclidine (PCP) Receptor Ligand, with the N-Methyl-D-Aspartate-Coupled and -Uncoupled PCP Recognition Sites-Reference-Cited by-同舟云学术

Contrasting Neurochemical Interactions of Tiletamine, a Potent Phencyclidine (PCP) Receptor Ligand, with the N-Methyl-D-Aspartate-Coupled and -Uncoupled PCP Recognition Sites

Published:1991-03 Issue:3 Volume:56 Page:890-897
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J Neurochem

Author:

Rao Tadimeti S.,Contreras Patricia C.,Cler Julie A.,Mick Steve J.,Dilworth Vickie M.,Iyengar Smriti,Monahan Joseph B.,Wood Paul L.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.1991.tb02005.x/fullpdf

Reference36 articles.

1. The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N-methyl-aspartate

2. A comparison of PCP-like compounds for NMDA antagonism in two models

3. Characterization of the binding of 3H-SCH 23390, a selective D-1 receptor antagonist ligand, in rat striatum

4. The N-methyl-D-aspartate antagonist, 2-amino-7-phosphonoheptanoate, produces phencyclidine-like behavioral effects in rats

5. Effect of several dopaminergic drugs and trihexyphenidyl on cholinergic parameters in the rat striatum

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