Comparison of the Novel Subtype-Selective GABAA Receptor-Positive Allosteric Modulator NS11394 [3′-[5-(1-Hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile] with Diazepam, Zolpidem, Bretazenil, and Gaboxadol in Rat Models of Inflammatory and Neuropathic Pain-Reference-Cited by-同舟云学术

Comparison of the Novel Subtype-Selective GABAA Receptor-Positive Allosteric Modulator NS11394 [3′-[5-(1-Hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile] with Diazepam, Zolpidem, Bretazenil, and Gaboxadol in Rat Models of Inflammatory and Neuropathic Pain

Published:2008-09-12 Issue:3 Volume:327 Page:969-981
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Munro G.,Lopez-Garcia J. A.,Rivera-Arconada I.,Erichsen H. K.,Nielsen E. Ø.,Larsen J. S.,Ahring P. K.,Mirza N. R.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference42 articles.

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2. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man

3. Laminar compartmentalization of GABAA-receptor subtypes in the spinal cord: an immunohistochemical study

4. Complex changes of GABAA and GABAB receptor binding in the spinal cord dorsal horn following peripheral inflammation or neurectomy

5. GABA decreases in the spinal cord dorsal horn after peripheral neurectomy

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