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Reply to Wang and Sadée.

作者信息

Henderson Graeme, Bullmore Edward T

机构信息

School of Physiology & Pharmacology, University of Bristol, Bristol, UK,

出版信息

Psychopharmacology (Berl). 2015 Apr;232(8):1495-6. doi: 10.1007/s00213-015-3900-7. Epub 2015 Mar 11.

DOI:10.1007/s00213-015-3900-7

PMID:25757674

Abstract

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本文引用的文献

The opioid receptor pharmacology of GSK1521498 compared to other ligands with differential effects on compulsive reward-related behaviours.

Psychopharmacology (Berl). 2015 Jan;232(1):305-14. doi: 10.1007/s00213-014-3666-3. Epub 2014 Jun 29.

Constitutively active μ-opioid receptors.

Methods Enzymol. 2010;484:445-69. doi: 10.1016/B978-0-12-381298-8.00022-8.

Identification of a novel "almost neutral" micro-opioid receptor antagonist in CHO cells expressing the cloned human mu-opioid receptor.

Synapse. 2010 Apr;64(4):280-8. doi: 10.1002/syn.20723.

In vivo characterization of 6beta-naltrexol, an opioid ligand with less inverse agonist activity compared with naltrexone and naloxone in opioid-dependent mice.

J Pharmacol Exp Ther. 2005 Jun;313(3):1150-62. doi: 10.1124/jpet.104.082966. Epub 2005 Feb 16.

Basal signaling activity of mu opioid receptor in mouse brain: role in narcotic dependence.

J Pharmacol Exp Ther. 2004 Feb;308(2):512-20. doi: 10.1124/jpet.103.054049. Epub 2003 Nov 4.

Inverse agonists and neutral antagonists at mu opioid receptor (MOR): possible role of basal receptor signaling in narcotic dependence.

J Neurochem. 2001 Jun;77(6):1590-600. doi: 10.1046/j.1471-4159.2001.00362.x.

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Reply to Wang and Sadée.

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