Preliminary noteProglumide selectively potentiates supraspinal μ1 opioid analgesia in mice
References (10)
- et al.
Enhancement of morphine analgesia and prevention of morphine tolerance in the rat by the CCK antagonist, L-364,718
Eur. J. Pharmacol.
(1988) - et al.
Potentiation of beta-endorphin effects by proglumide in rats
Eur. J. Pharmacol.
(1985) - et al.
Dissociation of tolerance and dependence to morphine: a possible role for cholecystokinin
Brain Res.
(1987) - et al.
Multiple mu opiate receptors
Life Sci.
(1986) - et al.
Different mu receptor subtypes mediate spinal an supraspinal analgesia in mice
Eur. J. Pharmacol.
(1989)
There are more references available in the full text version of this article.
Cited by (10)
CCK antagonists: Pharmacology and therapeutic interest
1994, Pharmacology and TherapeuticsInteractive Mechanisms of Supraspinal Sites of Opioid Analgesic Action: A Festschrift to Dr. Gavril W. Pasternak
2021, Cellular and Molecular NeurobiologyMu opioids and their receptors: Evolution of a concept
2013, Pharmacological ReviewsPain Management: Expanding the Pharmacological Options
2009, Pain Management: Expanding the Pharmacological Options
Copyright © 1990 Published by Elsevier Ltd.