Brain passage of BUBU, a highly selective and potent agonist for δ opioid receptors: In vivo binding and μ versus δ receptors occupancy

Author:

Delay-Goyet Philippe,Ruiz-Gayo Mariano,Baamonde Ana,Gacel Gilles,Morgat Jean-Louis,Roques Bernard P.

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Biological Psychiatry,Clinical Biochemistry,Pharmacology,Toxicology,Biochemistry

Reference48 articles.

1. Baamonde, A.; Daugé, V.; Gacel, G.; Roques, B. P. Systemic administration of BUBU, a highly selective δ opioid agonist, induces μ receptor mediated analgesia in mice. J. Pharmacol. Exp. Ther.; submitted.

2. Enhancement of blood-brain barrier permeability to sodium fluorescein by stimulation of μ opioid receptors in mice;Baba;Naunyn Schmiedebergs Arch. Pharmacol.,1988

3. Neuropeptides and the blood-brain barrier;Begley,1986

4. Differential depressive action of two μ and ∂ opioid ligands on neuronal responses to noxious stimuli in the thalamic ventrobasal complex of rat;Benoist;Brain Res.,1986

5. Metkephamid (Tyr-D-Ala-Gly-Phe-N(Me)Met-NH2), a potent opioid peptide: Receptor binding and analgesic properties;Burkhardt;Peptides,1982

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