(Q28378301)

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Selective antagonism by naloxonazine of antinociception by Tyr-D-Arg-Phe-beta-Ala, a novel dermorphin analogue with high affinity at mu-opioid receptors

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Selective antagonism by naloxonazine of antinociception by Tyr-D-Arg-Phe-beta-Ala, a novel dermorphin analogue with high affinity at mu-opioid receptors (English)

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object named as

S Takeda

2

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author name string

S Sakurada

1

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T Sato

3

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T Hayashi

4

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M Yuki

5

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M Kutsuwa

6

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K Tan-No

7

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C Sakurada

8

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K Kisara

9

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T Sakurada

10

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language of work or name

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publication date

28 April 2000

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European Journal of Pharmacology

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395

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2

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107-12

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Pharmacological data on dermorphins, a new class of potent opioid peptides from amphibian skin

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3-Methoxynaltrexone, a selective heroin/morphine-6beta-glucuronide antagonist

1 reference

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N-terminal tetrapeptide of dermorphin and D-Arg-substituted tetrapeptides: inactivation process of the antinociceptive activity by peptidase

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Comparison of the antinociceptive effects of new [D-Arg2]-dermorphin tetrapeptide analogs and morphine in mice

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Structure-activity relationships of dermorphin synthetic analogues

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Characterisation of mu-opioid receptors on SH-SY5Y cells using naloxonazine and beta-funaltrexamine

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Intrathecal morphine in mice: a new technique

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Characterization of dermorphin binding to membranes of rat brain and heart

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Naloxonazine actions in vivo

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Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene

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Pharmacological mechanisms of opioid analgesics.

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Different mu receptor subtypes mediate spinal and supraspinal analgesia in mice.

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Comparison of naloxonazine and β-funaltrexamine antagonism of μ1 and μ2 opioid actions

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Differential involvement of mu-opioid receptor subtypes in endomorphin-1- and -2-induced antinociception

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Studies on analgesic oligopeptides. VII. Solid phase synthesis and biological properties of Tyr-D-Arg-Phe-beta Ala-NH2 and its fluorinated aromatic amino acid derivatives

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Contribution of spinal mu1-opioid receptors to morphine-induced antinociception

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Retention of heroin and morphine-6 beta-glucuronide analgesia in a new line of mice lacking exon 1 of MOR-1.

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Spinal action of dermorphin, an extremely potent opioid peptide from frog skin

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Cloning and expression of an isoform of the rat mu opioid receptor (rMOR1B) which differs in agonist induced desensitization from rMOR1.

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Synthesis and pharmacological activity of dermorphin and its N-terminal sequences

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Identifiers

10.1016/S0014-2999(00)00166-7

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