INT29356
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
The results of these studies have allowed the identification of a low energy conformer common to all of these analogs which could be responsible for their high affinity delta-receptor binding. | |||||||||||||||
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Sodium ions increase the binding of the antagonist peptide ICI 174864 to the delta-opiate receptor. | |||||||||||||||
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Here we report that endocytosis of mu and delta opioid receptors is not required for efficient ligand-induced activation of mitogen-activated protein kinase. | |||||||||||||||
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Replacement of Phe(3) by Dmp increased the affinity over 10-fold for both mu- and delta-opioid receptors, without affecting receptor selectivity. | |||||||||||||||
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Naltrexone disrupts this feedback control by reducing micro opioid receptor function, thereby up-regulating delta opioid receptor binding, which results in an enhanced NK cell cytolytic response to delta opioid receptor ligands. | |||||||||||||||
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Staggered expression resulted in non-interacting mu and delta receptors, even though both receptors were colocalized at the cell surface. | |||||||||||||||
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Structural requirements for delta opioid receptor binding. | |||||||||||||||
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Similarly, treatment with mu-selective ligands results in a significant increase in the binding of a delta receptor agonist. | |||||||||||||||
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General Comments
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