Morphine-activated opioid receptors elude desensitization by beta-arrestin.
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Morphine induces endocytosis of neuronal mu-opioid receptors through the sustained transfer of Galpha subunits to RGSZ2 proteinsRegulation of mu opioid receptor internalization by the scaffold protein RanBPMA heterodimer-selective agonist shows in vivo relevance of G protein-coupled receptor dimers.Beta-arrestin-dependent mu-opioid receptor-activated extracellular signal-regulated kinases (ERKs) Translocate to Nucleus in Contrast to G protein-dependent ERK activationMorphine-induced physiological and behavioral responses in mice lacking G protein-coupled receptor kinase 6The analgesic efficacy of fentanyl: relationship to tolerance and mu-opioid receptor regulationEssential role for RGS9 in opiate actionNeurokinin 1 receptors regulate morphine-induced endocytosis and desensitization of mu-opioid receptors in CNS neuronsMultiple endocytic pathways of G protein-coupled receptors delineated by GIT1 sensitivityThe emerging roles of β-arrestins in fibrotic diseasesHeterologous activation of protein kinase C stimulates phosphorylation of delta-opioid receptor at serine 344, resulting in beta-arrestin- and clathrin-mediated receptor internalizationBeta-arrestins: multifunctional cellular mediatorsMultiple actions of spinophilin regulate mu opioid receptor functionActivation of mu opioid receptors sensitizes transient receptor potential vanilloid type 1 (TRPV1) via β-arrestin-2-mediated cross-talkIdentification of the First Marine-Derived Opioid Receptor "Balanced" Agonist with a Signaling Profile That Resembles the EndorphinsProteasome involvement in agonist-induced down-regulation of mu and delta opioid receptors.High-affinity naloxone binding to filamin a prevents mu opioid receptor-Gs coupling underlying opioid tolerance and dependence.Brain region-specific N-glycosylation and lipid rafts association of the rat mu opioid receptorG-protein coupled receptor kinases as modulators of G-protein signalling.Agonist-dependent mu-opioid receptor signaling can lead to heterologous desensitization.beta-Arrestin2, interacting with phosphodiesterase 4, regulates synaptic release probability and presynaptic inhibition by opioids.Chronic ethanol consumption in rats produces opioid antinociceptive tolerance through inhibition of mu opioid receptor endocytosis.Mutational analysis of the structure and function of opioid receptors.Phosphorylation of EEA1 by p38 MAP kinase regulates mu opioid receptor endocytosis.Structure and regulation of opioid receptors.How to design an opioid drug that causes reduced tolerance and dependence.Receptors and transmission in the brain-gut axis: potential for novel therapies. III. Mu-opioid receptors in the enteric nervous system.The role of beta-arrestin2 in the severity of antinociceptive tolerance and physical dependence induced by different opioid pain therapeutics.Opioid-induced mitogen-activated protein kinase signaling in rat enteric neurons following chronic morphine treatment.Examining the role of mu opioid receptor endocytosis in the beneficial and side-effects of prolonged opioid use: from a symposium on new concepts in mu-opioid pharmacologyChronic morphine treatment attenuates cell growth of human BT474 breast cancer cells by rearrangement of the ErbB signalling network.Morphine induces μ opioid receptor endocytosis in guinea pig enteric neurons following prolonged receptor activationAn opioid agonist that does not induce mu-opioid receptor--arrestin interactions or receptor internalization.Opioid receptor desensitization: mechanisms and its link to toleranceFunctional selectivity and time-dependence of μ-opioid receptor desensitization at nerve terminals in the mouse ventral tegmental areaChange in functional selectivity of morphine with the development of antinociceptive tolerance.Heteromerization of the μ- and δ-opioid receptors produces ligand-biased antagonism and alters μ-receptor traffickingCo-expression of GRK2 reveals a novel conformational state of the µ-opioid receptorCholesterol regulates micro-opioid receptor-induced beta-arrestin 2 translocation to membrane lipid rafts.Effect of KEPI (Ppp1r14c) deletion on morphine analgesia and tolerance in mice of different genetic backgrounds: when a knockout is near a relevant quantitative trait locus.
P2860
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P2860
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@ast
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@en
type
label
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@ast
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@en
prefLabel
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@ast
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@en
P2860
P356
P1476
Morphine-activated opioid receptors elude desensitization by beta-arrestin.
@en
P2093
J L Whistler
M von Zastrow
P2860
P304
P356
10.1073/PNAS.95.17.9914
P407
P577
1998-08-01T00:00:00Z