Mu opioid receptor regulation and opiate responsiveness. - Wikidata - awgldk - TriplyDB

Mu opioid receptor regulation and opiate responsiveness.

Mu opioid receptor regulation and opiate responsiveness.

http://www.wikidata.org/entity/Q36341679

about

Interaction of the mu-opioid receptor with GPR177 (Wntless) inhibits Wnt secretion: potential implications for opioid dependence MOR is not enough: identification of novel mu-opioid receptor interacting proteins using traditional and modified membrane yeast two-hybrid screens Effects of opiates and HIV proteins on neurons: the role of ferritin heavy chain and a potential for synergism Co-activation of μ- and δ-opioid receptors elicits tolerance to morphine-induced ventilatory depression via generation of peroxynitrite A novel type of glial cell in the retina is stimulated by insulin-like growth factor 1 and may exacerbate damage to neurons and Müller glia.Contribution of mu and delta opioid receptors to the pharmacological profile of kappa opioid receptor subtypes.Targeting TRPV1 as an alternative approach to narcotic analgesics to treat chronic pain conditions.Single and repeated ultra-rapid detoxification prevents cognitive impairment in morphine addicted rats: a privilege for single detoxification.Inhibition of microglial P2X4 receptors attenuates morphine tolerance, Iba1, GFAP and mu opioid receptor protein expression while enhancing perivascular microglial ED2.Ultrastructural relationship between the mu opioid receptor and its interacting protein, GPR177, in striatal neurons.An opioid agonist that does not induce mu-opioid receptor--arrestin interactions or receptor internalization.Predictors of buprenorphine initial outpatient maintenance and dose taper response among non-treatment-seeking heroin dependent volunteers Reduction in cerebral perfusion after heroin administration: a resting state arterial spin labeling study.Functional selectivity at the μ-opioid receptor: implications for understanding opioid analgesia and tolerance.Chronic methadone treatment shows a better cost/benefit ratio than chronic morphine in mice.Modulation of gastrointestinal function by MuDelta, a mixed µ opioid receptor agonist/ µ opioid receptor antagonist.Genetic and Non-genetic Factors Associated With Constipation in Cancer Patients Receiving Opioids.Morphine inhibits sleep-promoting neurons in the ventrolateral preoptic area via mu receptors and induces wakefulness in rats Morphine: a protective or destructive role in neurons?Synthesis, modeling, and pharmacological evaluation of UMB 425, a mixed μ agonist/δ antagonist opioid analgesic with reduced tolerance liabilities.What do plasma beta-endorphin levels reveal about endogenous opioid analgesic function?Development of functionally selective, small molecule agonists at kappa opioid receptors.Opioids in chronic non-cancer pain.Changing mechanisms of opiate tolerance and withdrawal during early development: animal models of the human experience.RGS9-2 Modulates Responses to Oxycodone in Pain-Free and Chronic Pain States.RGS9-2 modulates nociceptive behaviour and opioid-mediated synaptic transmission in the spinal dorsal horn.Poorly controlled postoperative pain: prevalence, consequences, and prevention.Absence of μ opioid receptor mRNA expression in astrocytes and microglia of rat spinal cord Brain region specific actions of regulator of G protein signaling 4 oppose morphine reward and dependence but promote analgesia.Clinical cases in acute intoxication.Live cell monitoring of mu-opioid receptor-mediated G-protein activation reveals strong biological activity of close morphine biosynthetic precursors.Chronic intermittent hypoxia decreases pain sensitivity and increases the expression of HIF1α and opioid receptors in experimental rats.Bias Factor and Therapeutic Window Correlate to Predict Safer Opioid Analgesics.Intravenous morphine can avoid distressing constipation associated with oral morphine: a retrospective analysis of our experience in 11 patients in the palliative care in-patient unit.A randomized, Phase IIb study investigating oliceridine (TRV130), a novel µ-receptor G-protein pathway selective (μ-GPS) modulator, for the management of moderate to severe acute pain following abdominoplasty.The Effect of Trimebutine on the Overlap Syndrome Model of Guinea Pigs

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Mu opioid receptor regulation and opiate responsiveness.

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2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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2005年學術文章

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Mu opioid receptor regulation and opiate responsiveness.

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Mu opioid receptor regulation and opiate responsiveness.

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Mu opioid receptor regulation and opiate responsiveness.

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Mu opioid receptor regulation and opiate responsiveness.

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Mu opioid receptor regulation and opiate responsiveness.

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The AAPS Journal

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Mu opioid receptor regulation and opiate responsiveness.

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Kirsten M Raehal

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P2860

Beta-arrestin-dependent formation of beta2 adrenergic receptor-Src protein kinase complexes

beta-arrestin-dependent endocytosis of proteinase-activated receptor 2 is required for intracellular targeting of activated ERK1/2

beta-Arrestin: a protein that regulates beta-adrenergic receptor function

G-protein-coupled receptor heterodimerization modulates receptor function

Activation and targeting of extracellular signal-regulated kinases by beta-arrestin scaffolds

Beta-arrestin 2: a receptor-regulated MAPK scaffold for the activation of JNK3

beta-arrestin1 interacts with the catalytic domain of the tyrosine kinase c-SRC. Role of beta-arrestin1-dependent targeting of c-SRC in receptor endocytosis

Regulation of tyrosine kinase activation and granule release through beta-arrestin by CXCRI

Regulation of receptor fate by ubiquitination of activated beta 2-adrenergic receptor and beta-arrestin

Oligomerization of opioid receptors with beta 2-adrenergic receptors: a role in trafficking and mitogen-activated protein kinase activation

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