نتایج جستجو برای: oral desensitization

تعداد نتایج: 259564  

Journal: :Molecular pharmacology 2012
Seksiri Arttamangkul Elaine K Lau Hsin-Wei Lu John T Williams

The phosphorylation of μ-opioid receptors (MOPRs) by G protein-coupled receptor kinases (GRKs), followed by arrestin binding, is thought to be a key pathway leading to desensitization and internalization. The present study used the combination of intracellular and whole-cell recordings from rats and mice, as well as live cell imaging of Flag-tagged MOPRs from mouse locus ceruleus neurons, to ex...

2014
Lisa Adelfinger Rostislav Turecek Klara Ivankova Anders A. Jensen Stephen J. Moss Martin Gassmann Bernhard Bettler

GABAB receptors assemble from GABAB1 and GABAB2 subunits. GABAB2 additionally associates with auxiliary KCTD subunits (named after their K(+) channel tetramerization-domain). GABAB receptors couple to heterotrimeric G-proteins and activate inwardly-rectifying K(+) channels through the βγ subunits released from the G-protein. Receptor-activated K(+) currents desensitize in the sustained presence...

Journal: :Molecular pharmacology 2008
Michael S Virk John T Williams

Agonist-selective actions of opioids on the desensitization of mu-opioid receptors (MORs) have been well characterized, but few if any studies have examined agonist-dependent recovery from desensitization. The outward potassium current induced by several opioids was studied using whole-cell voltage-clamp recordings in locus ceruleus neurons. A brief application of the irreversible opioid antago...

2015
Janet D. Lowe Helen S. Sanderson Alexandra E. Cooke Mehrnoosh Ostovar Elena Tsisanova Sarah L. Withey Charles Chavkin Stephen M. Husbands Eamonn Kelly Graeme Henderson Chris P. Bailey

There is ongoing debate about the role of G protein–coupled receptor kinases (GRKs) in agonist-induced desensitization of the m-opioid receptor (MOPr) in brain neurons. In the present paper, we have used a novel membrane-permeable, small-molecule inhibitor of GRK2 and GRK3, Takeda compound 101 (Cmpd101; 3-[[[4-methyl-5-(4-pyridyl)-4H-1,2,4-triazole-3-yl] methyl] amino]N-[2-(trifuoromethyl) benz...

Journal: :Koomesh 2021

Effect of eye movement desensitization and reprocessing on death anxiety gastrointestinal cancer patients in Qazvin hospital 2018: A randomized clinical trial

Journal: :Armaghane Danesh Bimonthly Journal 2022

The Effect of Eye Movement Desensitization and Reprocessing on Pain Intensity in Cancer Patients (24-Month Follow-Up)

Journal: :The Journal of General Physiology 1977
B Scubon-Mulieri R L Parsons

The time course of carbachol-induced desensitization onset and recovery of sensitivity after desenitization have been compared at the frog neuromuscular junction. The activation-desensitization sequence was determined from input conductance measurements using potassium-depolarized muscle preparations. Both desensitization onset and recovery from desensitization could be adequately described by ...

Journal: :Journal of neural engineering 2011
Daniel K Freeman Shelley I Fried

Retinal prostheses aim to restore functional vision to those blinded by outer retinal diseases using electric stimulation of surviving neurons. Previous work indicates that repetitive stimulation with stimuli that activate the synaptic network reduces the sensitivity of retinal neurons to further stimulation. Such desensitization may contribute to the fading of visual percepts over time reporte...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2009
Vu C Dang Ian A Napier MacDonald J Christie

Sustained stimulation of G-protein coupled receptors (GPCRs) leads to rapid loss of receptor function (acute desensitization). For many GPCRs including the mu-opioid receptor (MOR), an accepted mechanism for acute desensitization is through G-protein coupled receptor kinase (GRKs) mediated phosphorylation of the receptor, which facilitates the binding of beta-arrestins (betaarrs) to the recepto...

Journal: :Anesthesiology 1999
D E Raines V T Zachariah

BACKGROUND The nAcChoR is the prototypical member of a superfamily of ligand-gated ion channels that are all relevant targets of anesthetics and undergo desensitization upon prolonged exposure to agonist. This study was designed to investigate the effects of representative normal alcohols on the apparent rate of acetylcholine-induced nAcChoR desensitization. METHODS Nicotinic acetylcholine re...

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