Results 241 to 250 of about 18,176 (269)

κ-Opioid Receptor Modulation of GABAergic Inputs onto Ventrolateral Periaqueductal Gray Dopamine Neurons. [PDF]

Mol Neuropsychiatry, 2019
Li C, Kash TL.
europepmc   +1 more source

Human Peripheral Blood Mononuclear Cells Express Nociceptin/Orphanin FQ, but Not μ, δ, or κ Opioid Receptors

, 2007
John P. Williams, Jonathan P. Thompson, John McDonald, Timothy Barnes, Tom Cote, David J. Rowbotham, David G. Lambert   +6 more
openalex   +1 more source

G protein signaling-biased agonism at the κ-opioid receptor is maintained in striatal neurons. [PDF]

Sci Signal, 2018
Ho JH, Stahl EL, Schmid CL, Scarry SM, Aubé J, Bohn LM.   +5 more
europepmc   +1 more source

κ-Opioid receptor stimulation reduces palmitate-induced apoptosis via Akt/eNOS signaling pathway. [PDF]

Lipids Health Dis, 2019
Cui Y, Feng N, Gu X, Fu F, Li J, Guo H, Liu Y, Zhang S, Li J, Wang Y, Jia M, Yang L, Zhang F, Wang Y, Fan R, Pei J.   +15 more
europepmc   +1 more source

Development and In Vivo Evaluation of a κ-Opioid Receptor Agonist as a PET Radiotracer with Superior Imaging Characteristics. [PDF]

J Nucl Med, 2019
Li S, Zheng MQ, Naganawa M, Kim S, Gao H, Kapinos M, Labaree D, Huang Y.   +7 more
europepmc   +1 more source

Negative modulation of spinal κ-opioid receptor-mediated antinociception by the µ-opioid receptor at selective doses of (-)-pentazocine. [PDF]

Neuroreport, 2018
Robinson DL, Nag S, Mokha SS.
europepmc   +1 more source

Hypertensive state, independent of hypertrophy, exhibits an attenuated decrease in systolic function on cardiac κ-opioid receptor stimulation

, 2009
Craig Bolte, Gilbert Newman, Jo El J. Schultz   +2 more
openalex   +2 more sources

Design, Synthesis and Pharmacological Evaluation of Novel Endomorphin Analogues with Multiple Structural Modifications [PDF]

, 2012
Mallareddy Jayapal Reddy
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Review of the potential health impact of ß-casomorphins and related peptides: Report of the DATEX Working Group on ß-casomorphins [PDF]

FitzGerald, R.J., Korhonen, H.J.T., Livesey, C.T., Noni, I., De, Roux, Y., Le, Thorsdottir, I., Tomé, D., Witkamp, R.F.   +7 more
core  

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Mechanism of direct Cav2.2 channel block by the κ-opioid receptor agonist U50488H

Neuropharmacology, 2016
U50488H is a benzeneacetamide κ-opioid receptor (κ-OR) agonist analgesic, widely used for investigating the pharmacology of G protein-coupled κ-ORs. However, U50488H is also known to directly block various voltage-gated ion channels in a G protein-independent manner.
Berecki, Géza, Motin, Leonid, Adams, David J   +2 more
openaire   +4 more sources