κ-opioid receptor mediated antinociception in rats is dependent on the functional state of dihydropyridine-sensitive calcium channels
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience
Reference34 articles.
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1. Spider Venom Peptide Pn3a Inhibition of Primary Afferent High Voltage-Activated Calcium Channels;Frontiers in Pharmacology;2021-01-28
2. Peripheral antinociception induced by δ-opioid receptors activation, but not μ- or κ-, is mediated by Ca2+-activated Cl− channels;European Journal of Pharmacology;2012-01
3. In vivo evaluation of (+)-MR200 as a new selective sigma ligand modulating MOP, DOP and KOP supraspinal analgesia;Life Sciences;2006-04
4. L-type Ca2+ channel modulation by dihydropyridines potentiates κ-opioid receptor agonist induced acute analgesia and inhibits development of tolerance in rats;Neuropharmacology;2002-03
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