The κ-Opioid Receptor Agonist U-50488 Blocks Ca2+ Channels in a Voltage- and G Protein–Independent Manner in Sensory Neurons
Author:
Publisher
BMJ
Subject
Anesthesiology and Pain Medicine,General Medicine
Reference24 articles.
1. Opioid Pharmacology
2. Disruption of the kappa -opioid receptor gene in mice enhances sensitivity to chemical visceral pain, impairs pharmacological actions of the selective kappa -agonist U-50,488H and attenuates morphine withdrawal
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4. Multiple sodium channels and their roles in electrogenesis within dorsal root ganglion neurons
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