A novel muscarinic receptor-independent mechanism of KCNQ2/3 potassium channel blockade by Oxotremorine-M
Author:
Funder
Eli Lilly and Company, United States
Publisher
Elsevier BV
Subject
Pharmacology
Reference27 articles.
1. Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone;Brown;Nature,1980
2. M1-like muscarinic acetylcholine receptors regulate fast-spiking interneuron excitability in rat dentate gyrus;Chiang;Neuroscience,2010
3. M-currents in voltage clamped mammalian sympathetic neurones;Constanti;Neurosci. Lett.,1981
4. Types of muscarinic response in Xenopus oocytes;Dascal;Life Sci.,1980
5. Xenopus oocyte resting potential, muscarinic responses and the role of calcium and guanosine 3′,5′-cyclic monophosphate;Dascal;J. Physiol.,1984
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1. Muscarinic modulation of M and h currents in gerbil spherical bushy cells;PLOS ONE;2020-01-15
2. Identification and pharmacological profile of SPP1, a potent, functionally selective and brain penetrant agonist at muscarinic M1 receptors;British Journal of Pharmacology;2018-11-16
3. A mechanistic review on GNAO1-associated movement disorder;Neurobiology of Disease;2018-08
4. Oxotremorine-M potentiates NMDA receptors by muscarinic receptor dependent and independent mechanisms;Biochemical and Biophysical Research Communications;2018-01
5. KCNQ2/3/5 channels in dorsal root ganglion neurons can be therapeutic targets of neuropathic pain in diabetic rats;Molecular Pain;2018-01
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