Effects of Agonists of μ-Opioid Receptors on P-Type Calcium Channels in Rat Purkinje Neurons
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology,General Neuroscience
Link
http://link.springer.com/content/pdf/10.1007/s11062-015-9505-2.pdf
Reference17 articles.
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3. V. Carabelli, I. Carra, and E. Carbone, “Localized secretion of ATP and opioids revealed through single Ca2+ channel modulation in bovine chromaffin cells,” Neuron, 20, 1255–1268 (1998).
4. T. Kanemasa, K. Asakura, and M. Ninomiya, “Kappaopioid agonist U50488 inhibits P-type Ca2+ channels by two mechanisms,” Brain Res., 702, 207–212 (1995).
5. V. A. Panchenko, O. A. Krishtal, F. Tegtmeier, and A. Y. Tsyndrenko, “R56865 as Ca(2+)-channel blocker in Purkinje neurons of rat: comparison with flunarizine and nimodipine,” Neuroscience, 54, 587–594 (1993).
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1. Mechanisms Underlying Positive Modulation of a Current through P-Type Calcium Channels in Purkinje Neurons by an Agonist of Opioid Receptors;Neurophysiology;2016-08
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