Inhibition of M-current in cultured rat superior cervical ganglia by linopirdine: Mechanism of action studies
- 1 November 1997
- journal article
- Published by Elsevier in Neuropharmacology
- Vol. 36 (11-12) , 1747-1753
- https://doi.org/10.1016/s0028-3908(97)00155-x
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Pharmacology of the Neurotransmitter Release Enhancer Linopirdine (DuP 996), and Insights into Its Mechanism of ActionPublished by Elsevier ,1996
- Reduction of spike frequency adaptation and blockade of M‐current in rat CA1 pyramidal neurones by linopirdine (DuP 996), a neurotransmitter release enhancerBritish Journal of Pharmacology, 1995
- Muscarinic M-current inhibition via G alpha q/11 and alpha-adrenoceptor inhibition of Ca2+ current via G alpha o in rat sympathetic neurones.The Journal of Physiology, 1994
- Myosin light chain kinase occurs in bullfrog sympathetic neurons and may modulate voltage-dependent potassium currentsNeuron, 1993
- On the transduction mechanism for muscarine‐induced inhibition of M‐current in cultured rat sympathetic neurones.The Journal of Physiology, 1989
- Stimulation of phosphatidylinositol (PI) turnover may mediate the muscarinic suppression of the M-current in hippocampal pyramidal cellsNeuroscience Letters, 1988
- M-currents: an updateTrends in Neurosciences, 1988
- Effects of phorbol dibutyrate on M currents and M current inhibition in bullfrog sympathetic neuronsCellular and Molecular Neurobiology, 1987
- Pharmacological inhibition of the M‐currentThe Journal of Physiology, 1982
- Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patchesPflügers Archiv - European Journal of Physiology, 1981