Morphine decreases the voltage sensitivity of slow sodium channels |
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Authors: | B. V. Krylov A. V. Derbenev S. A. Podzorova M. I. Lyudyno A. V. Kuz'min N. L. Izvarina |
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Affiliation: | (1) Excitable Membrane Physiology Section, I. P. Pavlov Institute of Physiology, Russian Academy of Scences, 6 Makarov Embankment, 199034 St. Petersburg, Russia;(2) Kuban State University, 149 Stavropolskaya, 350040 Krasnodar, Russia;(3) Institute of Pharmacology, I. P. Pavlov Medical Academy, 6/8 L. Tolstoy Street, 197089 St. Petersburg, Russia |
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Abstract: | Cell membrane recordings were made in conditions of voltage clamping with tight attachment of the microelectrode—patch clamping— to study the effects of morphine on tetrodotoxin-resistant (TTXr) sodium channels in rat spinal ganglion neurons in culture. The effects of a number of biologically active substances which regulate the receptor-mediated actions of morphine were studied. The effects of morphine were found to involve a chain of sequential reactions leading to decreases in the transfer of effective charge (Zeff) by the activatory gate system of TTXr sodium channels, depending on the concentration of agonist in the extracellular solution. A value of 8 nM was obtained forK D , with a Hill coefficient of X=0.5. Non-specific antagonists of opioid receptors blocked the actions of morphine; these included ouabain at a concentration of 100 μM. An inhibitor, and activator, and a blocker of G-proteins had no effect on the effective charge. These data provide evidence that morphine decreases the voltage sensitivity of TTXr sodium channels. Translated from Rossiiskii Fiziologicheskii Zhurnal imeni I. M. Sechenova, Vol. 85, No. 2, pp. 225–236, February, 1999. |
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Keywords: | Spinal ganglion neurons TTXr sodium channels Na+,K+-ATPase opioid receptors |
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