Inhibition of Na{sup +} channel currents in rat myoblasts by 4-aminopyridine
- Center for Brain Science Research, School of Life Sciences, Fudan University, Shanghai 200433 (China)
Our previous study revealed that 4-aminopyridine (4-AP), a specific blocker of A-type current, could also inhibit inward Na{sup +} currents (I {sub Na}) with a state-independent mechanism in rat cerebellar granule cells. In the present study, we report an inhibitory effect of 4-AP on voltage-gated and tetrodotoxin (TTX)-sensitive I {sub Na} recorded from cultured rat myoblasts. 4-AP inhibited I {sub Na} amplitude in a dose-dependent manner between the concentrations of 0.5 and 10 mM without significant alteration in the activation or inactivation kinetics of the channel. By comparison to the 4-AP-induced inhibitory effect on cerebellum neurons, the inhibitory effect on myoblasts was enhanced through repetitive pulse and inflected by changing frequency. Specifically, the lower the frequency of pulse, the higher the inhibition observed, suggesting that block manner is inversely use-dependent. Moreover, experiments adding 4-AP to the intracellular solution indicate that the inhibitory effects are localized inside the cell. Additionally, 4-AP significantly modifies the properties of steady-state activation and inactivation kinetics of the channel. Our data suggest that the K{sup +} channel blocker 4-AP inhibits both neuron and myoblast Na{sup +} channels via different mechanisms. These findings may also provide information regarding 4-AP-induced pharmacological and toxicological effects in clinical use and experimental research.
- OSTI ID:
- 20722000
- Journal Information:
- Toxicology and Applied Pharmacology, Vol. 207, Issue 3; Other Information: DOI: 10.1016/j.taap.2005.01.009; PII: S0041-008X(05)00029-3; Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0041-008X
- Country of Publication:
- United States
- Language:
- English
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