Selective stabilization of the intermediate inactivated Na+ channel by the new-generation anticonvulsant rufinamide-Reference-Cited by-同舟云学术

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Selective stabilization of the intermediate inactivated Na+ channel by the new-generation anticonvulsant rufinamide

Published:2022-03 Issue: Volume:197 Page:114928
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Lin Yun-Chu,Lai Yi-Chen,Lin Tien-Hung,Yang Ya-Chin,Kuo Chung-Chin

Funder

Taiwan Ministry of Science and Technology

Chang Gung Medical Foundation

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference53 articles.

1. Inactivation of the sodium channel. II. Gating current experiments;Armstrong;J. Gen. Physiol.,1977

2. Rufinamide;Arroyo;Neurotherapeutic,2007

3. External pore residue mediates slow inactivation in µ1 rat skeletal muscle sodium channels;Balser;J. Physiol.,1996

4. Nitrendipine block of cardiac calcium channels: high-affinity binding to the inactivated state;Bean;Proc. Natl. Acad. Sci. U.S.A.,1984

5. Molecular dynamics of the sodium channel pore vary with gating: interactions between P-segment motions and inactivation;Bénitah;J. Neurosci.,1999

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Persistent sodium currents in neurons: potential mechanisms and pharmacological blockers;Pflügers Archiv - European Journal of Physiology;2024-07-05

2. Inhibition of resurgent Na+ currents by rufinamide;Neuropharmacology;2024-04

3. Rufinamide, a Triazole-Derived Antiepileptic Drug, Stimulates Ca2+-Activated K+ Currents While Inhibiting Voltage-Gated Na+ Currents;International Journal of Molecular Sciences;2022-11-08

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