Effects of 4,9-anhydrotetrodotoxin on voltage-gated Na+ channels of mouse vas deferens myocytes and recombinant NaV1.6 channels-Reference-Cited by-同舟云学术

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Effects of 4,9-anhydrotetrodotoxin on voltage-gated Na+ channels of mouse vas deferens myocytes and recombinant NaV1.6 channels

Published:2018-02-16 Issue:5 Volume:391 Page:489-499
ISSN:0028-1298
Container-title:Naunyn-Schmiedeberg's Archives of Pharmacology
language:en
Short-container-title:Naunyn-Schmiedeberg's Arch Pharmacol

Author:

Takahara Kohei,Yamamoto Tadashi,Uchida Keiichiro,Zhu Hai-Lei,Shibata Atsushi,Inai Tetsuichiro,Noguchi Mitsuru,Yotsu-Yamashita Mari,Teramoto Noriyoshi

Funder

Japan Society for the Promotion of Science

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,General Medicine

Link

http://link.springer.com/article/10.1007/s00210-018-1476-6/fulltext.html

Reference19 articles.

1. Brackenbury WJ, Calhoun JD, Chen C, Miyazaki H, Nukina N, Oyama F, Ranscht B, Isom LL (2010) Functional reciprocity between Na+ channel NaV1.6 and beta1 subunits in the coordinated regulation of excitability and neurite outgrowth. Proc Natl Acad Sci U S A 107(5):2283–2288. https://doi.org/10.1073/pnas.0909434107

2. Catterall WA, Goldin AL, Waxman SG (2005) International union of pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels. Pharmacol Rev 57(4):397–409. https://doi.org/10.1124/pr.57.4.4

3. Clare JJ, Tate SN, Nobbs M, Romanos MA (2000) Voltage-gated sodium channels as therapeutic targets. Drug Discov Today 5(11):506–520. https://doi.org/10.1016/S1359-6446(00)01570-1

4. Ferrera L, Moran O (2006) β1-subunit modulates the NaV1.4 sodium channel by changing the surface charge. Exp Brain Res 172(2):139–150. https://doi.org/10.1007/s00221-005-0323-4

5. Goldin AL (2001) Resurgence of sodium channel research. Annu Rev Physiol 63(1):871–894. https://doi.org/10.1146/annurev.physiol.63.1.871

Cited by 1 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. The voltage-gated sodium channel inhibitor, 4,9-anhydrotetrodotoxin, blocks human Nav1.1 in addition to Nav1.6;Neuroscience Letters;2020-04

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