Effects of Bepridil and Pimozide, Existing Medicines Capable of Blocking T-Type Ca2+ Channels, on Visceral Pain in Mice
Author:
Affiliation:
1. Laboratory of Pharmacology and Pathophysiology, Faculty of Pharmacy, Kindai University
Publisher
Pharmaceutical Society of Japan
Subject
Pharmaceutical Science,Pharmacology,General Medicine
Link
https://www.jstage.jst.go.jp/article/bpb/44/3/44_b20-00742/_pdf
Reference23 articles.
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2. 2) Weiss N, Zamponi GW. T-type calcium channels: from molecule to therapeutic opportunities. Int. J. Biochem. Cell Biol., 108, 34–39 (2019).
3. 3) Snutch TP, Zamponi GW. Recent advances in the development of T-type calcium channel blockers for pain intervention. Br. J. Pharmacol., 175, 2375–2383 (2018).
4. 4) Uchino T, Lee TS, Kaku T, Yamashita N, Noguchi T, Ono K. Voltage-dependent and frequency-independent inhibition of recombinant Cav3.2 T-type Ca2+ channel by bepridil. Pharmacology, 74, 174–181 (2005).
5. 5) Santi CM, Cayabyab FS, Sutton KG, McRory JE, Mezeyova J, Hamming KS, Parker D, Stea A, Snutch TP. Differential inhibition of T-type calcium channels by neuroleptics. J. Neurosci., 22, 396–403 (2002).
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