Pharmacological characterization of Ca(2+) entry channels in endothelin-1-induced contraction of rat aorta using LOE 908 and SK&F 96365

1. We have recently shown that endothelin-1 (ET-1) activates two types of Ca(2+)-permeable nonselective cation channels (designated NSCC-1 and NSCC-2) and store-operated Ca(2+) channel (SOCC). These channels can be pharmacologically discriminated using Ca(2+) channel blockers such as SK&F 96365...

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Autori principali: Zhang, Xiao-Feng, Iwamuro, Yasushi, Enoki, Taijiro, Okazawa, Makoto, Lee, Ken, Komuro, Taro, Minowa, Tetsuya, Okamoto, Yasuo, Hasegawa, Hiroshi, Furutani, Hidekatsu, Miwa, Soichi, Masaki, Tomoh
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1999
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Papers
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1760648/
https://ncbi.nlm.nih.gov/pubmed/10455288
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjp.0702661
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