Pharmacological characterization of Ca2+entry channels in endothelin-1-induced contraction of rat aorta using LOE 908 and SK&F 96365-Reference-Cited by-同舟云学术

Pharmacological characterization of Ca2+entry channels in endothelin-1-induced contraction of rat aorta using LOE 908 and SK&F 96365

Published:1999-07 Issue:6 Volume:127 Page:1388-1398
ISSN:0007-1188
Container-title:British Journal of Pharmacology
language:en
Short-container-title:

Author:

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

Publisher

Wiley

Subject

Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1038/sj.bjp.0702661/fullpdf

Reference35 articles.

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3. Endothelin induces a nonselective cation current in vascular smooth muscle cells;CHEN;Circ. Res.,1991

4. Pharmacology of endothelin-1 in isolated vessels: effect of nifedipine, methylene blue, hemoglobin, and gossypol;D'ORLEANS-JUSTE;J. Cardiovasc. Pharmacol.,1989

5. Inhibition of a store-operated Ca2+ entry pathway in human endothelial cells by the isoquinoline derivative LOE 908;ENCABO;Br. J. Pharmacol.,1996

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