Ca2+ Entry Channels Involved in Contractions of Rat Aorta Induced by Endothelin-1, Noradrenaline, and Vasopressin-Reference-Cited by-同舟云学术

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Ca2+ Entry Channels Involved in Contractions of Rat Aorta Induced by Endothelin-1, Noradrenaline, and Vasopressin

Published:2002-08 Issue:2 Volume:40 Page:265-276
ISSN:0160-2446
Container-title:Journal of Cardiovascular Pharmacology
language:en
Short-container-title:Journal of Cardiovascular Pharmacology

Author:

Furutani Hidekatsu,Zhang Xiao-Feng,Iwamuro Yasushi,Lee Ken,Okamoto Yasuo,Takikawa Osamu,Fukao Mitsuhiro,Masaki Tomoh,Miwa Soichi

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Pharmacology

Reference36 articles.

1. A novel potent vasoconstrictor peptide produced by vascular endothelial cells

2. Physiological Role of Ca2+-Permeable Nonselective Cation Channel in Endothelin-1-Induced Contraction of Rabbit Aorta

3. Role of nonselective cation channels as Ca2+ entry pathway in endothelin-1-induced contraction and their suppression by nitric oxide

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

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