Thapsigargin Inhibits the Response to Acetylcholine and Substance P But Does Not Interfere with the Responses to Endothelium-Independent Agents-Reference-Cited by-同舟云学术

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Thapsigargin Inhibits the Response to Acetylcholine and Substance P But Does Not Interfere with the Responses to Endothelium-Independent Agents

Published:1996-07 Issue:1 Volume:28 Page:82-88
ISSN:0160-2446
Container-title:Journal of Cardiovascular Pharmacology
language:en
Short-container-title:Journal of Cardiovascular Pharmacology

Author:

Amerini Sandra,Filippi Sandra,Parenti Astrid,Ziche Marina,Ledda Fabrizio

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Pharmacology

Reference27 articles.

1. Thapsigargin, a tumor promoter, discharges intracellular Ca2+ stores by specific inhibition of the endoplasmic reticulum Ca2(+)-ATPase.

2. Regulation of extracellular calcium entry in endothelial cells: role of intracellular calcium pool

3. Thapsigargin, A Ca2+-ATPase inhibitor, relaxes rat aorta via nitric oxide formation

4. Thapsigargin induces an endothelium-dependent, intracellular calcium ion-dependent vasodilation in vitro

Cited by 11 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. Endothelium-dependent noradrenergic hyperresponsiveness induced by thapsigargin in human saphenous veins: role of thromboxane and calcium;European Journal of Pharmacology;2004-01

2. Mesaconitine-induced relaxation in rat aorta: role of Na+/Ca2+ exchangers in endothelial cells;European Journal of Pharmacology;2004-01

3. Ca2+-recruitment in tachykinin-induced contractions of gut smooth muscle from African clawed frog, Xenopus laevis and rainbow trout, Oncorhynchus mykiss;General and Comparative Endocrinology;2003-04

4. Altered Effect of Cyclopiazonic Acid on Endothelium-Dependent Relaxation in Femoral Arteries From Hypertensive Rats;Journal of Cardiovascular Pharmacology;2002-08

5. Mesaconitine-induced relaxation in rat aorta: involvement of Ca2+ influx and nitric-oxide synthase in the endothelium;European Journal of Pharmacology;2002-02

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