✦ LIBER ✦

Overlap in the Pharmacology of L-type Ca2+ -channel Blockers and 5-HT2 Receptor Antagonists in Rat Aorta*

✍ Scribed by E. O. Okoro

Book ID: 111769841
Publisher: Pharmaceutical Press
Year: 1999
Tongue: English
Weight: 70 KB
Volume: 51
Category: Article
ISSN: 2042-7158
DOI: 10.1211/0022357991773221

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Ca2+ channel and 5-HT2 receptor anta

The Ca2+ channel and 5-HT2 receptor antagonist (s)-emopamil in cerebral ischaemia

✍ F.V. Defeudis 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 409 KB

Pharmacological characteristics of recep

Pharmacological characteristics of receptor-operated and potential-operated Ca2+ channels in rat aorta

✍ Andrew T. Chiu; Dale E. McCall; Pieter B.M.W.M. Timmermans 📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 619 KB

2.507 Effect of L-type Ca2 channel antag

2.507 Effect of L-type Ca2 channel antagonist, Isradipine, in the rat model of dyskinesia

✍ S. Schuster; E. Doudnikoff; C. Ittrich; B. Bloch; B. Hengerer; E. Bezard 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 53 KB

Effects of Ca2+antagonists and K+-channe

Effects of Ca2+antagonists and K+-channel activators on K+-induced contractions in the rat aorta

✍ Lawson, K. ;Cavero, I. 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 555 KB

Antisympathetic and hemodynamic property

Antisympathetic and hemodynamic property of a dual L/N-type Ca2+ channel blocker cilnidipine in rats

✍ Akira Takahara; Hajime Koganei; Tomoko Takeda; Seinosuke Iwata 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 188 KB

Mechanism of down-regulation of L-type C

Mechanism of down-regulation of L-type Ca2+ channel in the proliferating smooth muscle cells of rat aorta

✍ Eikichi Ihara; Katsuya Hirano; Mayumi Hirano; Junji Nishimura; Hajime Nawata; Hi 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 223 KB

The mechanism of down-regulation of L-type Ca(2+) channel (L-VOC) was investigated in rat aortic smooth muscle cells in primary culture. On culture days 3-5, the cells actively incorporated the 5-bromo-2'-deoxy-uridine (BrdU), and did not respond to K(+) depolarization nor express alpha(1C) subunit