Abstract |
The vasodilatory effects of the synthetic rat atriopeptin (APII) have been studied in vitro in agonist-contracted, endothelium-denuded segments of the rat pulmonary artery, the ascending, and the distal abdominal aorta. In the pulmonary artery the contractures to methoxamine were inhibited more potently by APII (pD2 = 9.10 +/- 0.40, n = 6) than by the vasodilatory neuropeptide VIP (pD2 = 7.37 +/- 0.66, n = 6). The intrinsic activity of APII was 0.46 +/- 0.16 (n = 6). In segments previously exposed to either VIP or the beta 2-agonist salbutamol, APII was a near complete agonist (alpha = 0.82 +/- 0.17, n = 7 and 0.84 +/- 0.14, n = 6, respectively) without significant changes in the potencies. APII was a complete agonist also for the inhibition of the alpha-agonist-contracted segments of the aorta, however, with potencies 10-fold lower than in the pulmonary artery. VIP was without functionally significant effects in the aorta. The tachykinins (CGRP, SP, Neurokinins A and B) were without effects in all segments tested. In the ascending aorta, APII induced a long-lasting tachyphylaxis to the alpha-agonists, nearly completely abolishing the subsequent responsiveness to NA and methoxamine for more than 4 h.
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Authors | S Aardal, M Bråtveit, K B Helle |
Journal | Regulatory peptides
(Regul Pept)
Vol. 28
Issue 3
Pg. 283-92
(May 21 1990)
ISSN: 0167-0115 [Print] Netherlands |
PMID | 2377744
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Arrhythmia Agents
- Oligopeptides
- Tachykinins
- Vasoactive Intestinal Peptide
- antiarrhythmic peptide
- Methoxamine
- Albuterol
- Norepinephrine
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Topics |
- Albuterol
(pharmacology)
- Animals
- Anti-Arrhythmia Agents
(pharmacology)
- Aorta, Abdominal
(drug effects)
- Female
- In Vitro Techniques
- Methoxamine
(pharmacology)
- Norepinephrine
(pharmacology)
- Oligopeptides
(pharmacology)
- Pulmonary Artery
(drug effects)
- Rats
- Rats, Inbred Strains
- Tachykinins
(pharmacology)
- Vasoactive Intestinal Peptide
(pharmacology)
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