Angiotensin II Type 2 Receptor Vasoactivity in Internal Mammary Arteries of Patients With Coronary Artery Disease

Autor: R. M. A van de Wal, H.W.M. Plokker, Georg Nickenig, W. J. Morshuis, D. J. Van Veldhuisen, W. H. Van Gilst, P. van der Harst, Hendrik Buikema, Lodewijk J. Wagenaar, Sven Wassmann, A. A. Voors
Rok vydání: 2007
Předmět:
Male
Angiotensin receptor
Pyridines
Vasodilator Agents
Gene Expression
Tetrazoles
Vasodilation
Coronary Artery Disease
Phenylephrine
Vasoconstrictor Agents
Receptor
Mesenteric arteries
Aged
80 and over

Angiotensin II
Imidazoles
Middle Aged
Receptor antagonist
medicine.anatomical_structure
cardiovascular system
Female
Cardiology and Cardiovascular Medicine
Oligopeptides
hormones
hormone substitutes
and hormone antagonists

medicine.drug
Adult
medicine.medical_specialty
medicine.drug_class
In Vitro Techniques
Receptor
Angiotensin
Type 2

Receptor
Angiotensin
Type 1

Internal medicine
medicine
Humans
Mammary Arteries
Phentolamine
Adrenergic alpha-Antagonists
Aged
Pharmacology
Angiotensin II receptor type 1
Sodium Nitrite
business.industry
Biphenyl Compounds
Acetylcholine
Candesartan
Endocrinology
Benzimidazoles
business
Angiotensin II Type 1 Receptor Blockers
Zdroj: Journal of Cardiovascular Pharmacology. 50:372-379
ISSN: 0160-2446
Popis: Background: Several animal studies suggested that the angiotensin II type 2 (AT2) receptor subtype mediates vasodilation, yet the results in human arteries are less well described and more inconsistent. Therefore, we evaluated the role of the AT2 receptor stimulation on the vasotonus of human internal mammary arteries. Methods: Internal mammary arteries were obtained from 50 patients undergoing coronary bypass surgery. The expression of angiotensin II type I (AT1) receptor and AT2 receptor mRNA was determined by using real-time polymerase chain reaction. In addition, angiotensin II and CGP42112A concentration-response curves (concentration range: 10(-10) M to 10(-6) M) were constructed in absence or presence of candesartan (10(-5) M) and/or the AT2 receptor-antagonist PD-123319 (10-6 M) and/or the a receptor antagonist phentolamine. Results: Both AT1 and AT2 receptor protein and mRNA were detected, and higher AT2 receptor mRNA expression levels were associated with increased contractile response to angiotensin II. Angiotensin II caused vasoconstriction up to 41.1 +/- 6.5% of the maximal response to phenylephrine, and PD123319 significantly reduced this response (28.6 +/- 9.6%, P
Databáze: OpenAIRE