Are Multiple Angiotensin Receptor Types Involved in Angiotensin (1-7) Actions on Isolated Rat Portal Vein?
Author(s) -
Bogdan Gurzu,
Marcel Costuleanu,
Simona Mihaela Slătineanu,
Aurica Ciobanu,
G Petrescu
Publication year - 2005
Publication title -
journal of the renin-angiotensin-aldosterone system
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 46
eISSN - 1752-8976
pISSN - 1470-3203
DOI - 10.3317/jraas.2005.015
Subject(s) - angiotensin ii , losartan , receptor , renin–angiotensin system , portal vein , endocrinology , medicine , chemistry , angiotensin iii , angiotensin receptor , angiotensin ii receptor type 1 , biology , blood pressure
Angiotensin (1-7) [Ang (1-7)] is a bioactive component of the renin angiotensin system. Ang (1-7) may interact with angiotensin type 1 (AT 1 ) or type 2 (AT 2 ) receptors and with Ang (1-7) — specific receptors. We examined the interactions between different doses of Ang (1-7) (1nM-1microM) and angiotensin II (Ang II) (10 and 100nM) on isolated rat portal vein. In endothelium-denuded portal vein rings, Ang (1-7) inhibited contractile effects induced by Ang II. The effects of Ang (1-7) were modified by indomethacin, N(G)-nitro-L-arginine methyl ester (L-NAME), (D-Ala 7 )-Angiotensin (1-7) (H-2888) and losartan. Our results suggest that on rat isolated portal vein rings without endothelium, Ang (1-7) reduces Ang II—induced contractions by acting mostly on Ang (1-7) specific receptors, and this effect is mediated by vasodilatatory prostaglandins. At high concentrations, Ang (1-7) effects are mediated by AT 1 -receptors, though to a lesser extent than by Ang (1-7) specific receptors.
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