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Adenosine elicits an eNOS‐independent reduction in arterial blood pressure in conscious mice that involves adenosine A 2A receptors
Author(s) -
Andersen H.,
Jaff M. G.,
Høgh D.,
Vanhoutte P.,
Hansen P. B.
Publication year - 2011
Publication title -
acta physiologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.591
H-Index - 116
eISSN - 1748-1716
pISSN - 1748-1708
DOI - 10.1111/j.1748-1716.2010.02218.x
Subject(s) - adenosine , cgs 21680 , medicine , adenosine receptor , endocrinology , adenosine a1 receptor , enos , adenosine a2a receptor , mean arterial pressure , receptor , myograph , adenosine a3 receptor , blood pressure , chemistry , nitric oxide synthase , nitric oxide , heart rate , agonist
Abstract Aims: Adenosine plays an important role in the regulation of heart rate (HR) and vascular reactivity. However, the mechanisms underlying the acute effect of adenosine on arterial blood pressure in conscious mice are unclear. Therefore, this study investigated the effect of the nucleoside on mean arterial blood pressure (MAP) and HR in conscious mice. Methods: Chronic indwelling catheters were placed in C57Bl/6J (WT) and endothelial nitric oxide synthase knockout (eNOS −/− ) mice for continuous measurements of MAP and HR. Using PCR and myograph analysis, involvement of adenosine receptors was investigated in human and mouse renal blood vessels. Results: Bolus infusion of 0.5 mg kg −1 adenosine elicited significant transient decreases in MAP (99.3 ± 2.3 to 70.4 ± 4.5 mmHg) and HR (603.2 ± 18.3 to 364.3 ± 49.2 min −1 ), which were inhibited by the A 2A receptor antagonist ZM 241385. Activation of adenosine A 2A receptors with CGS 21680 (0.02 mg kg −1 ) caused a significant reduction in MAP from 99.6 ± 1.2 to 73.1 ± 3.6 mmHg accompanied by tachycardia (610.5 ± 9.3 to 677.5 ± 9.5 min −1 ). The reduction in MAP observed after adenosine or CGS 21680 administrations was not significantly different in WT and eNOS −/− mice. In isolated human and mouse intrarenal arteries, adenosine caused a relaxation dependent on A 2A adenosine receptor activation. A 2A receptors were present in both human and mouse arteries whereas A 1 and A 2B receptors were only present in mouse arteries. Conclusion: In conclusion, acute adenosine administration and selective stimulation of adenosine A 2A receptors results in an immediate, transient eNOS‐independent reduction in MAP. A 2A receptor activation causes relaxation of human and mouse arteries.