The effect of the adenosine A2A and A2B selective agonists, CGS 21680 and BAY 60-6583, on regional cardiovascular haemodynamics in conscious rats.

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Abstract

Background: and Purpose: Adenosine is a local mediator that regulates changes in the cardiovascular system via activation of four G protein-coupled receptors (A1, A2A, A2B, A3). Here we have investigated the effect of A2A and A2B-selective agonists on vasodilatation in three distinct vascular beds of the rat cardiovascular system. Experimental Approach: The regional haemodynamic effects of adenosine A2A and A2B selective agonists were investigated in conscious rats. Male Sprague-Dawley rats (350-450g) were chronically implanted with pulsed Doppler flow probes on the renal artery, mesenteric artery and the descending abdominal aorta. Cardiovascular responses were measured following intravenous infusion (3 min for each dose) of CGS 21680 (0.1, 0.3, 1 g.kg-1.min-1) or BAY 60-6583 (4,13.3, 40 g.kg-1.min-1) following pre-dosing with either SCH 58261 (0.1 or 1 mg.kg-1.min-1), PSB 1115 (10 mg.kg-1.min-1) or vehicle. Key Results: The A2A-selective agonist CGS 21680 produced a striking increase in heart rate (HR) and hindquarters vascular conductance (VC) that was accompanied by a significant decrease in mean arterial pressure (MAP) in conscious rats. In marked contrast, the A2B-selective agonist BAY 60-6583 significantly increased HR and VC in the renal and mesenteric vascular beds, but not in the hindquarters. Conclusions and Implications: Taken together, these data indicate that A2A and A2B receptors are regionally selective in their regulation of vascular tone. These results suggest that the development of A2B receptor agonists to induce vasodilatation in the kidney may provide a good therapeutic approach for the treatment of acute kidney injury.
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Abstract

Background and Purpose: Adenosine is a local mediator that regulates changes in the cardiovascular system via activation of four G protein-coupled receptors (A1, A2A, A2B, A3). Here we have investigated the effect of A2A and A2B-selective agonists on vasodilatation in three distinct vascular beds of the rat cardiovascular system. Experimental Approach: The regional haemodynamic effects of adenosine A2A and A2B selective agonists were investigated in conscious rats. Male Sprague-Dawley rats (350-450g) were chronically implanted with pulsed Doppler flow probes on the renal artery, mesenteric artery and the descending abdominal aorta. Cardiovascular responses were measured following intravenous infusion (3 min for each dose) of CGS 21680 (0.1, 0.3, 1 g.kg-1.min-1) or BAY 60-6583 (4,13.3, 40 g.kg-1.min-1) following pre-dosing with either SCH 58261 (0.1 or 1 mg.kg-1.min-1), PSB 1115 (10 mg.kg-1.min-1) or vehicle. Key Results: The A2A-selective agonist CGS 21680 produced a striking increase in heart rate (HR) and hindquarters vascular conductance (VC) that was accompanied by a significant decrease in mean arterial pressure (MAP) in conscious rats. In marked contrast, the A2B-selective agonist BAY 60-6583 significantly increased HR and VC in the renal and mesenteric vascular beds, but not in the hindquarters. Conclusions and Implications: Taken together, these data indicate that A2A and A2B receptors are regionally selective in their regulation of vascular tone. These results suggest that the development of A2B receptor agonists to induce vasodilatation in the kidney may provide a good therapeutic approach for the treatment of acute kidney injury. Supplementary Material File (bjp adenosine paper a2a a2b final v3.docx) - Download - 88.96 KB Information & Authors Information Version history Copyright This work is licensed under a Non Exclusive No Reuse License.

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Authors Metrics & Citations Metrics Article Usage 368views 144downloads Citations Download citation Samantha Cooper, Edward Wragg, Patrizia Pannucci, et al. The effect of the adenosine A2A and A2B selective agonists, CGS 21680 and BAY 60-6583, on regional cardiovascular haemodynamics in conscious rats.. Authorea. 31 January 2024. DOI: https://doi.org/10.22541/au.170669821.14280887/v1 DOI: https://doi.org/10.22541/au.170669821.14280887/v1 If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download. For more information or tips please see 'Downloading to a citation manager' in the Help menu.

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