Rozh H. Al-Mashhadi, Ole Skøtt, Paul M. Vanhoutte, Pernille B. Hansen 

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Activation of A2 adenosine receptors dilates cortical efferent arterioles in mouse  Rozh H. Al-Mashhadi, Ole Skøtt, Paul M. Vanhoutte, Pernille B. Hansen  Kidney International  Volume 75, Issue 8, Pages 793-799 (April 2009) DOI: 10.1038/ki.2008.684 Copyright © 2009 International Society of Nephrology Terms and Conditions

Figure 1 Concentration–response relationship for adenosine (ado) and CHA in mouse superficial efferent arterioles. (a) Adenosine was administered to the bath solution every third minute in cumulatively increasing concentrations. Data are means±s.e.m. (n=5). (b) Increasing concentrations of CHA applied to the bath solution. Data are means±s.e.m. (n=5). Kidney International 2009 75, 793-799DOI: (10.1038/ki.2008.684) Copyright © 2009 International Society of Nephrology Terms and Conditions

Figure 2 Effect of the thromboxane receptor agonist U46619 in mouse superficial efferent arterioles. (a) Cumulatively increasing concentrations of U46619 were added to the bath every third minute. Full constriction was seen with 10-7 mol/l. Basal diameter (Basal) before U46619 administration is set to 100%. Data are means±s.e.m. (n=5). (b) Application of 10-7 mol/l U46619 for 21 min. Each arrow represents bath substitution with new medium containing 10-7 mol/l U46619. Data are means±s.e.m. (n=3). (c) Photograph of an isolated perfused mouse efferent arteriole under basal conditions. (d) Efferent arteriole constricted with U46619 (10-7 mol/l). Kidney International 2009 75, 793-799DOI: (10.1038/ki.2008.684) Copyright © 2009 International Society of Nephrology Terms and Conditions

Figure 3 Reproducible concentration–dilatation curves to adenosine (ado) and NECA in arterioles constricted with U46619. ‘Basal’ represents basal vessel diameters before application of adenosine or NECA. (a) Adenosine was added to the bath solution every third minute in cumulatively increasing concentrations. Data are means±s.e.m. (n=4; *P<0.05 vs U46619). (b) Increasing concentrations of NECA applied to the bath every third minute. Data are means±s.e.m. (n=5). Kidney International 2009 75, 793-799DOI: (10.1038/ki.2008.684) Copyright © 2009 International Society of Nephrology Terms and Conditions

Figure 4 Concentration–response relationship for adenosine (ado) in arterioles constricted with U46619 in the absence (left) and presence (right) of DMPX. Data are means±s.e.m. (n=5; *P<0.001 vs U46619). Kidney International 2009 75, 793-799DOI: (10.1038/ki.2008.684) Copyright © 2009 International Society of Nephrology Terms and Conditions

Figure 5 Effect of adenosine (ado) in the presence of the A2AR antagonist DMPX. The plot shows diameter of the same blood vessel during adenosine application before and after treatment with DMPX. Diameters for each application are expressed as percent of vessel diameter before treatment. Data are means±s.e.m. (n=8; P>0.05 for ado vs DMPX+ado). Kidney International 2009 75, 793-799DOI: (10.1038/ki.2008.684) Copyright © 2009 International Society of Nephrology Terms and Conditions

Figure 6 Expression of adenosine receptors in mouse superficial arterioles. Bands of the expected size were obtained for A1AR, A2aAR, A2bAR, and A3AR in efferent arterioles (Eff. art., a), afferent arterioles (Aff. art., b), and in the positive control using whole kidney. The negative control, water, expressed no bands. Kidney International 2009 75, 793-799DOI: (10.1038/ki.2008.684) Copyright © 2009 International Society of Nephrology Terms and Conditions