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Claire M Peppiattwildman - One of the best experts on this subject based on the ideXlab platform.
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supplementary material for an intact kidney slice model to investigate vasa recta properties and function in situ
2017Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E 2 ) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L -NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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an intact kidney slice model to investigate vasa recta properties and function in situ
Nephron Physiology, 2012Co-Authors: C Crawford, C Sprott, L Sawbridge, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E2) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L-NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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extracellular nucleotides affect Pericyte mediated regulation of rat in situ vasa recta diameter
Acta Physiologica, 2011Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, H Callaghan, Robert J Unwin, R L Simmons, Scott S P Wildman, Harriet M. Syme, Claire M PeppiattwildmanAbstract:AIM We hypothesized that extracellular nucleotides, established as being released from renal tubular epithelial cells, act at Pericytes to regulate vasa recta capillary diameter. METHODS A rat live kidney slice model and video imaging techniques were used to investigate the effects of extracellular nucleotides on in situ (subsurface) vasa recta diameter at Pericyte and non-Pericyte sites. In addition, RT-qPCR was used to quantify P2 receptor mRNA expression in isolated vasa recta. RESULTS Extracellular ATP, UTP, benzylbenzyl ATP (BzATP) or 2-methylthioATP (2meSATP) evoked a significantly greater vasoconstriction of subsurface vasa recta at Pericytes than at non-Pericyte sites. The rank order of agonist potency was BzATP = 2meSATP > ATP = UTP. The vasoconstriction evoked at Pericyte sites by ATP was significantly attenuated by the P2 receptor antagonists suramin, pyridoxal phosphate-6-azo(benzene-2,4-disulfonic acid) (PPADS) or Reactive Blue-2 (RB-2). UTP-evoked vasoconstriction at Pericytes was attenuated by suramin or RB-2 but not PPADS. Interestingly, suramin or PPADS, when applied in the absence of a P2 receptor agonist, evoked a weak but significant vasoconstriction of vasa recta at Pericyte sites, suggesting tonic vasodilation by nucleotides. Significant levels of P2X(1, 3 and 7) and P2Y(4 and 6) receptor mRNA were detected in vasa recta. CONCLUSION Extracellular nucleotides act at Pericytes to cause vasoconstriction of in situ vasa recta. Pharmacological characterization, supported by RT-qPCR data, suggests that P2X(1 and 7) and P2Y(4) receptors mediate nucleotide-evoked vasoconstriction of vasa recta by Pericytes. We propose that nucleotides released from renal tubular epithelial cells, in close proximity to vasa recta capillaries, are key in regulating renal medullary blood flow.
C Crawford - One of the best experts on this subject based on the ideXlab platform.
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supplementary material for an intact kidney slice model to investigate vasa recta properties and function in situ
2017Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E 2 ) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L -NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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an intact kidney slice model to investigate vasa recta properties and function in situ
Nephron Physiology, 2012Co-Authors: C Crawford, C Sprott, L Sawbridge, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E2) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L-NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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extracellular nucleotides affect Pericyte mediated regulation of rat in situ vasa recta diameter
Acta Physiologica, 2011Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, H Callaghan, Robert J Unwin, R L Simmons, Scott S P Wildman, Harriet M. Syme, Claire M PeppiattwildmanAbstract:AIM We hypothesized that extracellular nucleotides, established as being released from renal tubular epithelial cells, act at Pericytes to regulate vasa recta capillary diameter. METHODS A rat live kidney slice model and video imaging techniques were used to investigate the effects of extracellular nucleotides on in situ (subsurface) vasa recta diameter at Pericyte and non-Pericyte sites. In addition, RT-qPCR was used to quantify P2 receptor mRNA expression in isolated vasa recta. RESULTS Extracellular ATP, UTP, benzylbenzyl ATP (BzATP) or 2-methylthioATP (2meSATP) evoked a significantly greater vasoconstriction of subsurface vasa recta at Pericytes than at non-Pericyte sites. The rank order of agonist potency was BzATP = 2meSATP > ATP = UTP. The vasoconstriction evoked at Pericyte sites by ATP was significantly attenuated by the P2 receptor antagonists suramin, pyridoxal phosphate-6-azo(benzene-2,4-disulfonic acid) (PPADS) or Reactive Blue-2 (RB-2). UTP-evoked vasoconstriction at Pericytes was attenuated by suramin or RB-2 but not PPADS. Interestingly, suramin or PPADS, when applied in the absence of a P2 receptor agonist, evoked a weak but significant vasoconstriction of vasa recta at Pericyte sites, suggesting tonic vasodilation by nucleotides. Significant levels of P2X(1, 3 and 7) and P2Y(4 and 6) receptor mRNA were detected in vasa recta. CONCLUSION Extracellular nucleotides act at Pericytes to cause vasoconstriction of in situ vasa recta. Pharmacological characterization, supported by RT-qPCR data, suggests that P2X(1 and 7) and P2Y(4) receptors mediate nucleotide-evoked vasoconstriction of vasa recta by Pericytes. We propose that nucleotides released from renal tubular epithelial cells, in close proximity to vasa recta capillaries, are key in regulating renal medullary blood flow.
Scott S P Wildman - One of the best experts on this subject based on the ideXlab platform.
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supplementary material for an intact kidney slice model to investigate vasa recta properties and function in situ
2017Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E 2 ) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L -NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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an intact kidney slice model to investigate vasa recta properties and function in situ
Nephron Physiology, 2012Co-Authors: C Crawford, C Sprott, L Sawbridge, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E2) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L-NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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extracellular nucleotides affect Pericyte mediated regulation of rat in situ vasa recta diameter
Acta Physiologica, 2011Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, H Callaghan, Robert J Unwin, R L Simmons, Scott S P Wildman, Harriet M. Syme, Claire M PeppiattwildmanAbstract:AIM We hypothesized that extracellular nucleotides, established as being released from renal tubular epithelial cells, act at Pericytes to regulate vasa recta capillary diameter. METHODS A rat live kidney slice model and video imaging techniques were used to investigate the effects of extracellular nucleotides on in situ (subsurface) vasa recta diameter at Pericyte and non-Pericyte sites. In addition, RT-qPCR was used to quantify P2 receptor mRNA expression in isolated vasa recta. RESULTS Extracellular ATP, UTP, benzylbenzyl ATP (BzATP) or 2-methylthioATP (2meSATP) evoked a significantly greater vasoconstriction of subsurface vasa recta at Pericytes than at non-Pericyte sites. The rank order of agonist potency was BzATP = 2meSATP > ATP = UTP. The vasoconstriction evoked at Pericyte sites by ATP was significantly attenuated by the P2 receptor antagonists suramin, pyridoxal phosphate-6-azo(benzene-2,4-disulfonic acid) (PPADS) or Reactive Blue-2 (RB-2). UTP-evoked vasoconstriction at Pericytes was attenuated by suramin or RB-2 but not PPADS. Interestingly, suramin or PPADS, when applied in the absence of a P2 receptor agonist, evoked a weak but significant vasoconstriction of vasa recta at Pericyte sites, suggesting tonic vasodilation by nucleotides. Significant levels of P2X(1, 3 and 7) and P2Y(4 and 6) receptor mRNA were detected in vasa recta. CONCLUSION Extracellular nucleotides act at Pericytes to cause vasoconstriction of in situ vasa recta. Pharmacological characterization, supported by RT-qPCR data, suggests that P2X(1 and 7) and P2Y(4) receptors mediate nucleotide-evoked vasoconstriction of vasa recta by Pericytes. We propose that nucleotides released from renal tubular epithelial cells, in close proximity to vasa recta capillaries, are key in regulating renal medullary blood flow.
C Sprott - One of the best experts on this subject based on the ideXlab platform.
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supplementary material for an intact kidney slice model to investigate vasa recta properties and function in situ
2017Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E 2 ) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L -NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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an intact kidney slice model to investigate vasa recta properties and function in situ
Nephron Physiology, 2012Co-Authors: C Crawford, C Sprott, L Sawbridge, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E2) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L-NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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extracellular nucleotides affect Pericyte mediated regulation of rat in situ vasa recta diameter
Acta Physiologica, 2011Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, H Callaghan, Robert J Unwin, R L Simmons, Scott S P Wildman, Harriet M. Syme, Claire M PeppiattwildmanAbstract:AIM We hypothesized that extracellular nucleotides, established as being released from renal tubular epithelial cells, act at Pericytes to regulate vasa recta capillary diameter. METHODS A rat live kidney slice model and video imaging techniques were used to investigate the effects of extracellular nucleotides on in situ (subsurface) vasa recta diameter at Pericyte and non-Pericyte sites. In addition, RT-qPCR was used to quantify P2 receptor mRNA expression in isolated vasa recta. RESULTS Extracellular ATP, UTP, benzylbenzyl ATP (BzATP) or 2-methylthioATP (2meSATP) evoked a significantly greater vasoconstriction of subsurface vasa recta at Pericytes than at non-Pericyte sites. The rank order of agonist potency was BzATP = 2meSATP > ATP = UTP. The vasoconstriction evoked at Pericyte sites by ATP was significantly attenuated by the P2 receptor antagonists suramin, pyridoxal phosphate-6-azo(benzene-2,4-disulfonic acid) (PPADS) or Reactive Blue-2 (RB-2). UTP-evoked vasoconstriction at Pericytes was attenuated by suramin or RB-2 but not PPADS. Interestingly, suramin or PPADS, when applied in the absence of a P2 receptor agonist, evoked a weak but significant vasoconstriction of vasa recta at Pericyte sites, suggesting tonic vasodilation by nucleotides. Significant levels of P2X(1, 3 and 7) and P2Y(4 and 6) receptor mRNA were detected in vasa recta. CONCLUSION Extracellular nucleotides act at Pericytes to cause vasoconstriction of in situ vasa recta. Pharmacological characterization, supported by RT-qPCR data, suggests that P2X(1 and 7) and P2Y(4) receptors mediate nucleotide-evoked vasoconstriction of vasa recta by Pericytes. We propose that nucleotides released from renal tubular epithelial cells, in close proximity to vasa recta capillaries, are key in regulating renal medullary blood flow.
L Sawbridge - One of the best experts on this subject based on the ideXlab platform.
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supplementary material for an intact kidney slice model to investigate vasa recta properties and function in situ
2017Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E 2 ) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L -NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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an intact kidney slice model to investigate vasa recta properties and function in situ
Nephron Physiology, 2012Co-Authors: C Crawford, C Sprott, L Sawbridge, R J Unwin, Scott S P Wildman, Jgl Munday, Tejal A Desai, Claire M PeppiattwildmanAbstract:Background: Medullary blood flow is via vasa recta capillaries, which possess contractile Pericytes. In vitro studies using isolated descending vasa recta show that Pericytes can constrict/dilate descending vasa recta when vasoactive substances are present. We describe a live kidney slice model in which Pericyte-mediated vasa recta constriction/dilation can be visualized in situ. Methods: Confocal microscopy was used to image calcein, propidium iodide and Hoechst labelling in ‘live’ kidney slices, to determine tubular and vascular cell viability and morphology. DIC video-imaging of live kidney slices was employed to investigate Pericyte-mediated real-time changes in vasa recta diameter. Results: Pericytes were identified on vasa recta and their morphology and density were characterized in the medulla. Pericyte-mediated changes in vasa recta diameter (10–30%) were evoked in response to bath application of vasoactive agents (norepinephrine, endothelin-1, angiotensin-II and prostaglandin E2) or by manipulating endogenous vasoactive signalling pathways (using tyramine, L-NAME, a cyclo-oxygenase (COX-1) inhibitor indomethacin, and ATP release). Conclusions: The live kidney slice model is a valid complementary technique for investigating vasa recta function in situ and the role of Pericytes as regulators of vasa recta diameter. This technique may also be useful in exploring the role of tubulovascular crosstalk in regulation of medullary blood flow.
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extracellular nucleotides affect Pericyte mediated regulation of rat in situ vasa recta diameter
Acta Physiologica, 2011Co-Authors: C Crawford, C Sprott, L Sawbridge, T M Kennedylydon, H Callaghan, Robert J Unwin, R L Simmons, Scott S P Wildman, Harriet M. Syme, Claire M PeppiattwildmanAbstract:AIM We hypothesized that extracellular nucleotides, established as being released from renal tubular epithelial cells, act at Pericytes to regulate vasa recta capillary diameter. METHODS A rat live kidney slice model and video imaging techniques were used to investigate the effects of extracellular nucleotides on in situ (subsurface) vasa recta diameter at Pericyte and non-Pericyte sites. In addition, RT-qPCR was used to quantify P2 receptor mRNA expression in isolated vasa recta. RESULTS Extracellular ATP, UTP, benzylbenzyl ATP (BzATP) or 2-methylthioATP (2meSATP) evoked a significantly greater vasoconstriction of subsurface vasa recta at Pericytes than at non-Pericyte sites. The rank order of agonist potency was BzATP = 2meSATP > ATP = UTP. The vasoconstriction evoked at Pericyte sites by ATP was significantly attenuated by the P2 receptor antagonists suramin, pyridoxal phosphate-6-azo(benzene-2,4-disulfonic acid) (PPADS) or Reactive Blue-2 (RB-2). UTP-evoked vasoconstriction at Pericytes was attenuated by suramin or RB-2 but not PPADS. Interestingly, suramin or PPADS, when applied in the absence of a P2 receptor agonist, evoked a weak but significant vasoconstriction of vasa recta at Pericyte sites, suggesting tonic vasodilation by nucleotides. Significant levels of P2X(1, 3 and 7) and P2Y(4 and 6) receptor mRNA were detected in vasa recta. CONCLUSION Extracellular nucleotides act at Pericytes to cause vasoconstriction of in situ vasa recta. Pharmacological characterization, supported by RT-qPCR data, suggests that P2X(1 and 7) and P2Y(4) receptors mediate nucleotide-evoked vasoconstriction of vasa recta by Pericytes. We propose that nucleotides released from renal tubular epithelial cells, in close proximity to vasa recta capillaries, are key in regulating renal medullary blood flow.