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Angiotensin II Induces Leukocyte–Endothelial Cell Interactions In Vivo Via AT1 and AT2 Receptor–Mediated P-Selectin Upregulation

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Angiotensin II Induces Leukocyte–Endothelial Cell Interactions In Vivo Via AT1 and AT2 Receptor–Mediated P-Selectin Upregulation

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dc.contributor.author Piqueras Ruiz, Laura
dc.contributor.author Kubes, Paul
dc.contributor.author Álvarez Ribelles, Ángeles
dc.contributor.author O'Connor Blasco, José Enrique
dc.contributor.author Issekutz, Andrew C.
dc.contributor.author Esplugues Mota, Juan Vicente
dc.contributor.author Sanz Ferrando, María Jesús
dc.date.accessioned 2011-08-19T09:17:10Z
dc.date.available 2011-08-19T09:17:10Z
dc.date.issued 2000
dc.identifier.citation PIQUERAS RUIZ, Laura ; Kubes, Paul ; Alvarez Ribelles, Angeles ; O'Connor, Enrique ; Issekutz, Andrew C. ; Esplugues Mota, Juan Vicente ; Sanz Ferrando, Maria Jesus, 2000, Angiotensin II Induces Leukocyte–Endothelial Cell Interactions In Vivo Via AT1 and AT2 Receptor–Mediated P-Selectin Upregulation, Circulation, vol. 102, no. 17, p. 2118-2123 en
dc.identifier.uri http://hdl.handle.net/10550/20058
dc.description.abstract Background—Angiotensin II (Ang II) plays a critical role in the development of vascular lesions in hypertension, atherosclerosis, and several renal diseases. Because Ang II may contribute to the leukocyte recruitment associated with these pathological states, the aim of the present study was to assess the role of Ang II in leukocyte–endothelial cell interactions in vivo. Methods and Results—Intravital microscopy of the rat mesenteric postcapillary venules was used. Sixty minutes of superfusion with 1 nmol/L Ang II induced a significant increase in leukocyte rolling flux (83.8±20.7 versus 16.4±3.1 cells/min), adhesion (11.4±1.0 versus 0.8±0.5 cells/100 µm), and emigration (4.0±0.7 versus 0.2±0.2 cells/field) without any vasoconstrictor activity. These effects were not mediated by mast cell activation. Intravenous pretreatment with AT1 (losartan) or AT2 (PD123,319) receptor antagonists significantly reduced Ang II–induced responses. A combination of both receptor antagonists inhibited the leukocyte rolling flux, adhesion, and extravasation elicited by Ang II at 60 minutes. Pretreatment of animals with fucoidin or an adhesion-blocking anti–rat P-selectin monoclonal antibody abolished Ang II–induced leukocyte responses. Furthermore, rat platelet P-selectin expression was not affected by Ang II stimulation. Conclusions—Ang II induces significant leukocyte rolling, adhesion, and emigration, which may contribute not only to hypertension but also to the onset and progression of the vascular damage associated with disease states in which plasma levels of this peptide are elevated. en
dc.language.iso en en
dc.subject Angiotensin ; Endothelium ; Leukocytes ; Cell adhesion molecules ; Glycoproteins en
dc.title Angiotensin II Induces Leukocyte–Endothelial Cell Interactions In Vivo Via AT1 and AT2 Receptor–Mediated P-Selectin Upregulation en
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS en
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS ::Medicina interna en
dc.identifier.idgrec 003711 en
dc.type.hasVersion VoR es_ES
dc.identifier.url http://circ.ahajournals.org/cgi/reprint/102/17/2118 en

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