ET <sub>A</sub> Receptor Mediates Altered Leukocyte-Endothelial Cell Interaction and Adhesion Molecules Expression in DOCA–Salt Rats

DOI Web Site 被引用文献3件
  • Glaucia E. Callera
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Augusto C. Montezano
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Rhian M. Touyz
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Telma M.T. Zorn
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Maria Helena C. Carvalho
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Zuleica B. Fortes
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Dorothy Nigro
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Ernesto L. Schiffrin
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.
  • Rita C. Tostes
    From the Departments of Pharmacology (G.E.C., A.C.M., M.H.C.C., Z.B.F., D.N., R.C.T.) and Histology and Embryology (T.M.T.Z.), Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil; and Clinical Research Institute of Montreal (G.E.C., R.M.T., E.L.S.), University of Montreal, Montreal, Canada.

抄録

<jats:p> Leukocyte adhesion to endothelial cells plays a key role in inflammatory processes associated with end-organ injury. Endothelin-1 (ET-1), which stimulates inflammatory processes, contributes to cardiovascular damage in deoxycorticosterone (DOCA)–salt hypertension. We investigated whether ET <jats:sub>A</jats:sub> receptor blockade modulates in vivo leukocyte–endothelial cell interactions and expression of cell adhesion molecules (CAM) involved in these processes. DOCA–salt and control uninephrectomized rats were treated with the ET <jats:sub>A</jats:sub> antagonist BMS182874 (40 mg/kg per day) or vehicle. Analysis of CAMs expression by reverse transcription-polymerase chain reaction and immunohistochemistry showed increased cardiac platelet selectin (P-selectin), detected mainly in endothelial cells, and vascular cell adhesion molecule-1 (VCAM-1), but not intercellular adhesion molecule-1 (ICAM-1), in DOCA–salt rats. Cardiac expression of endothelial selectin (E-selectin) was decreased, whereas immunoreactivity to ED-1 and myeloperoxidase (MPO) activity, markers of macrophage and leukocyte infiltration, respectively, were increased in DOCA-salt. Leukocyte–endothelial cell interaction, functionally assessed in venules of internal spermatic fascia by intravital microscopy, was significantly altered in DOCA–salt rats as evidenced by increased leukocyte adhesion and decreased rolling. BMS182874 treatment normalized leukocyte–endothelium interactions, decreased cardiac VCAM-1 expression in DOCA and control groups, and had no effects on ICAM-1 expression. BMS182874 also increased E-selectin and abolished P-selectin expression in DOCA-salt, but not in control rats. The ET <jats:sub>A</jats:sub> antagonist reduced cardiac ED-1 content and MPO activity and prevented cardiac damage in DOCA–salt rats. These data indicate that ET-1 participates, via activation of ET <jats:sub>A</jats:sub> receptors, in altered leukocyte–endothelial cell interactions in DOCA–salt rats, possibly by modulating expression of CAMs, and that the inflammatory status is associated with cardiac damage in mineralocorticoid hypertension. </jats:p>

収録刊行物

  • Hypertension

    Hypertension 43 (4), 872-879, 2004-04

    Ovid Technologies (Wolters Kluwer Health)

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