<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Barton M</dc:creator>
  <dc:creator>Shaw S</dc:creator>
  <dc:creator>d'Uscio LV</dc:creator>
  <dc:creator>Moreau P</dc:creator>
  <dc:creator>Lüscher TF</dc:creator>
  <dc:date>1997</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Angiotensin II (Ang II)-stimulated expression of endothelin-1 (ET-1) mRNA is blocked by ETA antagonists in vitro. We studied effects of Ang II (200 ng/kg/min) and ETA antagonist LU135252 (50 mg/kg/d) in WKY rats in vivo investigating vascular and renal ET-1 protein expression, functional endothelin converting enzyme (ECE) activity, and clearance of (125I)ET-1. Infusion of Ang II for two weeks increased ET-1 protein content in aorta (4.7-fold) and femoral artery (1.6-fold) with and without endothelium and in kidneys (3-fold, p&lt;0.05) and enhanced functional ECE activity (p&lt;0.05). The Ang II-induced increase in tissue ET-1 content and functional ECE activity was completely prevented by LU135252 (p&lt;0.05). Chronic treatment of control animals with LU135252 lowered basal vascular but not renal ET-1 content (p&lt;0.05 vs. control). Clearance of 125IET-1 was unaffected by the treatments. It is concluded that Ang II increases ET-1 protein and functional ECE activity in vascular smooth muscle and kidney through ETA-receptors in vivo.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/185654</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1006/bbrc.1997.7394</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/9325182</dc:relation>
  <dc:source>Biochemical and biophysical research communications. - 1997</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Angiotensin II</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Aorta</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Aspartic Acid Endopeptidases</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Blood Pressure</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Endothelin Receptor Antagonists</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Endothelin-1</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Endothelin-Converting Enzymes</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Femoral Artery</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">In Vitro Techniques</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Iodine Radioisotopes</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Kidney</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Metalloendopeptidases</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Muscle Contraction</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Phenylpropionates</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Pyrimidines</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Rats</dc:subject>
  <dc:subject xmlns:ns19="xml" ns19:lang="en">Rats, Inbred WKY</dc:subject>
  <dc:subject xmlns:ns20="xml" ns20:lang="en">Receptor, Endothelin A</dc:subject>
  <dc:subject xmlns:ns21="xml" ns21:lang="en">Receptors, Endothelin</dc:subject>
  <dc:title xmlns:ns22="xml" ns22:lang="en">Angiotensin II increases vascular and renal endothelin-1 and functional endothelin converting enzyme activity in vivo: role of ETA receptors for endothelin regulation.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
