<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>Schneiter P</dc:creator>
  <dc:creator>Gillet M</dc:creator>
  <dc:creator>Chioléro R</dc:creator>
  <dc:creator>Jéquier E</dc:creator>
  <dc:creator>Tappy L</dc:creator>
  <dc:date>1999</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Seven patients with liver cirrhosis and five healthy subjects were studied over 4 hours after ingestion of a glucose meal to determine whether alterations of hepatic nonoxidative glucose disposal participate in the pathogenesis of impaired glucose tolerance. Hepatic uridyl-diphosphoglucose (UDPG) turnover was calculated from the isotopic enrichment of urinary acetaminophen glucuronide during continuous infusion of 13C-galactose and used as an index of hepatic glycogen synthesis. Patients with cirrhosis had postprandial hyperglycemia and decreased glucose clearance, but hepatic UDPG turnover was not altered (1.84 +/- 0.29 mg/kg fat-free mass min v 1.76 +/- 0.15 in controls, nonsignificant). It is concluded that hepatic postprandial glycogen synthesis is unaltered in patients with advanced cirrhosis, demonstrating important hepatic functional reserve.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/277803</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/s0026-0495(99)90265-2</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/10535388</dc:relation>
  <dc:source>Metabolism: clinical and experimental. - 1999</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Adult</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Carbon Isotopes</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Eating</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Female</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Galactose</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Glucose</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Glucose Intolerance</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Hyperglycemia</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Intestinal Absorption</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Liver</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Liver Cirrhosis</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Liver Glycogen</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Middle Aged</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Postprandial Period</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Prothrombin Time</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Reference Values</dc:subject>
  <dc:subject xmlns:ns19="xml" ns19:lang="en">Uridine Diphosphate Glucose</dc:subject>
  <dc:title xmlns:ns20="xml" ns20:lang="en">Hepatic nonoxidative disposal of an oral glucose meal in patients with liver cirrhosis.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
