<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>Del Prete E</dc:creator>
  <dc:creator>Lutz TA</dc:creator>
  <dc:creator>Althaus J</dc:creator>
  <dc:creator>Scharrer E</dc:creator>
  <dc:date>1998</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Several lines of evidence indicate that fatty acid oxidation contributes to control of eating. We examined the effect of inhibitors of fatty acid oxidation (mercaptoacetate, R-3-amino-4-trimethylaminobutyric acid = emeriamine) on food intake in mice because fatty acid oxidation has been shown recently to increase the hepatic membrane potential in mouse liver, and this potential has been proposed to represent a signal for control of food intake. The effect of intraperitoneal injection of mercaptoacetate (200, 400, or 600 micromol/kg body weight) and emeriamine dihydrochloride (8.7, 17.4, 34.8, or 69.6 micromol/kg body weight) was investigated in mice fed a fat-enriched diet (18% fat). Both mercaptoacetate (400 or 600 micromol/kg) and emeriamine (34.8 or 69.6 micromol/kg) significantly increased food intake. These results suggest that fatty acid oxidation is also involved in feeding control in mice. Therefore, the pertinent mechanisms can be studied in mice.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/185684</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/s0031-9384(97)00527-1</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/9617995</dc:relation>
  <dc:source>Physiology &amp; behavior. - 1998</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Betaine</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Carnitine</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Dietary Fats</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Dose-Response Relationship, Drug</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Eating</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Enzyme Inhibitors</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Fatty Acids</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Hypoglycemic Agents</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Injections, Intraperitoneal</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Mice, Inbred ICR</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Oxidation-Reduction</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Thioglycolates</dc:subject>
  <dc:title xmlns:ns16="xml" ns16:lang="en">Inhibitors of fatty acid oxidation (mercaptoacetate, R-3-amino-4-trimethylaminobutyric acid) stimulate feeding in mice.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
