<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>Altirriba, Jordi</dc:creator>
  <dc:creator>Poher, Anne-Laure</dc:creator>
  <dc:creator>Caillon, Aurélie</dc:creator>
  <dc:creator>Arsenijevic, Denis</dc:creator>
  <dc:creator>Veyrat-Durebex, Christelle</dc:creator>
  <dc:creator>Lyautey, Jacqueline</dc:creator>
  <dc:creator>Dulloo, Abdul G.</dc:creator>
  <dc:creator>Rohner-Jeanrenaud, Françoise</dc:creator>
  <dc:date>2014-08-26</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Oxytocin has been suggested as a novel therapeutic against obesity, because it  induces weight loss and improves glucose tolerance in diet-induced obese rodents. A  recent clinical pilot study confirmed the oxytocin-induced weight-reducing effect in  obese nondiabetic subjects. Nevertheless, the mechanisms involved and the impact  on the main comorbidity associated with obesity, type 2 diabetes, are unknown. Lean  and ob/ob mice (model of obesity, hyperinsulinemia, and diabetes) were treated for 2  weeks with different doses of oxytocin, analogues with longer half-life (carbetocin) or  higher oxytocin receptor specificity ([Thr4,Gly7]-oxytocin). Food and water intake,  body weight, and glycemia were measured daily. Glucose, insulin, and pyruvate  tolerance, body composition, several hormones, metabolites, gene expression, as well  as enzyme activities were determined. Although no effect of oxytocin on the main  parameters was observed in lean mice, the treatment dose-dependently reduced food  intake and body weight gain in ob/ob animals. Carbetocin behaved similarly to  oxytocin, whereas [Thr4,Gly7]-oxytocin (TGOT) and a low oxytocin dose decreased  body weight gain without affecting food intake. The body weight gain-reducing effect  was limited to the fat mass only, with decreased lipid uptake, lipogenesis, and  inflammation, combined with increased futile cycling in abdominal adipose tissue.  Surprisingly, oxytocin treatment of ob/ob mice was accompanied by a worsening of  basal glycemia and glucose tolerance, likely due to increased corticosterone levels  and stimulation of hepatic gluconeogenesis. These results impose careful selection of  the conditions in which oxytocin treatment should be beneficial for obesity and its  comorbidities, and their relevance for human pathology needs to be determined.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/303937</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/303937/files/dul_deo.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/303937/files/dul_deo_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1210/en.2014-1466</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Endocrinology. - 2014, vol. 155, no. 11, p. 4189–4201</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Divergent effects of oxytocin treatment of obese diabetic mice on adiposity and diabetes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
