http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2013296441-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6330f21aec49aaddc02209b1920c4f49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_65fa13e9a9c7ffb0d683d9b587d0c4c0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-09
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filingDate 2012-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8ab2697ac102dd884fbf7243c0f8789
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee43310a89346db3cd9dacb26f9bfc60
publicationDate 2013-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2013296441-A1
titleOfInvention Anti-Obesity Properties of Pterostilbene
abstract We have determined that pterostilbene demonstrates anti-obesity properties. Rats were fed a commercial obesogenic diet supplemented or not with pterostilbene: PT15 (low dose: 15 mg/kg body weight/d) or PT30 (high dose: 30 mg/kg body weight/d) for 6 weeks. Pterostilbene significantly reduced total adipose tissue mass (15.1% in the PT15 group; 22.9% in the PT30 group) without changes in food intake. The activities of lipogenic enzymes were reduced in white adipose tissue and liver. Activities of enzymes involved in liver fatty acid oxidation were significantly increased in the PT30 group. Low dose pterostilbene can reduce body fat by reducing lipogenesis in adipose tissue. At the high dose, two mechanisms contribute to reduction in body fat: (1) decrease in adipose tissue and liver lipogenesis, and (2) an increase in liver fatty acid oxidation.
priorityDate 2012-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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