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Taraxerone enhances alcohol oxidation via increases of alcohol dehyderogenase (ADH) and acetaldehyde dehydrogenase (ALDH) activities and gene expressions.

Abstract
The present study, taraxerone (d-friedoolean-14-en-3-one) was isolated from Sedum sarmentosum with purity 96.383%, and its enhancing effects on alcohol dehydrogenase (ADH) and acetaldehyde dehydrogenase (ALDH) activities were determined: EC(50) values were 512.42 ± 3.12 and 500.16 ± 3.23 μM for ADH and ALDH, respectively. In order to obtain more information on taraxerone related with the alcohol metabolism, 40% ethanol (5 mL/kg body weight) with 0.5-1mM of taraxerone were administered to mice. The plasma alcohol and acetaldehyde concentrations of taraxerone-treated groups were significantly lowered than those of the control group (p<0.01): approximately 20-67% and 7-57% lowered for plasma alcohol and acetaldehyde, respectively. Compare to the control group, the ADH and ALDH expressions in the liver tissues were abruptly increased in the taraxerone-treated groups after ethanol exposure. In addition, taraxerone prevented catalase, superoxide dismutase, and reduced glutathione concentrations from the decrease induced by ethanol administration with the concentration dependent manner.
AuthorsChang-Keun Sung, Seung-Mi Kim, Chang-Jin Oh, Sun-A Yang, Byung-Hee Han, Eun-Kyoung Mo
JournalFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association (Food Chem Toxicol) Vol. 50 Issue 7 Pg. 2508-14 (Jul 2012) ISSN: 1873-6351 [Electronic] England
PMID22554647 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Ltd. All rights reserved.
Chemical References
  • Alcohols
  • DNA Primers
  • Oleanolic Acid
  • Alcohol Dehydrogenase
  • Aldehyde Oxidoreductases
  • aldehyde dehydrogenase (NAD(P)+)
  • taraxerone
Topics
  • Alcohol Dehydrogenase (metabolism)
  • Alcohols (metabolism)
  • Aldehyde Oxidoreductases (metabolism)
  • Animals
  • Base Sequence
  • DNA Primers
  • Gene Expression Regulation, Enzymologic
  • Mice
  • Oleanolic Acid (analogs & derivatives, pharmacology)
  • Oxidation-Reduction
  • Reverse Transcriptase Polymerase Chain Reaction

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