Plant-Derived Monoterpenes Suppress Hamster Kidney Cell 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Synthesis at the Post-Transcriptional Level
Author:
Affiliation:
1. Dennis M. Peffley, University of Health Sciences, Department of Biochemistry, Kansas City, MO 64106-1453
2. Apurba Gayen, Finch University of Health Sciences/The Chicago Medical School, North Chicago, IL 60064-3095
Publisher
Oxford University Press (OUP)
Subject
Nutrition and Dietetics,Medicine (miscellaneous)
Link
http://academic.oup.com/jn/article-pdf/133/1/38/24004340/4w0103000038.pdf
Reference66 articles.
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2. Identification of farnesol as the non-sterol derivative of mevalonic acid required for the accelerated degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase;Correll;J. Biol. Chem.,1994
3. Regulation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase degradation by the nonsterol mevalonate metabolite farnesol in vivo;Meigs;J. Biol. Chem.,1996
4. Suppression of mevalonate pathway activities by dietary isoprenoids: protective roles in cancer and cardiovascular disease;Elson;J. Nutr.,1995
5. Inhibition of hepatic cholesterol synthesis and S-3-hydroxy-3-methylglutaryl-CoA reductase by mono and bicyclic monoterpenes administered in vivo;Clegg;Biochem. Pharmacol.,1980
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