Plant-Derived Monoterpenes Suppress Hamster Kidney Cell 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Synthesis at the Post-Transcriptional Level

Author:

Peffley Dennis M.1,Gayen Apurba K.2

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)

Reference66 articles.

1. Non-sterol compounds that regulate cholesterogenesis. Analogues of farnesyl pyrophosphate reduce 3-hydroxy-3-methylglutaryl-coenzyme A reductase levels;Bradfute;J. Biol. Chem.,1994

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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