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Papers In Press, published online ahead of print August 16, 2002
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Submitted on May 8, 2002
Biochemistry, University of Wisconsin-Madison, Madison, WI 53706
Corresponding Author: attie{at}biochem.wisc.edu
Stearoyl-CoA desaturase (SCD) is expressed at high levels in several human tissues and is required for the biosynthesis of oleate (18:1) and palmitoleate (16:1). These monounsaturated fatty acids are the major components of phospholipids, triglycerides, wax esters, and cholesterol esters. Mice with a targeted disruption of the SCD1 gene have very low levels of VLDL and impaired triglyceride and cholesterol ester biosynthesis. In the HYPLIP mouse, a model of hyperlipidemia, there was a four-fold increase in hepatic SCD activity, a 1.8-fold increase in the desaturation index, and a two-fold increase in plasma triglycerides. We used the plasma ratio of 18:1/18:0 (the “desaturation index”) as an in vivo measure of SCD activity in human subjects. In human subjects with triglycerides ranging from 0.3 to 20 mM, the desaturation ratio accounted for one-third of the variance in plasma triglyceride levels. A two-fold increase in the desaturation index was associated with a four-fold increase in plasma triglycerides. In human subjects exposed to a high carbohydrate diet, the desaturation index explained 44% of the variance in triglycerides. We propose that many of the factors that influence plasma triglyceride levels do so by converging upon the regulation of SCD activity.
Revised on July 1, 2002
Accepted on August 9, 2002
Relationship between stearoyl-CoA desaturase activity and plasma triglycerides in human and mouse hypertriglyceridemia
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