Volume 21, Issue 8 , Pages 736-740, August 2010
Plant sterol and stanol substrate specificity of pancreatic cholesterol esterase☆
Abstract
Consumption of plant sterols or stanols (collectively referred to as phytosterols) and their esters results in decreased low-density lipoprotein cholesterol, which is associated with decreased atherosclerotic risk. The mechanisms by which phytosterols impart their effects, however, are incompletely characterized. The objective of the present study is to determine if pancreatic cholesterol esterase (PCE; EC 3.1.1.13), the enzyme primarily responsible for cholesterol ester hydrolysis in the digestive tract, is capable of hydrolyzing various phytosterol esters and to compare the rates of sterol ester hydrolysis in vitro. We found that PCE hydrolyzes palmitate, oleate and stearate esters of cholesterol, stigmasterol, stigmastanol and sitosterol. Furthermore, we found that the rate of hydrolysis was dependent on both the sterol and the fatty acid moieties in the following order of rates of hydrolysis: cholesterol>(sitosterol=stigmastanol)>stigmasterol; oleate>(palmitate=stearate). The addition of free phytosterols to the system did not change hydrolytic activity of PCE, while addition of palmitate, oleate or stearate increased activity. Thus, PCE may play an important but discriminatory role in vivo in the liberation of free phytosterols to compete with cholesterol for micellar solubilization and absorption.
Keywords: Lipase, Phytosterols, Plant sterols, Plant stanols, Cholesterol metabolism, Cholesterol absorption
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☆ Grants, sponsors and funding sources: A.W.B. and J.H. were supported by USDA-NRI competitive grant no. 2007-35200-18298. The research was also supported in part by the University of Nebraska Agricultural Research Division with funds provided through the Hatch Act. Portions of this work were conducted in facilities remodeled with support from NIH (RR016544-01). NMR spectra were acquired, in part, on spectrometers purchased with NSF support (MRI 0079750 and CHE 0091975).
PII: S0955-2863(09)00101-6
doi:10.1016/j.jnutbio.2009.04.008
© 2010 Elsevier Inc. All rights reserved.
Volume 21, Issue 8 , Pages 736-740, August 2010
