CHAPTER 31: Interaction of Dietary Calcium with Genes of Transporters, Receptors and Enzymes Involved in Cholesterol Metabolism
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Published:06 Oct 2015
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X. Wang, L. Lei, Y. Liu, K. Y. Ma, J. Chen, R. Jiao, ... Z. Chen, in Calcium: Chemistry, Analysis, Function and Effects, ed. V. R. Preedy, The Royal Society of Chemistry, 2015, pp. 519-529.
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Dietary calcium has been shown to decrease plasma total cholesterol (TC) and low-density lipoprotein (LDL) cholesterol, particularly in postmenopausal women who have regularly taken calcium supplement for prevention of osteoporosis. Two possible mechanisms are associated with cholesterol-lowering activity of calcium supplement. First, calcium increases the bile-acid excretion due to its binding interaction with bile acids in the intestine. This is companied by upregulation of cholesterol-7α-hydroxylase (CYP7A1), a key enzyme in converting cholesterol to bile acids in the liver. Secondly, calcium supplement increases the cholesterol excretion, possibly mediated by downregulation of intestinal Niemann-Pick C1 like 1 (NPC1L1) and acyl coenzyme A: cholesterol acyltransferase 2 (ACAT-2), both of which are responsible for cholesterol absorption.