Regulation of cholesterol biosynthesis by diet in humans

被引:54
作者
Jones, PJH
机构
[1] Sch. of Dietetics and Human Nutri., Fac. of Agricultural and Envtl. Sci., McGill University, Ste-Anne-de-Bellevue, Que. H9X 3V9
关键词
cholesterol; biosynthesis; diet; food restriction; fat; plant sterols; mass isotopomer distribution analysis; deuterium incorporation;
D O I
10.1093/ajcn/66.2.438
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Biosynthesis of cholesterol represents a major input into whole-body pools; however, its regulation has been difficult to study in humans because of limitations in methodologies. The present objectives are to compare available techniques for measuring this process and examine how dietary factors alter human cholesterol biosynthesis. Review of existing techniques suggests that mass isotopomer distribution analysis and deuterium incorporation approaches offer advantages over other methods. Dietary factors influencing human cholesterol synthesis include energy restriction, meal frequency, dietary fat type, and cholesterol and phytosterol content. Food deprivation for as short as 24 h results in almost complete cessation of cholesterol biosynthesis. Similarly, increased meal frequency patterns are associated with a substantial depression in synthesis. In contrast, consumption of oils rich in polyunsaturated fatty acids. despite reducing circulating concentrations, increases the cholesterol synthesis rate compared with other fats. Stepwise addition of dietary cholesterol is associated with only a modest decline in cholesterogenesis while raising plasma concentrations slightly. It can be concluded that synthesis, as a contributor to circulating cholesterol concentrations, is sensitive to many dietary factors. Energy deprivation results in the greatest decline in synthesis, likely accounting for the beneficial decline in circulating cholesterol concentrations observed with weight loss.
引用
收藏
页码:438 / 446
页数:9
相关论文
共 85 条
[1]  
ANDERSEN JM, 1979, J LIPID RES, V20, P740
[2]   STEROL AND BILE ACID EXCRETION IN MAN AND EFFECTS OF DIETARY FAT [J].
AVIGAN, J ;
STEINBERG, D .
JOURNAL OF CLINICAL INVESTIGATION, 1965, 44 (11) :1845-+
[3]   TREATMENT OF SEVERE FAMILIAL HYPERCHOLESTEROLEMIA IN CHILDHOOD WITH SITOSTEROL AND SITOSTANOL [J].
BECKER, M ;
STAAB, D ;
VONBERGMANN, K .
JOURNAL OF PEDIATRICS, 1993, 122 (02) :292-296
[4]  
BJORKHEM I, 1987, J LIPID RES, V28, P1137
[5]   PRIMARY HYPERCHOLESTEROLEMIA - EFFECT OF TREATMENT ON SERUM-LIPIDS, LIPOPROTEIN FRACTIONS, CHOLESTEROL ABSORPTION, STEROL BALANCE, AND PLATELET-AGGREGATION [J].
BRIONES, ER ;
STEIGER, D ;
PALUMBO, PJ ;
KOTTKE, BA .
MAYO CLINIC PROCEEDINGS, 1984, 59 (04) :251-257
[6]   ASSAY OF HMG-COA REDUCTASE-ACTIVITY IN THE EVALUATION OF CHOLESTEROL-SYNTHESIS IN MAN [J].
CARULLI, N ;
TRIPODI, A ;
CARUBBI, F .
CLINICA CHIMICA ACTA, 1989, 183 (01) :77-81
[7]   LOW-DENSITY LIPOPROTEIN RECEPTOR ACTIVITY IN CULTURED HUMAN-SKIN FIBROBLASTS - MECHANISM OF INSULIN-INDUCED STIMULATION [J].
CHAIT, A ;
BIERMAN, EL ;
ALBERS, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1979, 64 (05) :1309-1319
[8]  
CLEEMAN JI, 1988, ARCH INTERN MED, V148, P36, DOI 10.1001/archinte.148.1.36
[9]   CHOLESTEROL BALANCE AND FECAL NEUTRAL STEROID AND BILE ACID EXCRETION IN NORMAL MEN FED DIETARY FATS OF DIFFERENT FATTY ACID COMPOSITION [J].
CONNOR, WE ;
WITIAK, DT ;
STONE, DB ;
ARMSTRONG, ML .
JOURNAL OF CLINICAL INVESTIGATION, 1969, 48 (08) :1363-+
[10]   EFFECTS OF INFANT NUTRITION ON CHOLESTEROL-SYNTHESIS RATES [J].
CRUZ, MLA ;
WONG, WW ;
MIMOUNI, F ;
HACHEY, DL ;
SETCHELL, KDR ;
KLEIN, PD ;
TSANG, RC .
PEDIATRIC RESEARCH, 1994, 35 (02) :135-140