MEASUREMENT OF ENDOGENOUS SYNTHESIS OF PLASMA-CHOLESTEROL IN RATS AND HUMANS USING MIDA

被引:73
作者
NEESE, RA
FAIX, D
KLETKE, C
WU, K
WANG, AC
SHACKLETON, CHL
HELLERSTEIN, MK
机构
[1] UNIV CALIF BERKELEY, DEPT NUTR SCI, BERKELEY, CA 94720 USA
[2] OAKLAND CHILDRENS MED CTR, CHILDRENS HOSP RES CTR, OAKLAND, CA 94609 USA
[3] UNIV CALIF SAN FRANCISCO, SAN FRANCISCO GEN HOSP, KORET CTR HUMAN NUTR, DEPT MED, SAN FRANCISCO, CA 94110 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 264卷 / 01期
关键词
CHOLESTEROGENESIS; MASS ISOTOPOMER DISTRIBUTION ANALYSIS; BIOSYNTHESIS; ACETYL-COENZYME-A; COMBUSTION-ISOTOPE RATIO MASS SPECTROMETRY; DIURNAL VARIATION;
D O I
10.1152/ajpendo.1993.264.1.E136
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We used the mass isotopomer distribution analysis (MIDA) technique to measure endogenous synthesis of plasma cholesterol in vivo in rats and normal human subjects. Sodium [1-C-13]- or [2-C-13]acetate was infused, and plasma free cholesterol was analyzed by gas chromatography-mass spectrometry. Frequencies of mass isotopomers M0-M4 (mass-to-charge ratio 368-372) were quantified. The enrichment of the true precursor for cholesterol synthesis (acetyl-coenzyme A in contributing tissues) was determined using the MIDA method. This technique remains mathematically valid even if more than one tissue contributes to circulating free cholesterol. The fractional contribution (f) from endogenous synthesis to free cholesterol in normal women (n = 5) was 2.48 +/- 0.39% after 7 h in the postabsorptive state and 1.27 +/- 0.41% after 8 h of refeeding. In ad libitum-fed rats (n = 12), f was 2.89 +/- 0.44% after 12 h, whereas administration of recombinant tumor necrosis factor increased this value fourfold. Next, the rate constant (k) for removal of labeled free cholesterol from plasma was calculated. Higher masses (M2-M4) were followed to avoid the problem of persistent label incorporation. During the 60 h after cessation of [C-13]acetate infusions, k was 0.02490 +/- 0.00298/h in humans. Using these values of k and f, absolute cholesterogenesis was 568 +/- 55 mg/day in normal women (follicular menstrual phase), similar to prior estimates based on whole body sterol balances. Women also exhibited a diurnal variation for endogenous cholesterol synthesis (34.6 +/- 5.4 mg/h nighttime vs. 15.9 +/- 5.2 mg/h daytime) consistent with current knowledge about rhythms in cholesterogenesis. Checks on the model were internally consistent (e.g., comparisons among different isotopomers for calculating precursor enrichment). We conclude that fractional and absolute endogenous cholesterol synthesis can be measured using stable isotopes in vivo by the MIDA technique.
引用
收藏
页码:E136 / E147
页数:12
相关论文
共 42 条
[1]   BIOLOGICAL SYNTHESIS OF CHOLESTEROL [J].
BLOCH, K .
SCIENCE, 1965, 150 (3692) :19-&
[2]   BODY CHOLESTEROL METABOLISM IN MAN .1. EQUILIBRATION OF SERUM AND TISSUE CHOLESTEROL [J].
CHOBANIAN, AV ;
HOLLANDER, W ;
SULLIVAN, M ;
COLOMBO, M .
JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (09) :1732-&
[3]  
DEINES P, 1980, HDB ENV ISOTOPE GEOC, V1, pCH9
[4]  
DIETSCHY JM, 1984, J LIPID RES, V25, P1469
[5]  
DIETSCHY JM, 1974, J BIOL CHEM, V249, P52
[6]   REGULATION OF CHOLESTEROL METABOLISM .2. [J].
DIETSCHY, JM ;
WILSON, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 282 (21) :1179-&
[7]  
DIETSCHY JM, 1974, J LIPID RES, V15, P508
[8]  
EDWARDS PA, 1972, J LIPID RES, V13, P396
[9]   TUMOR-NECROSIS-FACTOR-ALPHA STIMULATES HEPATIC LIPOGENESIS IN THE RAT INVIVO [J].
FEINGOLD, KR ;
GRUNFELD, C .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (01) :184-190
[10]   WHOLE-BODY AND HEPATIC CHOLESTEROL-SYNTHESIS RATES IN THE GUINEA-PIG - EFFECT OF DIETARY-FAT QUALITY [J].
FERNANDEZ, ML ;
YOUNT, NY ;
MCNAMARA, DJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1044 (03) :340-348