Literature DB >> 6481244

Age-related decreases in tissue sterol acquisition are mediated by changes in cholesterol synthesis and not low density lipoprotein uptake in the rat.

E F Stange, J M Dietschy.   

Abstract

The present investigation compared plasma cholesterol levels and lipoprotein profiles, and absolute rates of sterol synthesis and low density lipoprotein (LDL) uptake in various organs of immature (4 weeks old) and mature (15 weeks) rats. The plasma cholesterol level and its distribution among the major lipoprotein density fractions were similar in both groups. Using [3H]water as a substrate for measuring sterol synthesis in vivo, the content of newly synthesized cholesterol (3H-labeled digitonin-precipitable sterols; [3H]DPS) was several fold higher in all tissues of the young, compared to the old, rats when normalized per g of tissue. In contrast, whole-body [3H]DPS content was identical at 29.5 and 29.3 mumol/hr in young and old rats, respectively, despite a 4.4-fold difference in body weight (102 vs. 453 g). The importance of different organs to total-body sterol synthesis remained similar with increasing age although the skin (11 vs. 24% of total) rather than the small bowel (15 vs. 8%) became the second most important organ after the liver (49 vs. 45%) in the older animals. When LDL uptake was determined in these same organs, using constant infusion technique, the rates of clearance were higher only in the adrenal glands, adipose tissue, and skin of the young animals; whereas these rates were essentially the same in the liver and gastrointestinal tract, the two organs that are quantitatively most important for LDL catabolism. Even when these clearance rates were normalized to the whole organ or to 100 g of body weight, the differences in LDL uptake in the two age groups were minor compared to the major decrease in rates of cholesterol synthesis that were observed with aging. Finally, calculation of absolute rates of tissue cholesterol acquisition from both sources indicated that, in most organs, the majority of tissue cholesterol was derived from local synthesis rather than from LDL uptake in both age groups and that, with increasing age, total cholesterol acquisition decreased several-fold primarily as a consequence of the diminished rate of sterol synthesis. These studies demonstrate that with growth and aging in the rat there is a dramatic decrease in the rate of tissue cholesterol synthesis while the uptake of LDL-cholesterol remains essentially unchanged.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6481244

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  9 in total

1.  Kinetic constants for receptor-dependent and receptor-independent low density lipoprotein transport in the tissues of the rat and hamster.

Authors:  D K Spady; J B Meddings; J M Dietschy
Journal:  J Clin Invest       Date:  1986-05       Impact factor: 14.808

2.  Sterol synthesis and low density lipoprotein clearance in vivo in the pregnant rat, placenta, and fetus. Sources for tissue cholesterol during fetal development.

Authors:  W M Belknap; J M Dietschy
Journal:  J Clin Invest       Date:  1988-12       Impact factor: 14.808

3.  Mechanisms by which saturated triacylglycerols elevate the plasma low density lipoprotein-cholesterol concentration in hamsters. Differential effects of fatty acid chain length.

Authors:  L A Woollett; D K Spady; J M Dietschy
Journal:  J Clin Invest       Date:  1989-07       Impact factor: 14.808

4.  Age-related changes in catalytic activity, enzyme mass, mRNA, and subcellular distribution of hepatic neutral cholesterol ester hydrolase in female rats.

Authors:  R Natarajan; S Ghosh; W M Grogan
Journal:  Lipids       Date:  1997-05       Impact factor: 1.880

5.  Bezafibrate fails to directly modulate HMG-CoA reductase or LDL catabolism in human mononuclear cells.

Authors:  E F Stange; M Frühholz; M Osenbrügge; F Reimann; H Ditschuneit
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

6.  Contribution of newly synthesized cholesterol to rat plasma and bile determined by mass isotopomer distribution analysis: bile-salt flux promotes secretion of newly synthesized cholesterol into bile.

Authors:  R H Bandsma; F Stellaard; R J Vonk; G T Nagel; R A Neese; M K Hellerstein; F Kuipers
Journal:  Biochem J       Date:  1998-02-01       Impact factor: 3.857

7.  Age-related changes in the metabolism of cholesterol in rat liver microsomes.

Authors:  D Ståhlberg; B Angelin; K Einarsson
Journal:  Lipids       Date:  1991-05       Impact factor: 1.880

8.  The liver plays a key role in whole body sterol accretion of the neonatal Golden Syrian hamster.

Authors:  Lihang Yao; Paul S Horn; James E Heubi; Laura A Woollett
Journal:  Biochim Biophys Acta       Date:  2007-02-12

9.  Changes in ECG, plasma and myocardial lipids in experimental myocardial hypertrophy in rats.

Authors:  O Petkov; N Popova; V Orbetsova; R Kolarova; L Dakovska
Journal:  Basic Res Cardiol       Date:  1988 May-Jun       Impact factor: 17.165

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.