Literature DB >> 1892876

Perinatal development of hepatic cholesterol synthesis in the rat.

N C Haave1, S M Innis.   

Abstract

Rates of cholesterol synthesis and HMG CoA reductase activity in rat liver, have been reported to be high before and low after birth. The timing of the decline in perinatal rates of cholesterol synthesis, however, is uncertain. These studies, therefore, determined in vivo rates of cholesterol synthesis using [3H]water and hepatic reductase activity in vitro in perinatal rats. The lipid composition of the plasma, liver and its microsomal subfraction were also determined. Reductase activity increased during late gestation, remained high immediately after birth, then decreased with the commencement of suckling. Rates of cholesterol synthesis increased from gestation day 18 to 20, but in contrast to reductase activity, decreased on the day before birth. Plasma cholesterol and triacylglycerol levels increased to gestation day 19, then decreased to term. By the 6th h after birth, plasma and liver cholesterol and triacylglycerol levels had increased markedly. By 48 h after birth, the high hepatic cholesterol content was associated with an increase in the cholesteryl ester fraction. The microsomal cholesterol/phospholipid molar ratio decreased from gestation day 16 until 12 h after birth, then increased markedly from 36 to 48 h. There was an apparent inverse relationship between the change in microsomal cholesterol/phospholipid molar ratio and the fatty acid unsaturation index from gestation day 16 to 36 h after birth. The results suggest that in late gestation and before suckling, the low in vivo rate of hepatic cholesterol synthesis may not be due to low activity of HMG CoA reductase.

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Year:  1991        PMID: 1892876     DOI: 10.1016/0005-2760(91)90229-b

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

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Journal:  Gene Expr       Date:  2018-06-21

2.  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

3.  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
  3 in total

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