Literature DB >> 4025547

Effect of lactation on cholesterol synthesis in rats.

K R Feingold, A H Moser.   

Abstract

Lactation induces a variety of morphological and functional changes in the gastrointestinal tract. In the present study we employed tritiated water as the substrate to demonstrate that in the intact rat lactation results in a twofold increase in cholesterol synthesis in the small intestine. Feeding a high-cholesterol diet did not markedly inhibit small intestinal cholesterol synthesis in either control or lactating animals, and the difference in cholesterol synthesis between the two groups persisted. In the large intestine, cholesterol synthesis is increased threefold in the lactating animals, and feeding a high-cholesterol diet did not affect synthesis in either the control or lactating animals. In the liver, lactation stimulated cholesterol synthesis, and quantitatively this increase in hepatic cholesterol synthesis is much greater than the increase observed in the intestines. Feeding the rats a high-cholesterol diet markedly inhibited hepatic cholesterol synthesis in both control and lactating animals, a finding that demonstrates that the feedback inhibition of cholesterol synthesis in the liver is not impaired by lactation. In the lactating animals, the quantity of labeled cholesterol in 1 ml of serum is 2.4 times greater than observed in controls. Feeding the rats a high-cholesterol diet markedly decreased the quantity of labeled cholesterol in the serum in both groups and obliterated the difference between control and lactating animals. This suggests that the increased hepatic cholesterol synthesis in the lactating animals is responsible for the differences in labeled cholesterol in the serum. Cholesterol feeding also reduced the quantity of labeled cholesterol localized to the mammary glands in lactating animals.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1985        PMID: 4025547     DOI: 10.1152/ajpgi.1985.249.2.G203

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  7 in total

1.  The inhibition of neutral cholesteryl ester hydrolase by a cytosolic protein factor in female rat liver: the influence of varying hormonal and nutritional conditions on the inhibitory activity.

Authors:  J H Shand; D W West
Journal:  Lipids       Date:  1992-06       Impact factor: 1.880

2.  ABCG5/ABCG8-independent biliary cholesterol excretion in lactating rats.

Authors:  Donna J Coy; Clavia R Wooton-Kee; Baoxiang Yan; Nadezhda Sabeva; Kai Su; Gregory Graf; Mary Vore
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2010-04-22       Impact factor: 4.052

3.  Mechanisms for increased expression of cholesterol 7alpha-hydroxylase (Cyp7a1) in lactating rats.

Authors:  Clavia Ruth Wooton-Kee; Donna J Coy; Antony T Athippozhy; Tianyong Zhao; Brett R Jones; Mary Vore
Journal:  Hepatology       Date:  2010-01       Impact factor: 17.425

4.  Tumor necrosis factor-alpha stimulates hepatic lipogenesis in the rat in vivo.

Authors:  K R Feingold; C Grunfeld
Journal:  J Clin Invest       Date:  1987-07       Impact factor: 14.808

5.  Role of reversible phosphorylation in mediating changes in the activity of hepatic 3-hydroxy-3-methylglutaryl-CoA reductase during pregnancy and lactation in the rat.

Authors:  R A Easom; V A Zammit
Journal:  Biochem J       Date:  1987-12-15       Impact factor: 3.857

6.  Differential gene expression in liver and small intestine from lactating rats compared to age-matched virgin controls detects increased mRNA of cholesterol biosynthetic genes.

Authors:  Antony Athippozhy; Liping Huang; Clavia Ruth Wooton-Kee; Tianyong Zhao; Paiboon Jungsuwadee; Arnold J Stromberg; Mary Vore
Journal:  BMC Genomics       Date:  2011-02-03       Impact factor: 3.969

7.  Milk cholesterol concentration in mice is not affected by high cholesterol diet- or genetically-induced hypercholesterolaemia.

Authors:  Lidiya G Dimova; Mirjam A M Lohuis; Vincent W Bloks; Uwe J F Tietge; Henkjan J Verkade
Journal:  Sci Rep       Date:  2018-06-11       Impact factor: 4.379

  7 in total

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