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PMID: 857111 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Relative utilization of fatty acids for synthesis of ketone bodies and complex lipids in the liver of developing rats.

Lipids ·Vol. 12 ·No. 4 ·1977-04-00 ·Pages 367-74

Yeh YY, Streuli VL, Zee P

Abstract

The regulation of hepatic ketogenesis, as related to the metabolism of fatty acids through oxidative and synthetic pathways, was studied in developing rats. [1-14C] palmitate was used as a substrate to determine the proportions of free fatty acids utilized for the production of ketone bodies, CO2 and complex lipids. Similar developmental patterns of hepatic ketogenesis were obtained by measuring the production of either [14C] acetoacetate from exogenous [1-14C] palmitate or the sum of unlabeled acetoacetate and beta-hydroxybutyrate from endogenous fatty acids. The production of total ketone bodies was low during the late fetal stage and at birth, but increased rapidly to a miximum value within 24 hr after brith. The maximal ketogenic capacity appeared to be maintained for the first 10 days of life. 14CO2 production from [1-14C] palmitate increased by two- to fourfold during the suckling period, from its initial low rate seen at birth. The capacity for synthesis of total complex lipids was low at birth and had increased by day 3 to a maximal value, which was comparable to that of adult fed rats. The high lipogenic capacity lasted throughout the remaining suckling period. When ketogenesis was inhibited by 4-pentenoic acid, the rate of synthesis of complex lipids did not increase despite an increase in unutilized fatty acids. During the mid-suckling period, approximately equal amounts of [1-14C] palmitate were utilized for the synthesis of ketone plus CO2 and for complex lipid synthesis. By contrast, in adult fed rats, the incorporation of fatty acids into complex lipids was four times higher than that of ketone plus CO2. These observations suggest that stimulated hepatic ketogenesis in suckling rats results from the rapid oxidation of fatty acids and consequent increased production of acetyl CoA, but not from impaired capacity for synthesis of complex lipids.

MeSH Terms
Acetoacetates/biosynthesis Aging Animals Cholesterol/biosynthesis Cholesterol Esters/biosynthesis Female Fetus Glycerides/biosynthesis Hydroxybutyrates/biosynthesis Ketone Bodies/biosynthesis Lipids/biosynthesis Liver/embryology,growth & development,metabolism Male Palmitic Acids/metabolism Phospholipids/biosynthesis Pregnancy Rats
Chemicals
Acetoacetates Cholesterol Esters Glycerides Hydroxybutyrates Ketone Bodies Lipids Palmitic Acids Phospholipids Cholesterol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yeh Y Y
Streuli V L
Zee P
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23 references, click to expand
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Article Info
Journal
Lipids
Abbr.
Lipids
ISSN
0024-4201
Published
1977-04-00
Pages
367-74
Language
English
Region
United States
NLM ID
0060450
Subset
IM
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