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The incorporation of fatty acids of different chain length into liver and biliary lipids in the perfused rat liver
Authors:Moshe Rubin  Ronit Pakula  Tuvia Gilat  Alisa Tietz
Affiliation:(1) Felsenstein Medical Research Center, 49100 Petah-Tikva;(2) Sackler Faculty of Medicine’ Minerva Center for Cholesterol Gallstones and Lipid Metabolism in the Liver, Tel Aviv University, 64239 Tel Aviv;(3) Department of Gastroenterology, Tel Aviv Medical Center, 64239 Tel Aviv;(4) Department of Neurobiochemistry, Tel Aviv University, Tel Aviv, Israel;(5) Department of Surgery “B”, Beilinson Medical Center, 49100 Petah Tiqva, Israel
Abstract:In an attempt to correlate the incorporation of fatty acids (FA) of different chain length into liver and biliary lipids’ isolated rat livers were perfused for 2 h with Krebs-Ringer bicarbonate containing 1% albumin and 10 μmol of [1-14C]-labeled FA: C2’ C8’ C10’ C12’ C16’ and C18∶1. One to 1.36 μmol of medium-chain fatty acids (MCFA’ C8’ C10’ and C12) and 6.6 μmol of long-chain FA (LCFA) were incorporated into liver lipids’ 40% of the latter into phosphatidylcholine (PC). 14C-acetate (13 nmol) was incorporated into biliary cholesterol; 14C-MCFA contributed only 3.2–5 nmol; LCFA did not lead to newly synthesized cholesterol. Newly synthesized liver PC (2.75 to 3.25%) and newly synthesized liver cholesterol (6.5 to 10%) were secreted into bile. The specific radioactivity of biliary PC after infusion of all-saturated FA was 3.8–6.8 times higher than that of liver PC; for C18∶1 it was only 1.7-fold. The specific radioactivity of biliary cholesterol’ as compared to liver cholesterol’ was 12 times higher for C2 and five times higher for MCFA. This indicates that a considerable proportion of the newly synthesized lipids was secreted into bile prior to significant mixing with preexisting liver PC and cholesterol pools. liver PC contained 8% of unchanged 14C−C12; while 14C−C10 was not detected. Biliary PC’ in contrast’ contained 18% of unchanged 14C−C12 and 3% 14C−C10. These results suggest that after prolonged infusion of medium-chain triacylglycerols/longchain triacylglycerols to patients’ biliary PC may become enriched with MCFA. In addition’ the oxidation of these FA may provide C-2 units which increase cholesterol synthesis.
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