Role of apoproteins B and E in the receptor-mediated uptake of very-low-density lipoprotein remnants by the perfused rat liver

1985 ◽  
Vol 13 (1) ◽  
pp. 140-141 ◽  
Author(s):  
BHIM S. SURI ◽  
MICHAEL E. TARG ◽  
DONALD S. ROBINSON
Keyword(s):  
Rat Liver ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Very Low Density Lipoprotein ◽  
Low Density ◽  
Perfused Rat Liver

Concentration-dependent effects of eicosapentaenoic acid on very low density lipoprotein secretion by the isolated perfused rat liver

Lipids ◽  
1993 ◽  
Vol 28 (5) ◽  
pp. 419-425 ◽  
Author(s):  
Zu Jun Zhang ◽  
Henry G. Wilcox ◽  
Lawrence Castellani ◽  
Thomas V. Fungwe ◽  
Marshall B. Elam ◽  
...  
Keyword(s):  
Eicosapentaenoic Acid ◽  
Rat Liver ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Isolated Perfused Rat Liver ◽  
Very Low Density Lipoprotein ◽  
Low Density ◽  
Perfused Rat Liver ◽  
Lipoprotein Secretion

scholarly journals Effects of oleic acid on the biosynthesis of lipoprotein apoproteins and distribution into the very-low-density lipoprotein by the isolated perfused rat liver

1988 ◽  
Vol 251 (3) ◽  
pp. 809-816 ◽  
Author(s):  
W H Salam ◽  
H G Wilcox ◽  
M Heimberg
Keyword(s):  
Oleic Acid ◽  
Rat Liver ◽  
De Novo ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Isolated Perfused Rat Liver ◽  
Very Low Density Lipoprotein ◽  
Low Density ◽  
Perfused Rat Liver ◽  
Fasted Rats

The effects of oleic acid on the biosynthesis and secretion of VLDL (very-low-density-lipoprotein) apoproteins and lipids were investigated in isolated perfused rat liver. Protein synthesis was measured by the incorporation of L-[4,5-3H]leucine into the VLDL apoproteins (d less than 1.006) and into apolipoproteins of the whole perfusate (d less than 1.21). Oleate did not affect incorporation of [3H]leucine into total-perfusate or hepatic protein. The infusion of oleate, however, increased the mass and radioactivity of the VLDL apoprotein in proportion to the concentration of oleate infused. Uptake of oleate was similar with livers from fed or fasted animals. Fasting itself (24 h) decreased the net secretion and incorporation of [3H]leucine into total VLDL apoprotein and decreased the output of VLDL protein by the liver. A linear relationship existed between the output of VLDL triacylglycerol (mumol/h per g of liver) and secretion and/or synthesis of VLDL protein. Net output of VLDL cholesterol and phospholipid also increased linearly with VLDL-triacylglycerol output. Oleate stimulated incorporation of [3H]leucine into VLDL apo (apolipoprotein) E and apo C by livers from fed animals, and into VLDL apo Bh, B1, E and C by livers from fasted rats. The incorporation of [3H]leucine into individual apolipoproteins of the total perfusate lipoprotein (d less than 1.210 ultracentrifugal fraction) was not changed significantly by oleate during perfusion of livers from fed rats, suggesting that the synthesis de novo of each apolipoprotein was not stimulated by oleate. This is in contrast with that observed with livers from fasted rats, in which the synthesis of the total-perfusate lipoprotein (d less than 1.210 fraction) apo B, E and C was apparently stimulated by oleate. The observations with livers from fed rats suggest redistribution of radioactive apolipoproteins to the VLDL during or after the process of secretion, rather than an increase of apoprotein synthesis de novo. It appears, however, that the biosynthesis of apo B1, Bh, E and C was stimulated by oleic acid in livers from fasted rats. Since the incorporations of [3H]leucine into the VLDL and total-perfusate apolipoproteins were increased in fasted-rat liver when the fatty acid was infused, part of the apparent stimulated synthesis of the VLDL apoprotein may be in response to the increased formation and secretion of VLDL lipid.

Determinants of the uptake of very low density lipoprotein remnants by the perfused rat liver

Metabolism ◽  
1987 ◽  
Vol 36 (11) ◽  
pp. 1106-1113 ◽  
Author(s):  
Cynthia M. Arbeeny ◽  
Vincent A. Rifici ◽  
Dean A. Handley ◽  
Howard A. Eder
Keyword(s):  
Rat Liver ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Very Low Density Lipoprotein ◽  
Low Density ◽  
Perfused Rat Liver

scholarly journals A study of the interrelationship between the triacylglycerol and protein components of very-low-density lipoproteins using the perfused rat liver

1975 ◽  
Vol 150 (3) ◽  
pp. 315-321 ◽  
Author(s):  
S J Petersburg ◽  
A Madeley ◽  
D S Robinson
Keyword(s):  
Rat Liver ◽  
Low Density Lipoprotein ◽  
Polyacrylamide Gel Electrophoresis ◽  
Density Lipoprotein ◽  
Protein Release ◽  
Very Low Density Lipoprotein ◽  
Low Density ◽  
Perfused Rat Liver ◽  
Very Low Density Lipoproteins ◽  
Protein Components

High and low rates of very-low-density-lipoprotein triacylglycerol release from the perfused rat liver were achieved by using livers taken respectively from animals that had been given fructose for 48h or from animals that had been starved for 18h. 2. The higher rates of very-low-density-lipoprotein triacylglycerol release by the livers of the fructose-fed rats were associated with higher rates of very-low-density-lipoprotein protein release. 3. When the livers were perfused in the presence of [3H]leucine, radioactivity was incorporated into the very-low-density-lipoprotein apoproteins. The higher rates of very-low-density-lipoprotein triacylgycerol and protein release by the livers of fructose-fed rats were associated with a greater total incorporation of radioactivity into those apoproteins that entered the running gel during polyacrylamide-gel electrophoresis. However, the distribution of radioactivity among the various apoproteins was not significantly changed by the dietary treatments used.

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