Abstract

Livers from fasted or fed pigs were perfused for 5 h with Krebs-Ringer bicarbonate buffer containing human erythrocytes, bovine serum albumin, glucose, and amino acids. Liver viability was estimated by color, consistency, portal pressure, bile flow, electrolyte changes, and glucose levels in the perfusate, urea synthesis, [1-14C]leucine incorporation into protein, oxygen uptake, and histological examination. It was shown that the liver was maintained in good condition throughout the perfusions. The apolipoprotein B (apoB) and apolipoprotein A-I (apoA-I) in the perfusate were measured by solid phase radioimmunoassay. In the fasted state, the amount of apoB released was greatest in the low density lipoprotein (LDL) fraction and the amount was especially high during the 1st h. There was no increase of apoB in this fraction by feeding. The apoB in the very low density lipoprotein (VLDL) fraction was less than that in the LDL fraction in the fasted state, and it increased more than 2-fold in the fed animals. The amount of apoA-I was greatest in the 1.21 bottom fraction and was relatively small in the high density lipoprotein (HDL) fraction. The HDL fraction contained approximately one-twentieth as much apoA-I as the 1.21 bottom fraction in the fasted condition. In the fed state, apoA-I in the HDL fraction increased markedly, although the amount was still less than in the 1.21 bottom fraction.

Highlights

  • Livers from fasted or fed pigs were perfused for 5 h with Krebs-Ringer bicarbonate buffer containing human erythrocytes, bovine serum albumin, glucose, and amino acids

  • Utilizing a specific solid phase radioimmunoassay. apolipoprotein B (apoB) was detected in the very low density lipoprotein (VLDL), IDL, and low density lipoprotein (LDL) fractions isolated by sequential ultracentrifugation of the perfusate from fasted and fed livers

  • The greatest amount of apoB was found in the LDL fraction in the fasted animals and the mean values were slightly less in the fed condition, these differences were not statistically significant

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Summary

From the Division College of Medicine

The amount of apoB released was greatest in the low density lipoprotein (LDL) fraction and the amount was especially high during the 1st h. The apoB in the very low density lipoprotein (VLDL) fraction was less than that in the LDL fraction in the fasted state, and it increased more than Z-fold in the fed animals. There are species differences in the relative proportion of apoB in VLDL which appears in the circulating LDL fraction (X-17). Specific radioimmunoassays have been developed for measuring the synthesis and release of different apoproteins contained in the pig VLDL, LDL, and HDL. In this report we describe the development of the perfusion system and the results of our studies on the synthesis and release of apoB and apoA-I by the isolated perfused pig liver under fasting and fed conditions

Measurement of ApoB in Perfusate Lipoprotein
Lipoprotein fraction
DISCUSSION
Findings
Lipoprotein Synthesis by Perfused Pig Liver

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