Abstract
An in vitro model for the study of the catabolism of chylomicrons is suggested and characterized. The model utilizes the ability of perfused rat hearts to hydrolyze triglycerides of chylomicrons obtained from rat thoracic ducts. The resulting remnants were re-isolated and perfused through rat livers where the remnant lipid and protein was rapidly removed. In contrast intact chylomicrons were taken up by perfused liver to a limited extent. The remnants produced by cardiac perfusion contained a decreased percent of triglycerides and apoproteins C-2 and C-3, with a relative increase primarily in diglycerides and, to a lesser extent, monoglycerides and cholesterol. Most of the 125I-labelled remnant protein lost during hepatic perfusion was recovered in the tissue. The model thus simulated many of the known characteristics of chylomicron catabolism in vivo.
Original language | English |
---|---|
Pages (from-to) | 764-772 |
Number of pages | 9 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 63 |
Issue number | 3 |
DOIs | |
Publication status | Published - Apr 7 1975 |
Externally published | Yes |
Bibliographical note
Funding Information:ACKNOWLEDGEMENTS. This work was supported by grants from the Medical Research Council of Canada and the Quebec Heart Foundation. S-P. N. and P.J.D. were holders of an MRC Studentship and a CHF Fellowship, respectively.
ASJC Scopus Subject Areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology