Key result
Triton WR 1339 decreased phospholipid transfer to HDL (2.8% vs 10.1% in controls), whereas heparin increased it (12.6%), indicating lipolysis directly influences phospholipid transfer.
Absolute Event Rate: 2.8% vs 10.1%
Experimental lipolysis modulation alters HDL phospholipid transfer; leaves open its clinical relevance or therapeutic targeting in dyslipidemia.
The influence of lipolytic mechanisms on the transfer of phospholipids and unesterified cholesterol from artificial emulsions, serving as chylomicron models to other plasma lipoproteins, mainly high density lipoproteins (HDL) were tested in vivo. The emulsions labeled with radioactive lipids were injected into the bloodstream of rats (controls) and the results were compared with those obtained from rats that had previously been treated with Triton WR 1339 or heparin. Plasma clearance and the distribution of cholesteryl esters, phospholipids and unesterified cholesterol in the different plasma lipoprotein fractions were then determined. Whereas virtually no cholesteryl esters were found in d greater than 1.006 g/mL density fraction of the three experimental groups, 2.8 +/- 1.3% of the injected phospholipids were in the 1.063-1.210 g/L density fraction of the Triton treated rats, and 12.6 +/- 5.4% of the heparin treated rats, as compared to 10.1 +/- 1.7% in controls. This indicates that lipolysis directly influences phospholipid transfer to HDL. In contrast, free-cholesterol transfer to HDL, besides being less pronounced than phospholipid transfer, was enhanced by Triton and diminished by heparin, indicating that lipolytic mechanisms were not important determinants in this process.
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Maranhão et al. (1990) studied Lipid transfer. Triton WR 1339 or heparin vs. Control rats was evaluated on Phospholipid transfer to the 1.063-1.210 g/L density fraction (HDL). Triton WR 1339 decreased phospholipid transfer to HDL (2.8% vs 10.1% in controls), whereas heparin increased it (12.6%), indicating lipolysis directly influences phospholipid transfer.
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