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Plasma triglyceride and low density lipoprotein metabolism
Author(s) -
CASLAKE M. J.,
PACKARD C. J.,
SERIES J. J.,
YIP B.,
DAGEN M. M.,
SHEPHERD J.
Publication year - 1992
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1111/j.1365-2362.1992.tb01942.x
Subject(s) - triglyceride , catabolism , medicine , apolipoprotein b , endocrinology , lipoprotein , low density lipoprotein , chemistry , metabolism , cholesterol , biology
. This study examines the relationship between plasma triglyceride and low density lipoprotein (LDL) levels by measuring the turnover of the native and 1,2 cyclohexanedione‐treated lipoprotein in 25 healthy adults. Plasma triglyceride showed a strong positive correlation with circulating LDL apoprotein (apo LDL) mass. In order to achieve a satisfactory fit to the kinetic data it was necessary to postulate the existence of two plasma apo LDL pools (A and B). When subjects were grouped in quintiles on the basis of circulating apo LDL mass, pool A predominated in those in the lowest quintile. The fractional catabolic rate (FCR) of apo LDL from this pool was high (FCR = 0.57 pM 0.06 pools day ‐1 ). As plasma triglyceride and apo LDL mass rose, apoprotein accumulated in the more slowly metabolized pool B as a result of an increase in the rate of input of apo LDL into the latter. The fractional clearance rate of protein from this pool remained unchanged at 0.26 pM 0.04 pools day ‐1 . Synthesis of apo LDL into pool B correlated with plasma triglyceride ( r = 0.553, P < 0.01), suggesting that the protein in this pool was derived from large, triglyceride‐rich very low density lipoprotein.