High-density lipoprotein inhibits the hydrolysis of Intralipid by human lipoprotein lipase

1985 ◽  
Vol 13 (1) ◽  
pp. 128-129 ◽  
Author(s):  
SHEELAGH M. A. JONES ◽  
M. PERENNA ROGERS
Keyword(s):  
High Density Lipoprotein ◽  
Lipoprotein Lipase ◽  
Density Lipoprotein ◽  
High Density ◽  
Hydrolysis Of

scholarly journals The effect in vitro of high-density lipoprotein on hydrolysis of triacylglycerol by lipoprotein lipase

1981 ◽  
Vol 200 (2) ◽  
pp. 453-456 ◽  
Author(s):  
M P Rogers ◽  
I Hutchinson
Keyword(s):  
Adipose Tissue ◽  
High Density Lipoprotein ◽  
Lipoprotein Lipase ◽  
Bovine Milk ◽  
Density Lipoprotein ◽  
High Density ◽  
Rat Adipose Tissue ◽  
Adipose Tissue Lipoprotein Lipase ◽  
Hydrolysis Of

In an incubation system in vitro with fully activated Intralipid as substrate, rat high-density lipoprotein inhibits the hydrolysis of triacylglycerol by lipoprotein lipase from rat adipose tissue, but does not inhibit hydrolysis by the enzyme from bovine milk. The pattern of inhibition suggests that substrate and high-density lipoprotein may compete for association with rat adipose-tissue lipoprotein lipase.

scholarly journals Effect of Thyroid Dysfunction on High-Density Lipoprotein Subfraction Metabolism: Roles of Hepatic Lipase and Cholesteryl Ester Transfer Protein1

1998 ◽  
Vol 83 (8) ◽  
pp. 2921-2924 ◽  
Author(s):  
K. C. B. Tan ◽  
S. W. M. Shiu ◽  
A. W. C. Kung.
Keyword(s):  
High Density Lipoprotein ◽  
Cholesteryl Ester ◽  
Lipoprotein Lipase ◽  
Thyroid Dysfunction ◽  
Hepatic Lipase ◽  
Density Lipoprotein ◽  
High Density ◽  
Free T4 ◽  
Hdl Metabolism ◽  
Hypothyroid Patients

abstract To investigate the effect of thyroid dysfunction on high-density lipoprotein (HDL) metabolism, we measured HDL subfractions, apolipoprotein A-I containing particles (LpA-I and LpA-I:A-II), and the activities of enzymes involved in the remodeling and metabolism of HDL[ namely hepatic lipase (HL), lipoprotein lipase, and cholesteryl ester transfer protein (CETP)] in 18 hyperthyroid and 17 hypothyroid patients before and after treatment. HDL was subfractionated by density gradient ultracentrifugation, and LpA-I was analyzed by electroimmunodiffusion. The major changes were found in the HDL2 subfraction and in LpA-I particles. HDL2-C and LpA-I were reduced in hyperthyroidism (P < 0.01, P < 0.05, respectively) and increased in hypothyroidism (both P < 0.05) compared with their respective euthyroid matched controls. Changes in HDL2-cholesterol were reversed after treatment in both hyper- and hypothyroid patients, and LpA-I also decreased in the hypothyroid patients after treatment. HL (P < 0.05) and CETP activities (P < 0.05) were elevated in hyperthyroidism and reduced in hypothyroidism (P < 0.05, P < 0.01 respectively) and both were related to free T4 levels. The changes in HDL2-C and LpA-I correlated significantly with changes in HL after treatment but not with CETP or lipoprotein lipase. In summary, HDL metabolism was altered in thyroid dysfunction, and the effect of thyroid hormone on HDL was mediated mainly via its effect on HL activity.

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