Chimeric molecules between human lipoprotein lipase (LPL) and rat hepatic lipase (HL) were used to identify structural elements responsible for functional differences. Based on the close sequence homology with pancreatic lipase, both LPL and HL are believed to have a two-domain structure composed of an aminoterminal (NHz-terminal) domain containing the catalytic Ser-His-Asp triad and a smaller ...

Adipose tissue lipoprotein lipase (LPL) is the enzyme responsible for hydrolysis of circulating lipoprotein triacylglycerol (TAG). Successive passages of very-low-density lipoprotein (VLDL) through adipose tissue are thought to produce progressive delipidation of the particles, with the eventual formation of intermediate-density lipoprotein (IDL) and low-density lipoprotein (LDL) [ 1 I . The hy...

1. Post-heparin lipolytic activity in man has been studied by using a triglyceride substrate emulsion containing different emulsifiers. 2. The lipolytic activity measured was profoundly influenced by the type of emulsifier used in the substrate. Substrate stabilized by synthetic emulsifiers give higher lipolytic activity than Intralipid, which contains egg phospholipids as emulsifiers. This dif...

Abhrak bhasma is a commonly used ayurvedic drug against many diseases including hepatitis. It is tested in albino rats using a model of hepatitis induced by a single dose of CCl4 (3 ml/kg body wt). Different doses of abhrak bhasma (10, 20, 30 and 40 mg/kg body wt) were tested to decide the dose related hepatoprotective efficacy. The centrolobular necrosis induced by single dose of CCl4 was redu...

An abnormal triglyceride-rich lipoprotein has been isolated from some patients with chronic renal failure or severe hypertriglyceridemia. The abnormal lipoprotein was characterized by an increased content of apolipoprotein (apo) C-III-2 (57.5% of total apo C-III peptides compared with 35.5% for controls, P less than 0.001) as characterized by isoelectric focusing and scanning densitometry. As d...

Lipoprotein lipase (LPL) is the rate-limiting enzyme for the hydrolysis of triglyceride-rich lipoproteins. Numerous LPL gene mutations have been described as a cause of familial chylomicronemia in various populations. In general, allelic heterogeneity is observed in LPL deficiency in different populations. However, a founder effect has been reported in certain populations, such as French Canadi...

TRIGLYCERIDE, phospholipid, and cholesterol absorbed from the intestines are transported in the blood stream in the form of chylomicrons and very low density lipoproteins (VLDL)." There is considerable evidence that triglyceride of chylomicrons and VLDL is hydrolyzed during uptake from blood and that this process is catalyzed by lipoprotein l ipase. * Lipoprotein lipase activity is found in tis...