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Cholesterol plasma

Familial lecithimcholesterol acyltransferase (LCAT) deficiency Absence of LCAT leads to block in reverse cholesterol transport. HDL remains as nascent disks incapable of taking up and esterifying cholesterol. Plasma concentrations of cholesteryl esters and lysolecithin are low. Present is an abnormal LDL fraction, lipoprotein X, found also in patients with cholestasis. VLDL is abnormal ( 3-VLDL). [Pg.228]

The nsnal reference is to plasma cholesterol, rather than blood cholesterol. Plasma is simply blood from which the blood cells (red cells, white cells, and platelets) have been removed. Since most clinical chemistry measnrements are made on plasma rather than blood, they are rightly reported as plasma valnes. If the plasma is permitted to clot and the clot removed, the resnlting hqnid is known as semm. [Pg.382]

The most common side effect associated with the use of nelfinavir is diarrhea other less frequent adverse effects include elevated triglycerides and cholesterol plasma levels, nausea, rash and hyperglycemia. [Pg.190]

The effect of oral barium exposure on various blood chemistry parameters that are important for cardiovascular function has been evaluated in only one experimental study with humans (Wones et al. 1990). In this study, 0.2 mg barium/kg/day as barium chloride was supplied in the drinking water of subjects for 4 weeks. No clinically significant changes were noted in any of the blood chemistry parameters monitored (total plasma cholesterol plasma triglycerides plasma HDL and LDL cholesterol plasma apolipoproteins and serum glucose, potassium, calcium, and albumin). [Pg.32]

Dietary MUFA have been found to have several positive effects that include, in addition to lowering human LDL-cholesterol plasma levels, positive effects on lipoprotein oxidation, coagulation, and fibrinolysis (29). Low-fat, monounsaturate-rich diets reduce the susceptibility of low-density lipoproteins to peroxidation ex vivo (30). In hypercholesterolemic subjects, diets containing MUFA resulted in favorable alterations in the fatty acid composition and oxidative profile of LDL in hypercholesterolemic subjects that were characterized as an increase in lipid peroxide lag time and a decrease in lipid peroxide formation (30). In animal studies. [Pg.555]

In addition, P-VLDL can also be observed directly by subjecting the VLDL fraction to agarose gel electrophoresis, where it migrates electrophoretically with LDL rather than VLDL (see Figure 26-26). The combination of a VLDL cholesterol/plasma triglyceride ratio of 0.3 or higher and the observation of p-VLDL in the ultracentrifugal supernatant establishes the type III lipoprotein pattern. [Pg.951]

Lovastatin and the other statins inhibit the rate-limiting step in cholesterol synthesis, HMG-CoA reductase. This lowers liver cholesterol, plasma LDL, and the hepatic synthesis of VLDL and apo B. [Pg.128]

High-Density Lipoprotein Cholesterol, Plasma Triglyceride, and Coronary Heart Disease Pathophysiology and Management Wolfgang Patsch and Antonio M. Gotto, Jr. [Pg.529]

Thyroid hormones regulate the turnover of carbohydrates, lipids, and proteins. They promote glucose absorption, hepatic and renal gluconeogenesis, hepatic glycogenolysis, and glucose utilization in muscle and adipose tissue (18). They increase de novo cholesterol synthesis but increase low-density lipoprotein degradation and cholesterol disposal even more, leading to a net decrease in total and in low-density lipoprotein cholesterol plasma levels (19). Thyroid hormones are anabolic when present at normal concentrations they then stimulate the expression of many key enzymes of metabolism. ... [Pg.1372]

Slowing, K., Ganado, P., Sanz, M, Ruiz, E., and Tejerina, T. 2001. Study of garlic extracts and fi actions on cholesterol plasma levels and vascular reactivity in cholesterol-fed rats. J Nutr 131(3s) 994S-999S. [Pg.455]

Hammache D, Pieroni G, Maresca M, Ivaldi S, YaM N, Fantini J. Reconstitution of sphingoUpad-cholesterol plasma membrane microdomains for studies of virus-glycolipid interactions. Methods Enzymol. 2000 312 495-506. [Pg.81]

The three main risk factors for CHD are smoking, hypertension and high plasma LDL-cholesterol plasma. [Pg.118]


See other pages where Cholesterol plasma is mentioned: [Pg.758]    [Pg.199]    [Pg.80]    [Pg.291]    [Pg.758]    [Pg.560]    [Pg.175]    [Pg.39]    [Pg.78]    [Pg.126]    [Pg.448]   
See also in sourсe #XX -- [ Pg.515 ]




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