Lipids and Laboratory Methods for Lipoproteins

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Comprehensive vocabulary flashcards covering lipid classifications, biochemistry, laboratory measurement methods, and associated clinical disorders based on the lecture material.

Last updated 10:49 AM on 8/6/26
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38 Terms

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Lipids

Primary source of fuel that provide stability to cell membranes and allow for transmembrane transport; they are insoluble in water but soluble in organic solvents like chloroform and ether.

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Lipoproteins

Spherical lipid and protein complexes with a liquid core of triglycerides and cholesterol esters and an outer shell of phospholipids, protein, and free cholesterol used to transport lipids in the blood.

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Fatty Acids

Short, medium, and long chains of molecules that serve as major constituents of triglycerides and phospholipids and provide a substance for gluconeogenesis.

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Saturated Fatty Acids

A type of fatty acid that acts as a building block for triglycerides and phospholipids and serves as a source of metabolic energy.

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Phospholipids

The most abundant lipid derived from phosphatidic acid, formed from two fatty acids and phosphorylated glycerol, creating an amphipathic molecule with polar and nonpolar ends.

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Sphingomyelin

An essential phospholipid component of the cell membranes of red blood cells and the nerve sheath.

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Lecithin (Phosphatidyl choline)

The most prevalent form of phospholipid in the body, accounting for 70% of total phospholipids.

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Surfactant

A substance composed of phospholipids that alters fluid surface tension in the alveolar space to prevent alveolar collapse during expiration.

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Neonatal Respiratory Distress Syndrome (RDS)

A condition caused by a deficiency of surfactant in newborns.

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Lecithin/Sphingomyelin (L/S) Ratio

A test used to estimate the status of fetal lung maturation by evaluating pulmonary surfactant in amniotic fluid.

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Cholesterol

An unsaturated steroid alcohol containing four rings and a single C−HC-H side chain; it is a vital structural component of cell membranes and a precursor of steroid hormones and bile acids.

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Cholesterol Esters (CE)

The neutral form of cholesterol bound to fatty acids, comprising 70% of total cholesterol, found in the center of lipid drops and lipoproteins.

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Free Cholesterol (FC)

A polar non-esterified alcohol comprising 30% of total cholesterol, available for membrane, hormone, and bile acid synthesis.

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Lecithin-Cholesterol Acyl Transferase (LCAT)

An enzyme that esterifies cholesterol in plasma by transferring fatty acids from lecithin to cholesterol.

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Acyl Cholesterol Acyl Transferase (ACAT)

A microsomal enzyme responsible for the re-esterification of excess cholesterol within cells.

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HMG-CoA reductase

The enzyme that reduces HMG−CoAHMG-CoA to mevalonate during the second stage of cholesterol biosynthesis.

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Salkowski Reaction

A chemical method for measuring cholesterol that produces a red colored end product called Cholestadienyl Disulfonic Acid.

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Liebermann-Burchardt Reaction

A chemical method for measuring cholesterol that produces a green colored end product called Cholestadienyl Monosulfonic Acid.

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Abell-Levy and Brodie Method

The CDC reference method for cholesterol measurement involving hydrolysis with alcoholic KOHKOH, hexane extraction, and colorimetry using L-B reagent.

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Triglycerides (Triacylglycerol)

The main storage lipid in humans, containing three molecules of fatty acids and one molecule of glycerol, providing insulation and energy.

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Chylomicrons (CM)

The largest and least dense lipoproteins (<0.95kg/L< 0.95 kg/L) produced in the intestine that deliver dietary lipids to hepatic and peripheral cells.

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VLDL (Very Low Density Lipoprotein)

Also known as pre-beta-lipoprotein, it is secreted by the liver to transport endogenous triglycerides to peripheral tissues.

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LDL (Low Density Lipoprotein)

Also known as beta-lipoprotein, it is the most atherogenic lipoprotein and the primary target of cholesterol-lowering therapy.

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HDL (High Density Lipoprotein)

Also known as alpha-lipoprotein, it is the smallest and most dense lipoprotein responsible for reverse cholesterol transport from tissues back to the liver.

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IDL (Intermediate Density Lipoprotein)

A product of VLDL catabolism, often called a VLDL remnant, that is eventually converted to LDL.

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Lipoprotein (a) [Lp(a)]

A 'sinking pre-B lipoprotein' variant of LDL that contains Apo (a) linked to Apo B−100B-100; it is an independent risk factor for atherosclerosis.

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Lipoprotein X (LpX)

An abnormal lipoprotein found in obstructive jaundice and LCAT deficiency, acting as a sensitive indicator of cholestasis.

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Apolipoprotein A-1

The major protein found in HDL that activates LCAT and is considered antiatherogenic.

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Apolipoprotein B-100

The major protein found in LDL, VLDL, and IDL, associated with an increased risk of coronary artery disease.

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Friedewald Equation

A formula used to calculate LDL cholesterol: LDLc=Totalcholesterol−(HDLc+VLDL)LDLc = Total cholesterol - (HDLc + VLDL), where VLDL=TG÷5VLDL = TG \div 5 in mg/dLmg/dL.

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DeLong Equation

An equation more accurate than Friedewald when triglycerides are above 400mg/dL400 mg/dL, where VLDL=TG÷6.5VLDL = TG \div 6.5.

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Standing Plasma Test

A screening test where plasma is refrigerated overnight; chylomicrons appear as a floating 'cream' layer, while excessive VLDL causes turbidity.

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Dyslipidemias

Diseases associated with abnormal lipoprotein levels, categorized into hyperlipoproteinemias (elevated) and hypolipoproteinemias (decreased).

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Tangier Disease

A hypolipoproteinemia characterized by the absence of HDL and very low levels of Apo A−IA-I and Apo A−IIA-II due to a mutation in the ABCA1ABCA1 gene.

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Abetalipoproteinemia

Also known as Bassen-Kornzweig syndrome, a condition where LDL and Apo B−100B-100 are absent, and triglycerides are nearly undetectable.

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Atherosclerosis

The narrowing of arteries due to plaque build-up on arterial walls caused by the deposition of cholesterol and triglycerides.

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Sitosterolemia

An extremely rare autosomal recessive disorder where plant sterols (phytosterols) are absorbed and accumulate in plasma and tissues.

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Chylomicron Retention Disease

Also known as Anderson's disease, it presents in childhood with fat malabsorption and low levels of plasma lipids.