lipids Flashcards

1
Q

-building blocks of lipids
-hydrocarbon chains with a terminal coo-groups

A

Fatty Acids

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2
Q

-3 fatty acids molecules attached to one molecule of glycerol by ester bonds
-serves as main storage form of energy, insulator, shock absorber and integral part of cell membrane

A

TRYGLYCERIDES

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3
Q

-Similar to tryglycerides except that the third position on the glycerol backbone contaons a phospholipids head group
-contains polar and non-polar end
-constituent of cell membrane

A

PHOSPHOLIPIDS

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4
Q

Serve as part of cell membranes and as parent chain of cholesterol based hormones, e.g aldosterone, cortisol and the sex hormones
Exists in forms

A

CHOLESTEROL

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5
Q

App. 70% of TC

A

Cholesterol esters

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6
Q

app. 30% TC

A

Free Cholesterol

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7
Q

GENERAL LIPOPROTEIN STRUCTURE: Typical _________ in shape with sizes ranging from 10-1200 nm

A

SPHERICAL

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8
Q

GENERAL LIPOPROTEIN STRUCTURE: composed of lipids and proteins, called ______________

A

APOLIPOPROTEINS

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9
Q

GENERAL LIPOPROTEIN STRUCTURE: the various lipoproteins were originally separated through ______________

A

ULTRACENTRIFUGATION

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10
Q

-located on the structure of lipoprotein particles
-maintain structural integrity of lipoproteins
-serves as ligands for cell receptors

A

APOLIPOPROTEINS

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11
Q

TYPES OF MAJOR LIPOPROTEINS:
2nd largest, 2nd least dense
2nd highest TAG content
causes fasting hyperlipidemic turbidity

FUNCTION
transports endogenous (hepatic) tryglycerides

A

VLDL

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12
Q

TYPES OF MAJOR LIPOPROTEINS:
produced by the lipolysis of VLDL
small lipoprotein
directly related to risk of Coronary Heart disease
highest cholesterol content

FUNCTION
transport the Cholesterol to peripheral tissue

A

LDL-LOW DENSITY LIPOPROTEIN

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13
Q

TYPES OF MAJOR LIPOPROTEINS:
Smallest, but densest
highest protein content

FUNCTION
Reverse transport cholesterol

A

HDL-HIGH DENSITY LIPOPROTEIN

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14
Q

MINOR/ABNORMAL LIPOPROTEINS:
also known as FLOATING BETA-LIPOPROTEIN
seen in familial dysbetalipoproteinemia

A

BETA-VLDL

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15
Q

MINOR/ABNORMAL LIPOPROTEINS:
also known as sinking pre-beta lipoproteinemia
LDL-like particle

A

LP (A)

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16
Q

MINOR/ABNORMAL LIPOPROTEINS:
seen in biliary cholestasis, familial LCAT deficiency

A

LPX

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17
Q

BETA-VLDL is also known as?

A

FLOATING BETA-LIPOPROTEIN

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18
Q

SPECIMEN CONSIDERATION:
Fasting = _____ hrs

A

12 HOURS

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19
Q

CHOLESTEROL MEASUREMENTS:
Definitive method

A

ISOTOPE DILUTION MASS SPECTROMETRY (IDMS)

20
Q

glacial acetic acid
sulfuric acid
acetic anhydride

A

LIEBERMANN-BURCHARD REAGENT

21
Q

TRIGLYCERIDE MEASUREMENTS:
Hydrolysis of glycerol is accomplished using alcoholic KOH
Oxidation of glycerol by periodic acid, forming formaldehyde and formic acid
Formaldehyde combines with a variety of reagents:

A

CHEMICAL METHOD

22
Q

TRIGLYCERIDE MEASUREMENTS:
New reference method for triglyceride measurements, involve the hydrolysis of fatty acids on triglycerides and the measurement of glycerol.

A

GC-MS METHOD

23
Q

LIPOPROTEIN MEASUREMENTS:
Range in density observed among lipoprotein classes is a function of lipid and protein content and enables fractionation by density using centrifugation.

A

ULTRACENTRIFUGATION

24
Q

LIPOPROTEIN MEASUREMENTS:
Takes advantage of difference in size and change

A

ELECTROPHORESIS

25
Q

LIPOPROTEIN MEASUREMENTS:
Depends on particle size, charge and differences in the apolipoprotein content; primarily used in research labs only
Uses polyanions (heparin sulfate, dextran sulfate and phosphotungstate) and divalent cations such as magnesium, calcium and manganese e.g. HDL - dextran sulfate + magnesium

A

CHEMICAL PRECIPITATION

26
Q

LIPOPROTEIN MEASUREMENTS:
Uses antibodies specific to apolipoproteins to bind and separate lipoprotein classes.

A

IMMUNOASSAYS

27
Q

LIPOPROTEIN MEASUREMENTS:
Takes advantages of size differences in molecular sieving methods or composition in affinity methods e.g. gel chromatography or affinity chromatography.

A

CHROMATOGRAPHIC METHODS

28
Q

SUMMARY OF TEST AND END COLOR:
Liebermann-Burchardt reaction
end color - Cholestadienyl Monosulfonic Acid

A

GREEN COLOR

29
Q

SUMMARY OF TEST AND END COLOR:
Salkowski Reaction
end color - Cholestadienyl Disulfonic Acid

A

RED COLOR

30
Q

SUMMARY OF TEST AND END COLOR:
Abell, Levey and Brodie Mtd.

A

GREEN COLOR

31
Q

SUMMARY OF TEST AND END COLOR:
Van Handel and Zilversmith Mtd

A

BLUE COLOR COMPOUND

32
Q

(LDL-Cholesterol) = (total Cholesterol) - (HDL-C) - (Plasma TAG) / _______

A

2.175

33
Q

(LDL-Cholesterol) = (total Cholesterol) - (HDL-C) - (Plasma TAG) / 2.175

A

FRIEDWALD CALCULATION

34
Q

CLINICAL CORRELATIONS:
A narrowing and hardening of the arteries, caused by plaque formation, leading to reduced circulation.

A

ATHEROSCLEROSIS

35
Q

CLINICAL CORRELATIONS:
It is an autosomal dominant disorder caused by defective or deficient LDL receptors

A

FAMILIAL HYPERCHOLESTEROLEMIA (TYPE 2A)

36
Q

CLINICAL CORRELATIONS: Involves accumulation of plasma VLDL rich in cholesterol

A

FAMILIAL DYSBETALIPOPROTEINEMIA (TYPE 3 HYPERLIPOPROTEINEMIA)

37
Q

CLINICAL CORRELATIONS:
(Basses-Kornzweig Syndrome) defective apo B synthesis
Characterized by cerebellar ataxia, acanthocytosis, fat malabsorption

A

ABETALIPOPROTEINEMIA

38
Q

CLINICAL CORRELATIONS:
It is due to apo-B deficiency resulting from point mutation in apo-B
Decreased: LDL cholesterol and Total Cholesterol

A

HYPOBETALIPOPROTEINEMIA

39
Q

CLINICAL CORRELATIONS:
inherited disorder or lipid metabolism in which there are accumulation of sphingomyelin ib the bone marrow, spleen and lymph nodes.

A

NIEMANN-PICK DISEASE (LIPID STORAGE DISEASE)

40
Q

CLINICAL CORRELATIONS:
is a rare autosomal recessive disorder characterized by complete absence of HDL due to mutation.

A

TANGIER DISEASE

41
Q

CLINICAL CORRELATIONS:
It results to inability to clear chylomicron particles, creating the classic “type 1” chylomicronemia syndrome.

A

LIPOPROTEIN LIPASE DEFICIENCY

42
Q

CLINICAL CORRELATIONS:
Due to mutation in the LCAT gene
Fish-eye disease is milder form of LCAT deficiency

A

LCAT DEFICIENCY

43
Q

CLINICAL CORRELATIONS:
It is an inherited neurodegenerative disorder of lipid metabolism characterized by a deficiency of the enzyme hexosaminidase A, which results in the accumulation of sphingolipids in the brain

A

TAY-SACHS DISEASE

44
Q

CLINICAL CORRELATIONS:
This syndrome is distinct from abetalipoproteinemia, as only apob-48 appears to be affected.
Clinical finding: fat malabsorption and low levels of plasma lipids

A

CHYLOMICRON RETENTION DISEASE (ANDERSON’S DISEASE)

45
Q

CLINICAL CORRELATIONS:
It is a recessive disorder wherein plant sterols are absorbed and accumulate in plasma and peripheral tissues.

A

SITOSTEROLEMIA

46
Q

Other term for CHYLOMICRON RETENTION DISEASE

A

ANDERSON’S DISEASE

47
Q

Other term for CHYLOMICRON RETENTION DISEASE

A

ANDERSON’S DISEASE