Total cholesterol and cholesterol species analysis are critical in cardiovascular disease research. The protocol shows procedures that can be used for analysing tissue lipid extracts, lymph, bile or serum.
Method Article
Total Cholesterol and Cholesterol Species Determination
https://doi.org/10.1038/protex.2011.245
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posted 28 Jul, 2011
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Total cholesterol and cholesterol species analysis are critical in cardiovascular disease research. The protocol shows procedures that can be used for analysing tissue lipid extracts, lymph, bile or serum.
cholesterol
• Free cholesterol standard solution (1 mg/mL in ethanol)
• Cholesterol palmitate standard solution (1 mg/mL in chloroform): Add 106.383 mg of cholesterol palmitate (94%, Sigma) into a volumetric flask, top with chloroform.
• 33% KOH
• Ethanol
• Hexane
• O-phthalaldehyde in glacial acetic acid (50 mg/100mL)
Prepared freshly on the day of use
• Concentrated H2SO4
• Acetone-absolute ethanol (1:1, v/v)
• Acetone-anhydrous ether (1:2, v/v)
• Digitonin solution (0.5%): 100 mg digitonin/20 mL of 50 % ethanol (10 mL of D.I. water + 10 mL ethanol)
Make the digitonin solution just before analysis!
• Glacial acetic acid (10% in water): 1 mL of acetic acid in 9 mL of D.I. water
I. Total cholesterol analysis
• Prepare each set of 16x100 and 16x125 mm test tubes. Check the mouth of tubes.
• Check the accuracy of automatic pipettes and syringes.
• Evaporate the solvent under the N2 in a 40 C water bath.
• For lymph/bile/serum: vortex to homogenize the sample, use a 100 µL automatic pipette to add 100 µL of sample, and wash the tip with the same amount of D.I. water.
Use an automatic pipette to add 300 µL of KOH into the tube.
Use a 5 mL dispenser to add 3 mL of ethanol into the tube, cap it, and vortex it vigorously.
Saponify for 15 min in a 60 C water bath and let it cool.
Prepare o-phthalaldehyde solution during saponification.
Use a 5 mL dispenser to add 5 mL of hexane and vortex vigorously.
Use a 5 mL dispenser to add 1.5 mL of D.I. water and vortex vigorously.
Transfer the upper layer (lipid extracts) into a 16x125 mm disposable tube w/o cap, wash with 1.5 mL of hexane, combine the extracts and washings, and evaporate the solvent under the N2 in a 40 C water bath.
Use a 5 mL dispenser to add 3 mL of the o-phthalaldehyde solution into the tube and mix well.
Add 1.5 mL of concentrated H2SO4 by running down the inside wall of the tube and vortex well immediately.
II. Free cholesterol analysis
• Prepare 15 mL centrifuge tubes.
• Check the accuracy of automatic pipettes and syringes.
Add 1 mL of acetone-absolute ethanol (1:1) into a 15 mL plastic centrifuge tube. Cap the tube.
• For lymph/bile/serum: vortex to homogenize the sample, use a 100 µL automatic pipette to add 100 µL of sample, wipe the outside of the pipette tip with Kim-wipers, and wash the tip with acetone-absolute ethanol (1:1).
Use an automatic pipette to add 20 µL of glacial acetic acid solution (10%) into the tube.
Use an automatic pipette to add 500 µL of freshly made digitonin solution (10%) into the tube. Cap the tube and vortex vigorously.
Let the tube to stand at room temperature for 1 h.
Centrifuge the tube at 1000 x g for 20 min.
Use a Pasteur pipette to remove the supernatant (cholesterol esters) carefully without disturbing the precipitate.
Add 1 mL of acetone-ether (1:2) to the precipitate (free cholesterol). Cap the tube and vortex.
Centrifuge the tube at 1000 x g for 20 min.
Use a Pasteur pipette to remove the supernatant (cholesterol esters) carefully without disturbing the precipitate.
Dissolve the precipitate in 1 mL of ethanol. Vortex.
Transfer the mixture into a scintillation counting vial. Wash the centrifuge tube with 1 mL of ethanol.
Evaporate the solvent under N2 in a 40 C water bath.
Redissolve the free cholesterol in 100 µL of ethanol.
Add 10 mL of scintillation cocktail and count 14C in a liquid scintillation counter.
III. Principles
The system, LS6500, is designed for counting 14C, 3H, 32P, and other soft-beta emitters. Radioactive samples measured with an H-number are subjected to quench correction to determine actual sample activity, so called DPM, disintegrations per minute. The standard curve is plotted with the data from quenched standards with known activity containing the same type of isotope as in the sample and H-number are measured for each standard.
IV. Calculations
• % E (efficiency) = [(CPM-background)/DPM] x 100
Where,
% E is calculated from correction curve,
CPM is obtained in sample,
DPM is 3.92 x 104 [= (2.2 x 106 DPM/µCi) x (0.018 µCi)]
• Based on quench correction curve, %E is obtained to calculate DPM for any radioactive samples containing 14C.
• External standard curve: In order to plot standard curve for 14C, quenched standards with known activity were measured.
See figure in Figures section.Zou, W., Noh, S.K., Owen, K.O., & Koo, S.I. (2005) Dietary carnitine enhances the lymphatic absorption of fat and a-tocopherol in ovariectomized rats. J. Nutr. 135: 753-756.
"http://jn.nutrition.org/content/135/4/753.full":http://jn.nutrition.org/content/135/4/753.full
Rudel, L.L. & Morris, M.D. (1973) Determination of cholesterol using o-phthalaldehyde. J. Lipid Res. 14: 364-366.
Sperry, W.M. and Webb, M. (1950) A revision of the Scholenheimer-Sperry method for cholesterol determination. J. Biolo. Chem. 187: 97-100.
Wang, C.H., Willis, D.L. & Loveland, W.D. (1975) Radiotracer methodology in the biological environmental and physical sciences. Prentice-Hall, Inc. p. 181-199.
Thanks to Koo, S.I. for mentoring and financial supporting efforts.
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This protocol has been posted on Protocol Exchange, an open repository of community-contributed protocols sponsored by Nature Portfolio. These protocols are posted directly on the Protocol Exchange by authors and are made freely available to the scientific community for use and comment.
posted 28 Jul, 2011
You are reading this latest protocol version
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