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Measurement of xanthine oxidase and uricase activity in plasma, liver and intestinal tissue
Objective
Outline of working
procedure
Sampling and preparation
of tissue extracts
Measurement of
xanthine oxidase activity
Measurement of
uricase activity
The objective is to provide some qualitative information about the tissue distribution of xanthine oxidase and uricase in the animals studied. The activities of xanthine oxidase in the intestine mucosa, the liver and blood affect the magnitude and pattern of PD excretion in the urine.
2. Outline of working procedure
1. Blood samples will be collected from at least 3 experimental animals of each species and assayed for enzyme activity within 2 h of collection.
2. Liver and intestinal tissue samples can be collected from a slaughter house from at least 3 different animals of the same species as the experimental animals. The tissue samples are kept in a polythene bag stored on ice, before assaying for enzyme activity, which should be carried out as quickly as possible.
3. Sampling and preparation of tissue extracts
Reagents
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0.05 M KH2PO4 (pH 7.5) |
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0.15 M KCl. |
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0.5 mM ethylenediaminetetracetic acid (EDTA) in 0.05 M KH2PO4 (pH 7.5). |
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0.05 M N-2-hydroxyethylpiperazine-N'-2-ethanesulphonic acid (HEPES) buffer (pH 7.5) containing 0.25 mM EDTA and 0.25 mM phenylmethylsulphonyl fluoride (PMSF). |
Equipment
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High speed centrifuge. |
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Glass tissue homogeniser with a Teflon pestle (e.g. Jencons 15-ml size, Cat. No 361092 or Fison TKW-300-030T or TWK-400-070K). |
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Dialysis (membrane) tubing (e.g. Visking, inflated diameter 19.0 mm, or Fison Cat. TWT-400 070M). |
Procedure
The procedure is a modification of the method by Furth-Walker & Amy [1].
Blood samples
1. Collect 20 ml of jugular blood into two 10-ml heparinised tubes.
2. Centrifuge at 2,500 g (4000 rpm) for 10 min at 4°C.
3. Use plasma for the assay within 2 h.
Liver samples
1. Collect 50-100 g of liver tissue (from animals in slaughter house). Transfer on ice to the laboratory as quickly as possible.
2. Wash in cold 0.15 M KCl, blot dry and freeze immediately if analysis is to be carried out on a different day.
3. Homogenise 1 g of liver in 9 ml of 0.5 mM EDTA in 0.05 M KH2PO4 (pH 7.5) in a glass homogenising tube with a Teflon pestle.
4. Centrifuge the extract at 40 000 g for 30 min at 4°C.
5. Dialyse the supernatant against the same EDTA-KH2PO4 buffer at 4°C for 24 h.
6. Centrifuge the contents of the dialysis bag at 40 000 g for 30 min at 4°C.
7. Use the supernatant for the assay. Store the supernatant at 4°C if the assay is to be carried out next day.
Intestinal tissue samples
1. Collect intestinal samples from a slaughter house. Take the first 30 cm segment of the small intestine.
2. Wash the lumen with cold 0.15 M KCl and then with 0.05 M HEPES buffer (pH 7.5) containing 0.25 mM EDTA and 0.25 mM PMSF.
3. Cut the segment of intestine length wise, open flat and scrape the mucosal surface carefully with a spatula in order to isolate the mucosal cells.
4. Homogenise 1 g of mucosal cells in 9 ml of the HEPES-EDTA-PMSF buffer, centrifuge the extract at 40 000 g for 30 min at 4°C.
5. Dialyse the supernatant at 4°C for 24 h against the HEPES-EDTA-PMSF buffer.
6. Centrifuge the contents of the dialysis tubing at 40 000 g for 30 min at 4°C.
7. Use the supernatant for the assay. Store the supernatant at 4°C if the assay is to be carried out next day.
4. Measurement of xanthine oxidase activity
The activity of xanthine oxidase (XO) is measured as the rate of uric acid production when xanthine is incubated with plasma or tissue extracts.
Reagents
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100 % (w/v) trichloroacetic acid (TCA). |
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0.05 M KH2PO4 (pH 7.5) buffer (adjust pH with KOH or H3PO4). |
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Substrate solution: 1.5 mM xanthine, 4.3 mM L-histidine and 1.0 mM potassium oxonate in 0.02 M NaOH. L-histidine is added to remove the possible inhibition of XO by excess xanthine [2] while potassium oxonate is added to inhibit uricase [3]. |
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Uric acid Standard solutions: 30 - 360 µM uric acid. |
Equipment
– Water bath.
– UV Spectrophotometer.
– High speed centrifuge.
Procedure
1. In test tubes, add 0.5 ml of blank or sample (plasma, liver or mucosa extract), 3 ml 0.05 M KH2PO4 (pH 7.5) buffer and 0.5 ml substrate solution. Use 0.5 ml of 0.05 M KH2PO4 (pH 7.5) as a blank for plasma sample, 0.5 ml 0.5 mM EDTA in 0.05 M KH2PO4 (pH 7.5) as a blank for liver samples and 0.5 ml of 0.05 M HEPES buffer (pH 7.5) containing 0.25 mM EDTA and 0.25 mM PMSF as a blank for intestinal samples. Analyse each sample in duplicate and also taken blank in duplicate (14 tubes are needed for each sample so that 2 tubes can be removed at 6 different times during incubation).
2. To two tubes, add 0.5 ml 100% (w/v) TCA and follow Steps 4 and 5.
3. Incubate the reaction mixture of other tubes at 37°C in water bath for up to 60 min. From the time of commencement of incubation, remove two tubes at 10 min intervals and terminate the reaction by addition of 0.5 ml 100% (w/v) TCA.
4. Centrifuge the mixture at 40 000 g for 30 min at 4°C.
5. Read absorbance of the supernatant at 292 nm.
Calculation
1. Establish a standard curve using uric acid standard solution in place of the sample. The absorbance (Y) vs concentration (X) relationship for uric acid may not be linear. Use a quadratic model (Y =AX2 + BX +C ) if not linear.
2. Calculate the amount of uric acid produced based on the uric acid standard curve, by solving the quadratic equation AX2 + BX + (C-Y) = 0
Describe the amount of uric acid produced (U µmol) as a mono-exponential
function of incubation time (t, min):
U = a + b (1-e-kt)
where ‘U’ is the cumulative production of uric acid (µmol),
‘a’ is the initial amount (µmol) of uric acid present in the
reaction system, ‘b’ the potential production of uric acid (µmol),
and ‘k’ the fractional rate of uric acid production.
3. Calculate the rate of uric acid production as b·k (µmol/min). One unit of XO activity is defined as 1 µmol uric acid produced per min at 37°C with excess substrate.
5. Measurement of uricase activity
The activity of uricase is measured as the rate of uric acid disappearance when uric acid is incubated with plasma or tissue extracts.
Reagents
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0.67 M pH 9.3 glycine buffer. |
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Uric acid solution: 357 µmol/L (60 mg/L) as substrate solution. |
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100% (w/v) trichloroacetic acid (TCA). |
Equipment
– Water bath.
– UV Spectrophotometer.
– High speed centrifuge.
– Eppendorf tubes.
Procedure
1. Mix 1 ml glycine buffer, 1 ml blank, plasma, liver or intestinal extracts and 0.5 ml uric acid substrate solution.
As a blank, use 0.05 M KH2PO4 (pH 7.5) for plasma samples, 0.5 mM ethylenediaminetetracetic acid (EDTA) in 0.05 M KH2PO4 (pH 7.5) for liver samples, 0.05 M N-2-hydroxyethylpiperazine-N'-2-ethanesulphonic acid (HEPES) buffer (pH 7.5) containing 0.25 mM EDTA and 0.25 mM phenylmethylsulphonyl fluoride (PMSF) for intestinal samples. Do each sample and blank in duplicate (14 tubes are needed for each sample so that 2 tubes can be removed at 6 different times during incubation).
2. To two tubes, add 0.5 ml 100% (w/v) TCA and follow Steps 4 and 5.
3. Incubate the reaction mixture of other tubes at 37°C in water bath for up to 6 h. From the time of commencement of incubation, remove two tubes at 1 h intervals and terminate the reaction by addition of 0.5 ml 100% (w/v) TCA.
4. Centrifuge the mixture at 40 000 g for 30 min at 4°C.
5. Read absorbance of the supernatant at 292 nm. Use uric acid ranging from 30-357 µmol/L (5-60 mg/L) as standards.
Note: This procedure has not been well tested and may need modification.
Calculation
It is the same as the calculation for xanthine oxidase activity described earlier. The uric acid content in the mixture decreases due to the presence of uricase.
REFERENCES
[1] FURTH-WALKER, D., AMY, N.K., Regulation of xanthine oxidase activity and immunologically detectable protein in rats in response to dietary protein and iron. J. Nutr. 117 (1987) 1697-1703.
[2] MURAOKA, S., Studies on xanthine oxidase 2. Biochimica et Biophysica Acta 73 (1963) 27-38.
[3] HASHIMOTO, S., A new spectrophotometric assay method of xanthine oxidase in crude tissue homogenate. Analytical Biochem. 62 (1974) 426-435.
[4] CHEN, X.B., ØRSKOV, E.R., HOVELL, F.D.DeB., Excretion of purine derivatives by ruminants: endogenous excretion, differences between cattle and sheep. Br. J. Nutr. 63 (1990) 121-129.
[5] CHEN, X.B., SAMARAWEERA, L., KYLE, D.J., ØRSKOV, E.R., ABEYGUNAWARDENE, H., Urinary excretion of purine derivatives and tissue xanthine oxidase activity in buffaloes, with special reference to differences between buffaloes and Bos taurus cattle. Br. J. Nutr. 75 (1996) 397-407.
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