scholarly journals Urinary excretion of purine derivatives and tissue xanthine oxidase (EC 1.2.3.2) activity in buffaloes (Bubalis bubalis) with special reference to differences between buffaloes and Bos taurus cattle

1996 ◽  
Vol 75 (3) ◽  
pp. 397-407 ◽  
Author(s):  
X. B. Chen ◽  
L. Samaraweera ◽  
D. J. Kyle ◽  
E. R. Ørskov ◽  
H. Abeygunawardene
Keyword(s):  
Uric Acid ◽  
Urinary Excretion ◽  
Xanthine Oxidase ◽  
Intestinal Mucosa ◽  
Bos Taurus ◽  
Purine Derivatives ◽  
Fresh Tissue ◽  
Creatinine Excretion ◽  
Digestible Organic Matter ◽  
Cattle And Sheep

AbstractThe urinary excretion of purine derivatives (PD) was measured in six buffaloes (Bubalis bubalis) during fasting and in fourteen buffaloes given four restricted levels of roughage (2·5-4·8 kg DM/d). Only allantoin and uric acid, not xanthine and hypoxanthine, were present in the urine, the pattern of excretion being similar to that in cattle. The fasting PD excretion amounted to 0·20 (SD 0·06) mmol/kg metabolic weight (W0·75) per d, and the rate of PD excretion as a linear function of feed intake was 5·2 mmol/kg digestible organic matter intake. Both values were considerably lower than the values for cattle reported in the literature. Creatinine excretion values were 0·33 (SD 0·06) and 0·44 (SD 0·09) mmol/kg W0.75 per d determined in fasting and feeding periods respectively. Fasting N excretion was 257 (SD 49) mg N/kg W0.75 per d. Both creatinine and fasting N excretions were also lower than in cattle. The activities of xanthine oxidase (EC 1.2.3.2) in plasma, liver and intestinal mucosa were determined in buffaloes, cattle and sheep. Xanthine oxidase activities in buffaloes were 24·5 (SD 2·7) unit/l plasma and 0·44 (SD 0·02) and 0·31 (SD 0·10) unit/g fresh tissue in liver and intestinal mucosa respectively. These activities were higher than those in cattle and sheep. Xanthine oxidase was practically absent from plasma and intestine of sheep. It is suggested that the differences in PD excretion between buffaloes and cattle were probably due to the smaller proportion of plasma PD that was disposed of in the urine of buffaloes.

scholarly journals Urinary excretion of purine derivatives as an index of microbial protein synthesis in the camel (Camelus dromedarius)

2004 ◽  
Vol 92 (2) ◽  
pp. 225-232 ◽  
Author(s):  
Abdelhai Guerouali ◽  
Youssef El Gass ◽  
Joaquim Balcells ◽  
Alvaro Belenguer ◽  
John Nolan
Keyword(s):  
Uric Acid ◽  
Urinary Excretion ◽  
Linear Increase ◽  
Camelus Dromedarius ◽  
Microbial Protein ◽  
Purine Derivatives ◽  
Fasting Period ◽  
Fresh Tissue ◽  
Digestible Organic Matter ◽  
Gut Mucosa

Five experiments were carried out to extend knowledge of purine metabolism in the camel (Camelus dromedarius) and to establish a model to enable microbial protein outflow from the forestomachs to be estimated from the urinary excretion of purine derivatives (PD; i.e. xanthine, hypoxanthine, uric acid, allantoin). In experiment 1, four camels were fasted for five consecutive days to enable endogenous PD excretion in urine to be determined. Total PD excretion decreased during the fasting period to 267 (se 41·5)?μmol/kg body weight (W)0·75 per d. Allantoin and xanthine+hypoxanthine were consistently 86 and 6·1?% of total urinary PD during this period but uric acid increased from 3·6?% to 7·4?%. Xanthine oxidase activity in tissues (experiment 2) was (μmol/min per g fresh tissue) 0·038 in liver and 0·005 in gut mucosa but was not detected in plasma. In experiment 3, the duodenal supply of yeast containing exogenous purines produced a linear increase in urinary PD excretion rate with the slope indicating that 0·63 was excreted in urine. After taking account of endogenous PD excretion, the relationship can be used to predict purine outflow from the rumen. From the latter prediction, and also the purine:protein ratio in bacteria determined in experiment 5, we predicted the net microbial outflow from the rumen. In experiment 4, with increasing food intake, the rate of PD excretion in the urine increased linearly by about 11·1?mmol PD/kg digestible organic matter intake (DOMI), equivalent to 95?g microbial protein/kg DOMI.

scholarly journals Urinary excretion of purine derivatives as an index of microbial-nitrogen intake in growing rabbits

1998 ◽  
Vol 79 (4) ◽  
pp. 373-380 ◽  
Author(s):  
J. Balcells ◽  
J. M. Ganuza ◽  
J. F. Pérez ◽  
S. M. Martín-Orúe ◽  
M. González Ronquillo
Keyword(s):  
Uric Acid ◽  
Urinary Excretion ◽  
Xanthine Oxidase ◽  
Live Weight ◽  
Jejunal Mucosa ◽  
Purine Derivatives ◽  
Fresh Tissue ◽  
Microbial Nitrogen ◽  
Se 33 ◽  
The Relationship

Three experiments were carried out to establish a response model between intake and urinary excretion of purine compounds. In Expt 1 the relationship between the intake of purine bases (PB) and the excretion of total purine derivatives (PD) was determined in seven growing rabbits with a mean initial live weight (LW) of 2·03 (SE 0·185) kg, aged 70 d, each fitted with a wooden neck collar to prevent caecotrophagy. They were fed on five experimental diets formulated with different levels of nucleic acids (0·00, 3·75, 7·50, 11·25, 15·00 g yeast-RNA/kg diet). The relationship between intake of purine (x,μmol/kg W0·75) and total urinary PD excretion (y,μmol/kg W0·75),y= 0·56 + 0·67x(r20·86; RSD 0·338), indicated that about 70% of duodenal PB were recovered as urinary PD and that the endogenous contribution was constant and independent of dietary PB supply. Endogenous excretion of PD (allantoin and uric acid) was measured in a second experiment using six rabbits fed on a purine-free diet and fitted with neck collars to avoid caecotrophagy. Basal daily urinary excretion values for allantoin and uric acid were 532 (SE 33·9) and 55 (SE 7·3) μmol/kg W0·75respectively; xanthine and hypoxanthine were not found in urine samples and therefore the sum of allantoin and uric acid should comprise the total excretion of PD (588 (SE 40·1) μmol/kg W0·75). The xanthine oxidase (EC 1·2.3·2) activity in plasma, liver, duodenum, jejunum and kidney was measured in a third experiment. The activities of xanthine oxidase in duodenal and jejunal mucosa, liver and kidney were: 0·61 (SE 0·095), 0·37 (SE 0·045), 0·035 (SE 0·001) and 0 units/g fresh tissue respectively and in plasma 2·96 (SE 0·094) units/1. The results show that urinary excretion of PD may be a useful tool to estimate duodenal PB input and microbial protein intake once the relationship between PB and N has been established in caecal micro-organisms.

Preliminary studies on urinary excretion of purine derivatives and creatinine in yaks

1999 ◽  
Vol 133 (4) ◽  
pp. 427-431 ◽  
Author(s):  
R. J. LONG ◽  
S. K. DONG ◽  
X. B. CHEN ◽  
E. R. ØRSKOV ◽  
Z. Z. HU
Keyword(s):  
Uric Acid ◽  
Urinary Excretion ◽  
Dry Matter ◽  
Field Experiments ◽  
Latin Square ◽  
Veterinary Science ◽  
Purine Derivatives ◽  
Digestible Organic Matter ◽  
Voluntary Intake ◽  
Energy Maintenance

Field experiments were conducted at the farm of Qinghai Academy of Animal and Veterinary Science, Xining, China during 1996/97 to determine the effects of level of food intake on the urinary excretion of purine derivatives (PD), creatinine and nitrogen in yaks (Bos grunniens). Two experiments were carried out with three female yaks (initial body weight 173–187 kg, age 5 years). For Expt 1 a 3×3 Latin square experimental design was used with three levels of oat hay (nitrogen 13·5 g/kg dry matter (DM)) intake treatments, i.e. 0·3, 0·6 and 0·9 of voluntary intake (1·3–3·5 kg DM/d). Each treatment lasted for 17 days and the samples were collected during the last 7 days of each period. For Expt 2 the animals were fed the same oat hay as in Expt 1 for 3 weeks at a level equivalent to the estimated energy maintenance requirement (M) (1·5–2·2 kg DM/d). The intake was then reduced to 0·6 M on day 1, 0·3 M on day 2 and zero from day 3 until day 10. The animals were re-fed in the reverse order for 3 days. Of the PD, only allantoin and uric acid were present in the urine. The proportions of allantoin and uric acid were 0·86 and 0·14 respectively for both experiments. There was no response of creatinine and nitrogen excretions to feed intake. The rates of PD excretion per kg digestible organic matter (DOM) or digestible dry matter (DDM) were 13·5 and 13·6 mmol respectively. As expected, urinary PD excretion increased significantly (P<0·001) with increasing intake of DDM and DOM. The daily fasting PD, creatinine and nitrogen excretions amounted to 0·22±0·02 (S.E.), 0·25±0·01 mmol/kg W0·75 and 314±24·2 mg/kg W0·75 respectively. The results suggest that it is possible to establish a method for estimating intestinal microbial protein flow based on PD excretion in yaks.

scholarly journals Excretion of purine derivatives by ruminants: endogenous excretion, differences between cattle and sheep

1990 ◽  
Vol 63 (1) ◽  
pp. 121-129 ◽  
Author(s):  
X. B. Chen ◽  
E. R. Ørskov ◽  
F. D. DeB. Hovell
Keyword(s):  
Uric Acid ◽  
Xanthine Oxidase ◽  
Oxidase Activity ◽  
Species Differences ◽  
Live Weight ◽  
Purine Derivatives ◽  
Purine Derivative ◽  
Xanthine Oxidase Activity ◽  
Milk Substitute ◽  
Cattle And Sheep

The endogenous urinary excretion of the purine derivatives allantoin, uric acid and xanthine plus hypoxanthine were measured in twenty-nine lambs, ten cattle (six steers, one cow and three preruminant calves) and four pigs. The sheep and mature cattle were nourished by intragastric infusion and the calves were given a milk-substitute. The pigs were fed on a purine-free diet. The excretion of total purine derivatives was substantially greater by the cattle, being 514 (se 20.6) μmol/kg live weight (W)0·75 per d compared with 168 (se 5·0) μmol/kg W0·75 per d by the sheep and 166 (se 2·6) μmol/kg W0·75 per d by the pigs. Plasma from normally fed sheep, cows and pigs was incubated with either xanthine or uric acid. Sheep and pig plasma had no xanthine oxidase (ec 1. 2. 3. 2) activity whereas plasma from cattle did. Uricase (ec 1. 7. 3. 3) was not present in plasma of cattle and pigs and appeared to be present in trace amounts only in sheep plasma. It is suggested that the species differences in endogenous purine derivative excretion were probably due to the different profiles of xanthine oxidase activity in tissues and particularly in the blood. This is because a high xanthine oxidase activity in tissues and particularly in the blood. This is because a high xanthine oxidase activity would reduce the chance to recycle purines, by increasing the probability of degradation to compounds which could not be salvaged.

scholarly journals Excretion of endogenous and exogenous purine derivatives in sheep: effect of increased concentrate intake

1998 ◽  
Vol 79 (3) ◽  
pp. 237-240 ◽  
Author(s):  
J. F. Pérez ◽  
J. Balcells ◽  
J. A. Cebrián ◽  
S. M. Martín-Orúe
Keyword(s):  
Organic Matter ◽  
Uric Acid ◽  
Urinary Excretion ◽  
Isotope Dilution ◽  
Basal Diet ◽  
Barley Grain ◽  
Dual Phase ◽  
Purine Derivatives ◽  
Marker System ◽  
Digestible Organic Matter

The present study examined the endogenous urinary excretion of purine derivatives (PD; allantoin, uric acid and xanthine plus hypoxanthine) in fed animals. Four Rasa Aragonesa ewes fitted with simple cannulas in the rumen and proximal duodenum were used. Animals were given a lucerne (Medicago sativa) hay diet, as sole feed (A) or supplemented, respectively, with 220 (B), 400 (C), and 550 (D) g rolled barley grain/d following a 4 × 4 random factorial design. Duodenal flow of purine bases (PB) was determined by the dual-phase marker system. 15N was infused continuously into the rumen to label exogenous or microbial PB. Duodenal PB flow and urinary excretion of PD increased with digestible organic matter intake showing a constant recovery of duodenal PB. The isotope dilution of PD in urine samples confirmed the presence of an endogenous fraction, originating from tissues, that increased from 115.2 (SE 5.84) μmol/kg W0.75 for the basal diet to 304.2 (SE 7.6) μmol/kg W0.75 at the highest level of duodenal PB.

scholarly journals Nitrogen balance in adult female mink (Mustela vison) in response to normal feeding andshort-term fasting

1997 ◽  
Vol 78 (1) ◽  
pp. 83-96 ◽  
Author(s):  
Anne-Helene Tauson ◽  
Jan Elnif ◽  
Søren Wamberg
Keyword(s):  
Urinary Excretion ◽  
Renal Clearance ◽  
Adult Female ◽  
Accurate Determination ◽  
Mustela Vison ◽  
Published Data ◽  
Purine Derivatives ◽  
Total N ◽  
Creatinine Excretion

Ten adult female mink (Mustela vison) were studied in a 7 d balance experiment consisting of a 2 d pre-surgery feeding period, followed by surgery, 1 d of recovery, 4 d of ad libitum feeding, and a 2d fasting period. In this experiment (Expt A) the animals had osmoticpumps implanted for continuous release of radioactively-labelled p–aminohippuric acid (p–aminobenzoyl-2-[3H]glycine; [3H]PAH;n10) and 14C-labelled inulin ([14C]IN; n 5). Repeated 24 h collections of urine, corrected to 100%[3H]PAH or [14C]IN recovery, were used for accurate determination of N balances, 24 h urinary excretion of urea, creatinine, and total N, and calculation of mean 24 h renal clearance rates for endogenous creatinine and inulin. N balances were slightly below zero, but not significantly different between feeding and fasting periods, indicating that correction to 100% [3H]PAH recovery resulted in slight overestimation of thefinal balances. During fasting, withdrawal of the dietary water and protein loads resulted in a dramatic decline in 24 h urinary volume, and urea and creatinine excretion. Large individualvariations in 24h urinary creatinine excretion (with relative variation coefficients up to 30%) confirmed that this is an unreliable index of the completeness of urine collection. In this respect, recovery rates of [3H]PAH proved far more consistent. Renal clearance values obtained in fed mink were in fair agreement with published data from cats, dogs and ferrets (Mustela putorius furo). Inulin clearance was about 30% higher than endogenous creatinine clearance, although its decline in response to fasting was not significant. In a separate study (Expt B)another ten female mink were equipped with osmotic pumps containing [3H]PAH for determination of 24 h excretion rates of purine derivatives. During feeding, allantoin accounted for more than 97 % of the excretion of purine derivatives in urine, uric acid making up less than 2·5%, xanthine and hypoxanthine less than 1 %. In fasted animals, urinary excretion of each of these purine derivatives declined to less than 50% of the feeding value. In conclusion, an experimental technique is presented for efficient and accurate measurements of daily urinary excretion of nitrogenous constituents, which allows for correct determination of N balances in adult mink and, presumably, in other mammalian species.

Basal urinary excretion of purine derivatives in sheep

1990 ◽  
Vol 1990 ◽  
pp. 109-109 ◽  
Author(s):  
J. Balcells ◽  
J.A. Guada ◽  
C. Castrillo ◽  
J.I. Bonafonte
Keyword(s):  
Uric Acid ◽  
Nucleic Acids ◽  
Urinary Excretion ◽  
Purine Derivatives ◽  
Exogenous Supply

In ruminants duodenal purines,mainly derived from microbial nucleic acids, are catabolised and excreted in the urine as xanthine, hypoxanthine, uric acid and allantoin. The use of purine derivatives as an index of net microbial syntesis in the rumen requires a better understanding of the contribution of endogenus losses to total urinary excretion.Similar levels of basal excretion of purine derivatives has been determined in ruminants maintained by intragastric nutrition (Giesecke et al. 1984, Fujihara et al. 1987) and preruminants fed on liquid diets (Linberg, 1989). However, lower excretion of allantoin and uric acid were recorded when exogenous supply was reduced by fasting (Rys et al. 1975).

Renal and salivary clearance of purine derivatives in sheep

1997 ◽  
Vol 65 (1) ◽  
pp. 83-91 ◽  
Author(s):  
J. C. Surra ◽  
J. A. Guada ◽  
J. Balcells ◽  
C. Castrillo
Keyword(s):  
Uric Acid ◽  
Plasma Concentration ◽  
Urinary Excretion ◽  
Buccal Cavity ◽  
Salivary Flow ◽  
Salivary Secretion ◽  
Purine Derivatives ◽  
Urinary Recovery ◽  
Fresh Matter ◽  
Saline Solutions

AbstractFour adult ewes (mean weight 42·6 kg) fitted with oesophageal fistulae were given 5 mmol/day ofallantoin or saline solutions by intrajugular continuous infusion. The experiment was a randomized cross-over design, with two consecutive 3-day infusion periods. One kg/day fresh matter of either chopped or pelleted fescue hay was distributed over 12 meals and salivary flow estimated from dilution of Co-EDTA infused into the buccal cavity. Allantoin infusion resulted in a rapid increase in its plasma concentration (84 to 128 (s.e. 1·5) μmol/l) and urinary excretion (9·6 to 13·3 (s.e. 0·18) mmol/day) without significant differences between diets. Salivary allantoin also increased (4·6 to 6·4 (s.e. 0·60) ymol/1) in response to infusion, although the concentration of total purine derivatives in saliva was only proportionately 0·08 that of plasma. Renal and salivary clearance of oxypurines, allantoin (78 (s.e. 5·0) ml/min and 13 (s.e. 0·7) ml/h), uric acid (466 (s.e. 98·0) ml/min and 45 (s.e. 9·8) ml/h) and creatinine (104 (s.e. 3·0) ml/min and 14 (s.e. 1·1) ml/h) were constant, irrespective of diet and infusion treatments. Urinary recovery of infused allantoin averaged 0·78 (s.e. 0·031) but salivary secretion, equivalent to about 0·003 of urinary losses, was not the explanation for the incomplete recovery.

scholarly journals Excretion of purine derivatives by ruminants: recycling of allantoin into the rumen via saliva and its fate in the gut

1990 ◽  
Vol 63 (2) ◽  
pp. 197-205 ◽  
Author(s):  
X. B. Chen ◽  
F. D. DeB. Hovell ◽  
E. R. ØRskov
Keyword(s):  
Fatty Acids ◽  
Uric Acid ◽  
Urinary Excretion ◽  
Volatile Fatty Acids ◽  
Rumen Fluid ◽  
Purine Derivatives ◽  
Complete Destruction ◽  
Series Of Experiments ◽  
Micro Organisms

The saliva of sheep was shown to contain significant concentrations of uric acid (16 (sd) 4.5) μmol/l) and allantoin (120 (sd 16.4) μmol/l), sufficient to recycle purine derivatives equivalent to about 0.10 of the normal urinary excretion. When allantoin was incubated in vitro in rumen fluid, it was degraded at a rate sufficient to ensure complete destruction of recycled allantoin. In a series of experiments in which allantoin was infused into the rumen of sheep fed normally, or into the rumen or abomasum of sheep and the rumen of cattle completely nourished by intragastric infusion of volatile fatty acids and casein, no additional allantoin was recovered in the urine. These losses were probably due to the degradation of allantoin by micro-organisms associated with the digestive tract. It is concluded that all allantoin and uric acid recycled to the rumen via saliva will be similarly degraded. Therefore, the use of urinary excretion of purine derivatives as an estimator of the rumen microbial biomass available to ruminants will need to be corrected for such losses.

Salivary losses of purine derivatives in sheep

1993 ◽  
Vol 1993 ◽  
pp. 176-176
Author(s):  
J. Surra ◽  
J.A. Guada ◽  
J. Balcells ◽  
C. Castrillo
Keyword(s):  
Uric Acid ◽  
Urinary Excretion ◽  
Salivary Secretion ◽  
Purine Derivatives ◽  
Preliminary Results ◽  
Ruminal Degradation ◽  
Saliva Flow

Developed models to estimate rumen microbial yield from the urinary excretion of purine derivatives fail to account for a complete absorbed purines (Chen et al., 1990a, Balcells et al., 1991). Ruminal degradation of purine derivatives recycled via saliva has been suggested as a possible explanation after detecting the presence of allantoin and uric acid in the sheep saliva (Chen et al. 1990b). However, it is not known to what extent these losses may be affected by dietary induced variations in saliva flow (Kay, 1966).This paper reports preliminary results of an experiment designed to study the effect of diet processing and blood allantoin concentration on the rate of purine derivatives losses through salivary secretion.

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