The relationship between microbial N synthesis and urinary excretion of purine derivatives in Dorper×thin-tailed Han crossbred sheep

2013 ◽  
Vol 112 (1-3) ◽  
pp. 49-55 ◽  
Author(s):  
Tao Ma ◽  
Kaidong Deng ◽  
Chenggang Jiang ◽  
Yan Tu ◽  
Naifeng Zhang ◽  
...  
Keyword(s):  
Urinary Excretion ◽  
Purine Derivatives ◽  
The Relationship ◽  
Microbial N

Urinary recovery of allantoin in normally fed steers

1998 ◽  
Vol 1998 ◽  
pp. 80-80
Author(s):  
F. Herrera Gomez ◽  
F. D. Deb Hovell ◽  
C. A. Sandoval Castro
Keyword(s):  
Urinary Excretion ◽  
Recovery Factor ◽  
Purine Derivatives ◽  
Urinary Recovery ◽  
Host Animal ◽  
N Supply ◽  
Normal Feeding ◽  
The Relationship ◽  
Infusion Technique ◽  
Microbial N

Studies in the use of the purine derivatives technique in ruminants have been stimulated by the possible use of this technique as an estimator of the rumen microbial-N supplied to the host animal. The recovery factor influences the estimation of the total purines absorbed and therefore the microbial-N supply. The relationship between exogenous purine input and urinary excretion and recovery has been studied using cattle maintained with the intragastric infusion technique (Orskov et al., 1979). The urinary recovery of exogenous purines has been estimated to be 0.77-0.85 (Chen et al., 1990a, Verbic et al., 1990), and this relationship has been assumed to be applicable to normal feeding situations. To our knowledge there is no data to support or reject this approach. This study examined the urinary recovery of exogenous allantoin input in steers under normal feeding conditions.

Urinary recovery of allantoin in normally fed steers

1998 ◽  
Vol 1998 ◽  
pp. 80-80
Author(s):  
F. Herrera Gomez ◽  
F. D. Deb Hovell ◽  
C. A. Sandoval Castro
Keyword(s):  
Urinary Excretion ◽  
Recovery Factor ◽  
Purine Derivatives ◽  
Urinary Recovery ◽  
Host Animal ◽  
N Supply ◽  
Normal Feeding ◽  
The Relationship ◽  
Infusion Technique ◽  
Microbial N

Studies in the use of the purine derivatives technique in ruminants have been stimulated by the possible use of this technique as an estimator of the rumen microbial-N supplied to the host animal. The recovery factor influences the estimation of the total purines absorbed and therefore the microbial-N supply. The relationship between exogenous purine input and urinary excretion and recovery has been studied using cattle maintained with the intragastric infusion technique (Orskov et al., 1979). The urinary recovery of exogenous purines has been estimated to be 0.77-0.85 (Chen et al., 1990a, Verbic et al., 1990), and this relationship has been assumed to be applicable to normal feeding situations. To our knowledge there is no data to support or reject this approach. This study examined the urinary recovery of exogenous allantoin input in steers under normal feeding conditions.

scholarly journals Determination of rumen microbial-nitrogen production in sheep: a comparison of urinary purine excretion with methods using 15N and purine bases as markers of microbial-nitrogen entering the duodenum

1996 ◽  
Vol 75 (5) ◽  
pp. 699-709 ◽  
Author(s):  
J. F. erez ◽  
J. Balcells ◽  
J. A. Guada ◽  
C. Castrillo
Keyword(s):  
Urinary Excretion ◽  
Basal Diet ◽  
Barley Grain ◽  
Rumen Content ◽  
Purine Derivatives ◽  
Flow Measurements ◽  
Mean Values ◽  
Purine Bases ◽  
Microbial Nitrogen ◽  
Microbial N

The present study compares estimates of rumen microbial-N production derived from duodenal flow measurements (15N and purine bases) with those from measurements of the urinary excretion of purine derivatives. Four Rasa Aragonesa ewes fitted with simple cannulas in the rumen and proximal duodenum were used. Four diets consisting of 550 g lucerne (Medicago sativa) hay/d as sole feed or supplemented with 220, 400 and 550 g rolled barley grain/d were given in a 4 x 4 random factorial arrangement. Duodenal digesta flows were determined by the dual-phase marker technique during continuous intraruminal infusions of Co-EDTA and Yb-acetate. Microbial contribution to the non-NH3N (NAN)flow was estimated from 15N enrichment and purines: N ratio in duodenal digesta and bacterial fractions isolated from the rumen content. Whole tract organic matter (OM) digestibility and duodenal flow of OM and NAN increased (P<0·001) with the level of barley supplementation. Digestible OM intake ranged from 19·0 to 42·7 g/kg metabolic weight (W0·75) and the duodenal flow of purine bases and the urinary excretion of allantoin increased Linearly (P < 0·001) from minimum values of 7·47 (SD 1·524)and 4·65 (SD 0·705) mmol/d respectively on the basal diet to 18·20 (SD 1·751) and 11·62 (SD 0·214) mmol/d on the 400 g barley diet; a further increase in barley supplementation decreased both variables (13/50 (SD 2/334) and 8/77 (SD 0/617) mmol/d respectively). Urinary excretion of uric acid and hypoxanthine showed a slight but significant increase (P < 0·05) over all levels of barley. Molar recoveries of duodenal purine bases as purine derivatives or allantoin in the urine were 0·78 (SD 0·156) and 0·65 (SD 0·130) respectively. The increase on barley supplementation significantly augmented microbial-N, but large differences between microbial markers employed were observed. Mean values of microbial-N estimated from the duodenal purine bases or urinary allantoin excretion were on average 18 and 29% lower than those measured by 15N.

Urinary purine derivatives excretion in Bos taurus and Bos indicus cattle

1998 ◽  
Vol 1998 ◽  
pp. 23-23
Author(s):  
F. Herrera Gomez ◽  
F.D.DeB Hovell ◽  
C.A. Sandoval Castro
Keyword(s):  
Small Intestine ◽  
Urinary Excretion ◽  
Bos Taurus ◽  
Bos Indicus ◽  
Purine Derivatives ◽  
Non Invasive ◽  
N Supply ◽  
Tropical Conditions ◽  
Invasive Method ◽  
Microbial N

The purine derivatives (PD) have been proposed as a non-invasive method to estimate microbial-N supply to the small intestine (Chen et al., 1990a; Verbic et al., 1990). The use of PD urinary excretion has the advantage that it can be used with intact animals thus reducing the concern of animal welfare issues. Although, there are known differences in purine metabolism between cattle (B. taurus), sheep and buffaloes (Bubalis bubalis) (Chen et al., 1990b; Chen et al., 1996), no direct comparison of PD urinary excretion has been made so far between cattle especies, therefore, the objective of the present experiment was to compare PD urinary excretion of B. taurus and B. indicus cattle fed similar diets under tropical conditions.

Rumen microbial production estimated either from urinary purine derivative excretion or from direct measurements of 15N and purine bases as microbial markers: effect of protein source and rumen bacteria isolates

1997 ◽  
Vol 65 (2) ◽  
pp. 225-236 ◽  
Author(s):  
J. F. Pérez ◽  
J. Balcells ◽  
J. A. Guada ◽  
C. Castrillo
Keyword(s):  
Organic Matter ◽  
Urinary Excretion ◽  
Fish Meal ◽  
Soya Bean ◽  
Purine Derivatives ◽  
Sunflower Meal ◽  
Purine Bases ◽  
Direct Measurements ◽  
Digestible Organic Matter ◽  
Microbial N

AbstractFour ewes fitted with ruminal and duodenal T-piece cannulae were each given six diets in a 6 × 4 factorial design. Diets or experimental treatments consisted of two ratios of forage: concentrate (700:150 (LC) and 400: 600 (HO). Forage was ammonia-treated straw and the concentrate was formulated with barley supplemented with one of three protein sources: sunflower meal, soya-bean meal or fish meal. Duodenal flows ofdigesta were estimated by the dual-phase technique using Co-EDTA and Yb acetate as liquid and solid markers. Microbial nitrogen (N) was estimated from the digesta flow of purine bases and 15N enrichment using as reference samples, bacterial isolates from the liquid (LAB) or solid (SAB) phase of rumen digesta.Duodenal flow of purine bases (mmol/day) was lower on LC (12·9) than HC (17·7) diets but in both treatments it was depressed by fish meal (12·3) compared with either soya-bean (17·3) or sunflower meal (16·3) as supplements (s.e. 1·13). Urinary excretion of purine derivatives showed a similar trend, 8·6 v. III mmol/day in LC and HC respectively and 8·8 v. 10·4 and 10·5 mmol/day in fish meal, soya-bean and sunflower meal diets (s.e. 0·56), respectively. Variation in excretion of urinary purine derivatives was mainly associated with digestible organic matter intake with an average ratio of 1·7 (s.e. 0·11) mmol per 100 g digestible organic matter intake. Irrespective of the microbial marker used, microbial yield was higher in animals offered HC than in those offered LC and with soya-bean or sunflower meal compared with fish meal supplemented diets. The microbial purine bases/N (mmol/g) ratio varied between LAB (1·99, s.e. 0·092) and SAB (1·69, s.e. 0·071) isolates leading to different estimates of microbial-N yield (g) from duodenal purine bases (7·76 (s.e. 2·84) v. 9·13 (s.e. 3·24)), urinary excretion of allantoin (5·57 (s.e. 2·0) v. 6·57 (s.e. 2·03)) or total purine derivatives (6·43 (s.e. 2·39) v. 7·56 (s.e. 2·77)). Urinary excretion of allantoin or total purine derivatives provided consistently lower estimates of duodenal microbial-N than duodenal purine bases or 15N, although it closely reflected the pattern observed in direct measurements.

scholarly journals Measurements of microbial N flow to the duodenum and urinary excretion of purine derivatives in bulls

1995 ◽  
Vol 44 (Suppl. 1) ◽  
pp. 177-177 ◽  
Author(s):  
Y. Beckers ◽  
A. Théwis ◽  
C. Sohy ◽  
E. François
Keyword(s):  
Urinary Excretion ◽  
Purine Derivatives ◽  
Microbial N

The effect of protein infusion on urinary excretion of purine derivatives in ruminants nourished by intragastric nutrition

1987 ◽  
Vol 109 (1) ◽  
pp. 7-12 ◽  
Author(s):  
T. Fujihara ◽  
E. R. Ørskov ◽  
P. J. Reeds ◽  
D. J. Kyle
Keyword(s):  
Uric Acid ◽  
Nucleic Acid ◽  
Urinary Excretion ◽  
Dietary Protein ◽  
The Other ◽  
Purine Derivatives ◽  
Average Recovery ◽  
Expected Values ◽  
The Relationship

SummaryTwo experiments were carried out to determine endogenous excretion of purine derivatives in steers and lambs, and to investigate the relationship between microbial nucleic acid input and urinary excretion of purine nitrogen.The endogenous excretion of allantoin after conversion of hypoxanthine, xanthine and uric acid to allantoin, was calculated to be 72 and 26 mg/kg W0·75 per day in steers and lambs, respectively, when the dietary protein contained no nucleic acid nitrogen.The excretion of purine derivatives increased linearly with increasing microbial nucleic acid input in lambs. The excretion of purine derivatives in excess of endogenous contribution was closely related to the theoretically expected values. The average recovery was calculated as 0·96 for one sheep and 1·0 for the other.

Urinary purine derivatives excretion in Bos taurus and Bos indicus cattle

1998 ◽  
Vol 1998 ◽  
pp. 23-23
Author(s):  
F. Herrera Gomez ◽  
F.D.DeB Hovell ◽  
C.A. Sandoval Castro
Keyword(s):  
Small Intestine ◽  
Urinary Excretion ◽  
Bos Taurus ◽  
Bos Indicus ◽  
Purine Derivatives ◽  
Non Invasive ◽  
N Supply ◽  
Tropical Conditions ◽  
Invasive Method ◽  
Microbial N

The purine derivatives (PD) have been proposed as a non-invasive method to estimate microbial-N supply to the small intestine (Chen et al., 1990a; Verbic et al., 1990). The use of PD urinary excretion has the advantage that it can be used with intact animals thus reducing the concern of animal welfare issues. Although, there are known differences in purine metabolism between cattle (B. taurus), sheep and buffaloes (Bubalis bubalis) (Chen et al., 1990b; Chen et al., 1996), no direct comparison of PD urinary excretion has been made so far between cattle especies, therefore, the objective of the present experiment was to compare PD urinary excretion of B. taurus and B. indicus cattle fed similar diets under tropical conditions.

Urinary excretion of allantoin and allantoin precursors by sheep after different rates of purine infusion into the duodenum

1991 ◽  
Vol 116 (2) ◽  
pp. 309-317 ◽  
Author(s):  
J. Balcells ◽  
J. A. Guada ◽  
C. Castrillo ◽  
J. Gasa
Keyword(s):  
Uric Acid ◽  
Urinary Excretion ◽  
Purine Derivatives ◽  
Urinary Recovery ◽  
Purine Derivative ◽  
Purine Bases ◽  
Proximal Duodenum ◽  
Maintenance Requirements ◽  
The Relationship ◽  
Energy Maintenance

SUMMARYTwo experiments were carried out to determine endogenous losses and the response of urinary purine derivatives to increased duodenal inputs of purine bases. Four ewes each fitted with a re-entrant cannula at the proximal duodenum, and conventionally fed, were subjected to full replacement of duodenal digesta followed by the administration of a solution either free of purines (Expt 1) or enriched with increasing amounts of purines, to supply 0·48–21·27 mmol/animal per day (Expt 2). Basal daily urinary excretions of allantoin, uric acid, hypoxanthine and xanthine were 11·5 ± 0·94, 9·9 ± 0·67, 6·9 ± 0·46 and 1·2 ±0·16 mg/kg W0·75. Allantoin was the only purine derivative which increased in response to incremental inputs of duodenal purines. The relationship between allantoin excretion and infused purines showed a urinary recovery of 0·8 for purines infused at > 220 μmol/kg W0·76. Lower rates of infusion did not alter allantoin excretion. The results show urinary allantoin to be a useful index to estimate duodenal input of purines when animals are fed close to or above their energy maintenance requirements.

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.

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