Urea utilization in growing lambs. 6. N balance with 15N urea

Lambs of an age of 2 or 4 months and of an average live weight of 14.7 and 27.4 kg resp. received rations consisting of 44% cereals, 46% dried sugar beet pulp, 6% wheat starch, 2% urea and 2% mineral-vitamin mixture. The crude protein content was 17.1 and 15.9% resp. in the dry matter, that of native crude protein 10.6 and 9.4% resp. During a 6-day N balance period 8 and 16 g 15N urea resp. with a 15N excess (15N') of 9.26 and 9.40 atom-% were fed orally instead of commercial feeding urea. There were no significant differences between the two age groups with regard to the digestibility of the organic matter and the crude nutrients. The average N balance of 372 +/- 85 mg/kg LW 0.75/day were in the intermediate range of N retention capacity and accounted for 26 +/- 5% of the consumed N. N retention in per cent. was slightly lower in younger lambs. Projections of urea utilization in a quasi stationary state resulted in an efficiency of the utilization of 33 +/- 4%. The dismembering of the lambs at the end of the main period showed between 0.02 and 0.22 atom-% 15N' in the total N, TCA precipitable N and amino acid N of the meat. At between 0.24 and 0.38 atom-% 15N' they were highest in the heart and jaw muscles. The quota of 15N' amounts found in the total N of the meat were 10.6 +/- 3% of the 15N-intake and 20.1 +/- 5.1% of the 15N' amount remaining in the body. The bones contained 7.7 +/- 1.7% and the fleece 7.9 +/- 3.1% of the 15N'-intake. Generally seen, the total N and urea utilization was slightly lower in younger lambs than in older ones.     

The effect of energy concentration and source on the use of feed protein and NPN in lambs. 3. Allantoin excretion and microbial protein synthesis

In an N balance experiment with male crossbreeding lambs at an age of 3 ... 4 months four different rations were given differing in energy concentration (high greater than 700 EFU cattle/kg DM and low less than 650 EFU cattle/kg DM) and in the energy source (sugar, starch or crude fibre) with crude protein intake being almost equal. The rations contained 2% urea. Microbial protein synthesis in the rumen was assessed according to ROTH and KIRCHGESSNER (1978) (1), RYS et al. (1975) (2) and BICKEL-BAUMANN and LANDIS (1986) (3) on the basis of allantoin excretion in urine. The highest ruminal protein synthesis quotas were 868 ... 921 mg protein N per kg LW0.75 in (2). In (3) 723 ... 766 mg protein N/kg LW0.75 were synthesized. From the 15N labelling of the supplemented urea and the excreted allantoin it could be calculated that 26 ... 40% of the microbial protein resulted from the urea-N of the ration. Despite a high crude protein content of the ration of between 16 and 17% in the DM and a relation of NPN: pure protein of 0.95 the utilization of the NPN in the ration was relatively high but slightly lower than the utilization of pure protein. The variants with higher energy concentration showed as a tendency higher allantoin excretion in spite of slightly lower dry matter intake and a slightly higher NPN utilization than the variants with lower energy concentration.     

Utilization of 15N-labelled urea by laying hens. 1. Survey of the literature, 15N-excretion in feces and urine

Three colostomated leghorn hybrids with an average laying performance of 75% received a ration with 17.7% crude protein and an energy content of 519 energetic feed units for hens per kg mixed feed over a period of 8 days. In the first six days of the experiment the 1%-supplement of urea to the ration was labelled. Its atom-% 15N excess (15N') amounted to 96.06%. During the last two days the urea supplement was not labelled. The total N, trichloracetic acid (TCA)-soluble N and the ammonia N were determined in the feces samples collected daily. In the urine samples collected daily the total N, urea N and ammonia N per hen were determined as well. In all samples the atom-% 15N excess (15N') was measured. The percentage of 14N in feces of the 14N dose was, on an average of the three hens, 21.3% and the analogous quota of 15N' 4.6%. The quota of ammonia 14N of the total 14N in feces had an average of 2.5%, the corresponding 15N' quota was 10.1%. The atom-% 15N' of the urea N in urine was considerably above that of the total urine N and had a maximum of more than 50%. The quota of urine 14N of the 14N taken in had an average of 44.4%, and the corresponding 15N' quota was 56.9%. On an average of the three hens, 61.6% of the 15N' were excreted in feces and urine during the 8-day test period.     

The determination of a gross utilization of 15N-lysine in laboratory rats. 1. Experiment with normal intestinal flora (without antibiotic supplement)]

Wistar rats of a live weight of about 100 g were divided into 14 groups (5 animals/group). The rations given supplied the animals with 75%, 100% and 125% lysine, which brought about a moderate growth of the animals of approximately 2 g/animal and day achieved by limited feeding. The 3 lysine levels mentioned could be achieved by lysine supplements (L-lysine-HCl) for the following rations: barley (B), wheat (W), and wheat gluten (WG). For isolated soybean protein (assay protein) (S) the lysine levels 100% and 125% and for soybean meal (SM) the levels 116% and 125% could only be achieved. A control group with whole egg ration (W) (with its natural lysine content of 125% of the requirement) were also tested as comparison. During the 10-day period of the main experiment all 14 rations were supplemented with 0.5 g 15N-lysine (alpha amino group, 95% labelled with 15N). The N balance could only be significantly improved by lysine supplements in the rations B, W and SM with the lysine level of 125%. The biologic value of the protein sources was in rations B and WG also significantly improved by the highest lysine supplement. 15N excess (15N') from the deaminated 15N lysine was excreted with diet B rich in crude fibre mainly in faeces (more than 15% of the intake) and only about 10% in urine. With the diets without native crude fibre the excretion quota changed in favour of urine. The following 15N' amounts in per cent of 15N' intake from lysine were excreted in urine and faeces: B 75 = 31.3, B 100 = 30.9, B 125 = 28.0, W 75 = 24.3, W 100 = 32.2, W 125 = 32.6, GW 75 = 18.3, WG 100 = 24.2, WG 125 = 28.1, S 100 = 39.4, S 125 = 50.4, SM 116 = 34.9, SM 125 = 32.9, W 125 = 19.1. 15N excretion in urine and faeces increased in comparable relations in 6 cases of lysine increase levels only. Gross utilization of lysine can only conditionally be quantified by 15N labelled lysine supplement.     

Utilization of 15N marked urea by the laying hen. 2. Incorporation and metabolism of 15N for the synthesis of egg protein

In an N-metabolism experiment 3 colostomized laying hybrids received 2870 mg 15N-excess (15N') per animal in 6 days in the form of urea with their conventional feed rations. During the 8-day experiment the 21 eggs laid were separated into eggshell, white of egg and yolk. Weight, N-content and 15N' were determined of the individual fractions of the eggs. On an average of the 21 eggs 4.6% of the heavy nitrogen was in the egg-shells, 50% in the white of egg and 45.5% in the yolk. 2.8%, 4.5% and 5.5% (hens 1...3) of the 15N' consumed were detected in the eggs. The maximum 15N'-output in the white of egg was reached on the 6th day, whereas 15N'-output in the yolk showed a nearly linear increase in the time of the experiment. The results show that labelled nitrogen from urea is incorporated into the egg to a lower degree than after the feeding of 15N-labelled proteins and that the development of its incorporation into the white of egg and the yolk differ from that after the feeding of 15N-labelled native proteins.     

Utilization of 15N-labeled urea in laying hens. 9. Bones, feathers and 15N-incorporation in the rest of the body

For studying the incorporation of the 15N labelled urea into individual organs and tissues 3 colostomized laying hens were butchered after they had received 1% urea (96.06 atom-% 15N excess) with a high quality ration over a period of six days and after receiving conventional urea for another two days. Nitrogen and atom-% 15N excess (15N') were determined in the bones, the feathers and the remaining body (skin, lungs and windpipe, head with comb and wattle, lower leg without bones and with skin, pancreas and fatty tissue). In the remaining body the atom-% 15N' was determined in 15 amino acids. The labelling in the remaining body and the bones was approximately the same and averaged 0.37 atom-% 15N'. A significantly lower relative frequency could be detected in the feathers. The lysine of the remaining body contained only 0.04 atom-% 15N', tyrosine 0.06, histidine and arginine 0.07. The phenylalanine and proline molecules were labelled with 0.11 atom-% 15N'. Most 15N' was incorporated in serine and glutamic acid with over 0.30 atom-%. In the six non-essential amino acids out of the 15 amino acids studied, 48.6 of the non isotopic nitrogen of the total N of the remaining body and 70.7% of the isotopic nitrogen of total 15N' could be detected. Consequently the urea-N is mainly used for the synthesis of the non-essential amino acids, with its utilization being very low.     

Nutrition physiology effects of dietary fats in rations for growing pigs. 5. Effects of soy bean oil and lard on protein retention in piglets

In two experiments with 30 and 26 castrated male pigs of the German Landrace breed, weight range 15-30 kg, the influence of isoenergetic changes in the carbohydrate and fat fractions of the diet were examined. The effect of the addition of soya oil (SO) and lard (LA) to the diet on the utilization of protein and on the blood urea concentration was also examined. The apparent digestibilities of the crude nutrients and energy were determined using different methods. The following were examined: experiment I: ration I (control), ration II (+7% SO), ration III (+7% LA) experiment II: ration I (control), ration II (+2% SO), ration III (+2% SO + 5% LA), ration IV (+7% LA) In all experiments the animals were fed a similar amount of digestible crude protein of constant quality at constant ME-intake. In both experiments the apparent digestibility of crude protein in the groups with 7% added fat was 4% higher (p less than 0,05) than in the corresponding control groups. The apparent digestibility of crude fat in experiment I and II (in groups II and III and in groups III and IV, respectively) was approximately 87%, when calculated on the basis of faecal fat which was determined by a simple ether extract procedure. When the faeces was treated with HCl before determination, these values for experiment I and II were approximately 6% (p less than 0,001) and 1% (NS) lower, respectively. In both experiments the utilization of protein and the blood urea concentration were not significantly influenced by the amount or form of fat included in the rations.     

Dynamics of amino acid and protein metabolism of laying hens after the administration of 15N-labeled wheat protein. 3. Incorporation of 15N into egg shell, egg white and egg yolk

12 colostomized laying hybrids received a ration meeting their requirement of 15N labelled wheat with a 15N excess (15N') of 14.37 atom-% over 4 days. The 15N' of the total ration amounted to 4.47 atom-%. Each hen consumed 135 mg 15N' per day. On another 4 days the same rations with non labelled wheat were fed. The 12 hens laid 56 eggs during the 8 days of the experiment. They were divided into egg shell, white and yolk of egg. In addition, the protein of the white and yolk of egg was precipitated with trichloric acetic acid (TCA) and the nitrogen in these fractions was determined. On average of the 56 eggs, the N quota in the egg shell was 5.3%, in the white of egg 49.1% and in the yolk 45.6%. The atom-% 15N' in the shells of the eggs laid on the first day of the experiment was on average 0.21, whereas only 0.03 and 0.02 atom-% 15N' resp. could be detected in the white and yolks of the eggs. On the first day after the last 15N application the atom-% 15N' in the egg shell and the white of egg was highest and amounted to 2.33 and 2.43 atom-% resp. The highest value of 1.83 atom-% 15N' in the yolk was ascertained 3 days after the last 15N intake. The mean quota of TCA-precipitable N in the white of egg is 97.6% and in the yolk 94.4% of the respective total N. The atom-% 15N' in the non-protein N-compounds was higher than in the protein fractions.     

糊化淀粉尿素对山羊消化代谢和增重的效果

选择３６只本地白山羊随机分成３组进行饲养试验。配制３种分别含有豆粕、糊化淀粉尿素和尿素并达到等能等氮水平的混合材料，定量饲喂，干草自由采食。３５天饲养试验后，每组选３只阉公羊作上述３种日粮的消化代谢试验。结果表明：（１）３种日粮的粗纤维表现消化率分别为６４．６５±５．５８％、６６．１０±３．７２％和６１．４９±７．６１％。（２）３种日粮的氮代谢率分别为２５．８３±４．８６％、２２．２５±７．０％和１９．３６±３．９８％，糊化淀粉尿素日粮比尿素日粮提高１４．９３％。（３）与尿素日粮相比，动物采食含糊化淀粉尿素日粮后外周血液尿素浓度有所下降，且动态变化也相对平稳。（４）３个日粮组的日增重分别为６８．４５±３５．８４、７０．８３±３１．２８和６１．９１±３１．８０ｇ／只，差异不显著（Ｐ＞０．０５）；每千克增重所需日粮粗蛋白质分别为９２６．５、９５２．２和１１３３．２ｇ，尿素日粮的饲喂效果最差。结果分析指出：糊化淀粉尿素产品能有效改善尿素氮的利用率，并能达到与豆粕相同的增重效果。     

The effect of a straw meal on the crude protein and amino acid metabolism and digestibility of the crude nutrients in broiler hen breeds. 2. Digestibility of crude nutrients of rations and 15N from a straw meal and wheat

In experiments with colostomized broiler hens apparent digestibility of the crude nutrients of the ration after straw meal supplements of 20, 30 and 40 g per animal was determined. In addition, the 15N digestibility of straw meal and wheat was ascertained on the basis of straw meal supplements. The digestibility of the crude nutrients of the rations decreased significantly (P less than 0.05) after the straw meal supplement. The adaptation of the test animals to the straw meal intake resulted, at a daily consumption of 20 g straw meal, in an increase of the apparent crude fat digestibility (P less than 0.05) in dependence on the time of straw meal feeding, in which the original values without straw meal supplement were not reached. The digestibility of the 15N excess (15N') of the wheat was, at 86 +/- 1%, largely independent of the straw meal intake. The apparent digestibility of the straw-15N excess in broiler hens of 42 +/- 8 to 55 +/- 2% is surprisingly high.     

Investigations of the influence of the content of plant crude protein in the ration on the utilisation of urea in dairy cattle. 5. 15N-fractions in the blood of lactating cows given 15N-urea intraruminantly

The incorporation of urea-15N (given as an intraruminal drench or infusion) into plasma urea and protein of dairy cows fed isoenergetic rations with different levels of plant protein (9, 11, 12, 14, 15 and 17% in DM) was investigated. A nonlinear and asymptotic dependence between the plasma concentration of urea and protein level in the ration was stated. The availability of dietary urea-15N for plasma urea for 48 hours after administration was lowest in cows fed with low protein rations (9 and 11% of plant protein). On the contrary the highest incorporation of urea-15N into plasma protein of these animals was observed. The possible explanation of these results is presented.     

The Diurnal Variation of Urea in Cow’s Milk and how Milk Fat Content,Storage and Preservation Affects Analysis by a Flow Injection Technique

Six Swedish Red and White dairy cows, producing 20-39 kg of 4% fat-corrected milk were given a ration balanced in energy and protein. They had access to feed from 05.15 to 09.00 and from 13.00 to 16.30 and were milked at 06.15 and 15.30. The milk was analysed for urea with a FIA technique.There was a significant diurnal variation in milk urea. The highest values were found 3–5 h after the beginning of the morning feeding and the lowest values (down to 60% of the max. values) during late night. Within 1 h after the start of the morning feeding the urea values had increased significantly, but they had decreased within the same time after the start of the afternoon feeding. Since there was a pronounced diurnal variation in the milk fat content, the urea concentration was also recalculated to concentration in the water phase of the milk. It was higher in that phase, but the pattern of the diurnal variation was not changed significantly. However, analyses on milk with a very high fat content may give misleading results.There were no important differences in the milk urea concentration of different udder quarters. When calculated as concentration in the water phase of the milk, no differences in urea concentration were found between the beginning and the end of milking. The analytical method had a good precision (coefficient of variation max. 3%). The milk urea concentration was not changed significantly after storage during 10 days at 4°C when no preservative was added; but after 17 days the milk had turned sour and the urea value had increased. When a preservative (bronopole) was added the urea concentration remained unchanged during 17 days. Deepfreezing did not influence the urea concentration.     

Utilization of N15-labelled urea in the laying hen. 6. Incorporation in the liver and kidneys

In an experiment 3 colostomized laying hybrids received a normal ration containing 1% 15N labelled urea with 96.06% atom-% 15N excess (15N') over six days. Subsequently the same ration with unlabelled urea was given over 2 days, after which the animals were butchered. In the kidneys the 15N' amounted to 1.1 atom-% and 1.8 atom-% in the liver. The TCA soluble N fraction and the ammonia were more highly labelled than the total N. Lysine, histidine and arginine were lowly labelled in the kidneys. This also applies to the liver with the exception of histidine. In the branch-chained and aromatic amino acids of the liver the 15N' was between 0.2 and 0.3 atom-%. The highest labelling of non-essential amino acids was found in glutamic acid with 0.9 atom-% 15N' and aspartic acid with 1.1 atom-% 15N'. The evaluation of the amino acid in the liver showed that the 6 non-essential amino acids account for two thirds of the total amino acid 15N' whereas the 9 essential ones account for one third of the amino acid 15N' only.     

Experimental Trials Assessed by Two Different Protein Evaluation Systems

Carlsson, J., and B. Pehrson: The influence of the dietary balance between energy and protein on milk urea concentration. Experimental trials assessed by two different protein evaluation systems. Acta vet. scand. 1994, 35, 193-205.–Twentythree dairy cows were fed rations with different proportions of energy and digestible crude protein (DCP). When the ration was balanced for energy and DCP according to Swedish standard the cows’ milk urea concentration was 4.66-4.92 mmol/1 (95% CI of mean). With increasing intakes of DCP, fed together with standard levels of energy, the mean milk urea concentration increased in proportion to the surplus of DCP. In contrast, the concentration of urea decreased when the cows were overfed with energy at the same time as they were underfed with protein.When the rations were recalculated in accordance with the AAT/PBV system for dietary protein evaluation the 95% CI for the mean milk urea concentration of the cows receiving a balanced ration was 3.76-4.56 mmol/1. The concentration of urea was dependent primarily on the PBV. When the 2 protein evaluation systems were compared there was a strong correlation between PBV and DCP. Ammonia was the only constituent of the rumen whose concentration was strongly correlated with the milk urea concentration.Taken together with earlier data the present results suggest that a milk urea concentration between 4.0 and 5.5 mmol/1 should be regarded as normal at least when cows are fed conventional feedstuffs.     

Nutritional-physiological effects of dietary fats in rations for growing pigs. 4. Effects of sunflower oil and coconut oil on protein and fat retention, fatty acid pattern of back fat and blood parameters in piglets

Rations containing 12% sunflower oil (Ration II) and 12% coconut fat (Ration III) were compared with a control ration (Ration I) in a 34 day experiment with growing boars of the German Landrace breed (12-30 kg body weight). The relationships between DP and ME were held constant for all 3 rations, and because of the higher ME contents of the two fat rations, this was achieved by reducing the feed intake, relative to that of the control ration. Parameters measured were growth, composition at slaughter, the apparent digestibility of the crude nutrients and energy, the N-balance and the concentrations of urea, insulin, glucose, triglyceride and cholesterol in the blood. In comparison to Ration I, the apparent digestibilities of crude protein in Rations II and III were 5 and 4% (p less than 0,05) higher, respectively. There was little difference in the apparent digestibility of crude fat between the Rations II and III. However, large differences in the values were determined depending upon method of extraction. There were little differences in the productive performance of the animals fed the fat diets. The control animals had, however, a 13% lower growth rate (p less than 0,05) when compared at similar ME-intakes. As the energy concentration and the growth rate were higher in groups II and III, the feed conversion efficiency and the ME required per kg growth were approximately 30 and 13% lower than that of the control animals. The efficiency of protein utilization of the animals in group III was 4% higher (p greater than 0.05) and the blood urea concentration 20% lower (p less than 0.05) than that in group II. The values for the control animals were intermediate. A similar result was obtained concerning the fat content of the animals. The fat content of the animals in group III was 15.9% and this was significantly lower (p less than 0.001) than that of 21.1% measured in group II. That of the control animals, 18.6%, was not significantly different from the above values. The differences in feeding over the relatively short period of 34 days lead to marked differences in the fatty acid pattern of the backfat. The contents of myristic acid and linoleic acid were significantly different between group II and III; for the former values of 0.8% and 16.9% were determined, respectively, with corresponding values of 48.7 and 11.3% for the latter.(ABSTRACT TRUNCATED AT 400 WORDS)     

Urea utilization of growing lambs. 2. Growth experiments

In two growth experiments with 30 lambs per group the influence of urea (1-2% of the ration) and straw (20-30% of the ration) on the performance was studied under conditions of intensive fattening. The content of native crude protein in the rations varied between 10.1 and 18.4% of the DM. In experiment 1 the lambs of the two groups which received mixed feed for fattening lambs without urea on average consumed with 1.02 and 1.11 kg DM resp., 696 and 757 EFUcattle resp. and 173 and 189 g crude protein resp. per animal and day. The groups with wheat or barley and urea consumed 1.06 and 0.96 kg DM resp., 714 and 627 EFUcattle resp. and 209 and 155 g crude protein resp. Their weight gain of 247 g/animal and day was 24% and that of 230 g resp. 26% higher than that in the control groups without urea. The lowest dry matter intake (0.91 and 0.82 kg resp.) was shown by the animals of the groups which received wheat or barley without urea. In the second experiment the control group achieved an average daily weight gain of 327 g at an expenditure of 2.24 kEFUcattle/kg weight gain. Despite a partly higher dry matter intake, the daily EFUcattle intake was between 12.2 and 24.5% lower in the straw groups and energy expenditure increased between 12.0 and 27.8%. Urea supplements of between 1 and 2% improved dry matter, EFUcattle and crude protein intake and thus weight gain.     

Effects of rumen-protected methionine in a low protein ration on metabolic traits and performance of early lactating cows as opposed to rations with elevated crude protein content

A 5‐week experiment with 24 multiparous early lactating Brown Swiss cows was conducted to investigate the effects of supplementary rumen‐protected methionine in conjunction with dietary protein reduction on metabolism and performance after 1 week of control measurement. Three rations containing 175, 150 and 125 g of crude protein/kg feed dry matter were supplemented with methionine. The fourth ration, also only containing 125 g of crude protein/kg dry matter, remained unsupplemented. The four treatment groups had a similar metabolic supply of other essential amino acids, protein and energy, as calculated by various approaches. The two low protein rations were, however, slightly deficient in ruminally degraded protein. Treatment effects remained low on feed intake, forage meal pattern, milk yield and fat as well as lactose content. In contrast, the content and yield of milk protein significantly declined only in the unsupplemented low protein ration relative to the initial value. Compared with this ration, the decline in milk protein yield was clearly delayed in the supplemented low protein ration. Blood plasma methionine tended to be reduced without supplementation and to be increased with additional methionine. Supplementation of methionine reduced other plasma amino acids. Plasma insulin, glucose, lactate, ketone bodies and aspartate amino transferase activity indicated a certain liver stress and a somewhat elevated energy requirement with high and particularly with low protein content (when unsupplemented). Methionine improved metabolic protein utilization, followed by the lowest plasma, urine and milk urea levels in the supplemented low protein diet. In conclusion, no major adverse effects were assessed under the conditions tested. Supplementation of methionine may nevertheless be useful in rations with particularly low protein content fed to early lactating cows in order to prevent negative long‐term effects which were only visible here as trends.     

The energy metabolism of growing swine in the liveweight range of 10-50 kg. I. Study design, feed intake and digestibility

Studies of the energy metabolism at maintenance and growth levels after the feeding of rations with a crude protein content of 17-24% and 44-47% resp. were carried out with hybrid pigs of line 150 in the live weight range between 10 and approximately 50 kg. This paper gives information on the methods and the outlay of the experiment and presents results concerning feed intake, live weight development and digestibility. Feed intake increased on average with growing live weight by 30-35 g DM/kg live weight. Feed conversion ranged from 1.2 to 1.8 kg DM/kg live weight gain in the first period and from 2.3 to 3.2 kg DM/kg live weight gain in the last period. The digestibility of the energy in the rations with a crude protein content of between 17 and 24% averaged 80% and that of the rations with a crude protein content of 44-47% averaged 86%. In the course of ontogenetic development the digestibility increased up to about 30 kg LW. The influence of the nutritional level on the level of digestibility was unequal in the experiments. In one experiment a decrease (1% unit) and in two experiments an increase (1-3% units) of the digestibility after the feeding of growth level in contrast to maintenance level could be observed. The change of rations with a varying protein content did not result in an influence on the digestibility level in comparison with the constant feeding of one ration.     

Studies on nitrogen metabolism in the large intestine of ruminants. 5. Metabolism of intra-cecally infused 15N-urea without and with fermentable material in heifers

Six heifers with a live weight of 215, 227 and 238 kg (experiment 1) and 220, 227 and 233 kg, resp. (experiment 2), were supplied with ileocaecal re-entrance cannulae, jugular venous catheters and bladder catheters. The ration consisted of 4 kg maize silage and 4 kg wheat straw pellets per animal per day. Up to 3.5 kg of the straw pellets, consisting of 73% wheat straw, 10% barley, 12% molasses, NPN salts and a mineral mixture, were consumed per animal per day. In a preliminary period 50% of the digesta flow was collected over 12 h/d on 5 consecutive days and stored in a deep-freeze. During the main trial the re-entrance cannula was disrupted and the flowing digesta were quantitatively collected at the end of the ileum; previously collected digesta were supplemented with 15N urea and every hour over 24 h infused into the caecal part of the re-entrance cannula. Between the 24th and 30th hours the digesta were infused without 15N urea supplement. In trial 2 the digesta were also supplemented with partly hydrolysed straw meal between the 1st and 30th hours (approximately 10% straw meal DM related to digesta DM). There were no differences between trials 1 and 2 with regard to the increase of atom-% 15N excess (15N') in the plasma urea. The 15N labelling decrease of the plasma urea N shows that the half-life is 7.9 h in trial 1 and 7.0 h in trial 2. The NH3 nitrogen in faeces was distinctly higher labelled in trial 2 after the supplement of straw meal than in trial 1. The total N in faeces was also twice as highly labelled as in trial 1. Atom-% 15N' in urine was significantly higher in trial 2 than in trial 1 between the 6th and 16th hours after the beginning of 15N urea supplementation. In the decrease curve of atom-% 15N' (after the 26th hour of trial) the values in trial 1 were generally higher than in trial 2. The higher bacterial protein synthesis in the large intestine in trial 2 (after the supplement of partly hydrolysed straw meal) had the effect that 13.6% of the supplemented 15N' was excreted in faeces by the 30th hour of trial, in contrast to this only 4.7% in group 1. Up to the 4th day after the 15N urea infusion these values increased to 16.2 and 6.1%, resp., only.     

Evaluation of 15N marked urea in the laying hen. 4. Incorporation of 15N in blood, its fractions and follicles in various developmental stages

In order to study the utilization of urea in poultry, 3 colostomized laying hybrids were orally supplied with a traditional ration supplemented with 1% 15N'-labelled urea with a 15N excess (15N') of 96.06 atom-% over a period of 6 days. After another 2 days on which the hens received the same ration with unlabelled urea, they were butchered. The atom-% 15N' of the blood on an average of the 3 hens was 0.64, of the plasma 1.40 and of the corpuscles 0.47. The TCA-soluble fraction of the blood had an average 15N' of 1.14 atom-%; the 15N amount is 9.7% of the total amount of 15N in the blood. The amount of 15N' in the urea in the blood was 6.8 atom-%. This shows that the absorbed urea is decomposed very slowly. The quota of 15N' in the basic amino acids from the total 15N' of the blood plasma is only 0.3% and that of the corpuscles 2.2%. The average 15N' of the mature follicles is 2.39 atom-% whereas the smallest and the remaining ovary contain 1.12 atom-%. The labelling level of lysine in mature egg cells was, in contrast to this, only 0.08 atom-% 15N' and in infantile follicles 0.04 atom-% 15N'. 1% of the 15N' quota is in the follicles and the remaining ovary. Of the basic amino acids, histidine is most strongly labelled. The as a whole lower incorporation of the 15N from urea into the basic amino acids shows that the nitrogen of this compound can be used for the synthesis of the essential amino acids to a low degree only.