European reference method for the in vivo determination of metabolisable energy with adult cockerels: reproducibility, effect of food intake and comparison with individual laboratory methods

1. A common reference procedure adopted by several European laboratories to determine apparent metabolisable energy corrected to zero-nitrogen balance (AMEn) is described. 2. Reproducibility has been estimated by comparing results from 4 diets measured in 7 laboratories. The standard deviations between laboratories of dry matter, gross energy, Kjeldahl nitrogen and AMEn were respectively, on average, 11.29 g/kg, 0.242 MJ/kg, 1.56 g/kg and 0.380 MJ/kg dry matter; the corresponding coefficients of variation between laboratories were 1.27, 1.29, 4.39 and 2.92%. 3. Effect of food intake was tested by comparing AMEn from birds fed either 0.90 or 0.45 of ad libitum: the amount of food intake had a negligible effect on AMEn values. Endogenous energy losses corrected (EELn) or not (EEL) to zero nitrogen balance were estimated either by regression between excreted energy and ingested energy or in fasted and glucose-fed cockerels. EELn estimated by regression was, on average, 8.7 kJ/bird/d.; it was independent of diet composition. EEL and EELn determined in fasted or glucose-fed birds were higher than those determined by regression. 4. AMEn values measured by individual laboratory procedures were very close to those obtained by the reference method, except from laboratories using a tube feeding procedure, where deviations were probably a consequence of overestimated EEL.     

Comparison of metabolisable energy values of different foodstuffs determined in ostriches and poultry

Apparent (AMEn) and true (TMEn) metabolisable energy values, corrected for nitrogen retention, of wheat bran, saltbush (Atriplex nummularia), common reed (Phragmites australis), lupins, soyabean oil cake meal (SBOCM), sunflower oil cake meal (SFOCM) and fishmeal were compared in 7 successive trials using 12 mature South African Black ostriches and 10 adult Australorp cockerels per ingredient. TMEn values of 11.91, 7.09, 8.67, 14.61, 13.44, 10.79 and 15.13 MJ/kg for wheat bran, saltbush, common reed, lupins, SBOCM, SFOCM and fishmeal, respectively, were found for ostriches in comparison to lower (P<0.05) values of 8.55, 4.50, 2.79, 9.40, 9.04, 8.89 and 13.95 MJ/kg for cockerels. The higher (P<0.05) ME values for ostriches confirm that the ostrich is capable of digesting foodstuffs, especially those with high fibre concentrations such as drought-resistant fodders, more effectively than poultry. Plant protein sources could make a considerable energy contribution to diets for ostriches. It is concluded that it is essential to use energy values of foodstuffs determined using ostriches and not extrapolated values derived from poultry in diet formulation for ostriches.     

Effects of sex,age and food intake upon metabolisable energy values in broiler chickens

1. Nitrogen‐corrected apparent metabolisable energy (AME_n) values of 2 diets with different energy: protein ratio were estimated in an experiment with 8 groups of female and 8 of male chickens in 15 sequential 3‐day balance periods from the 12th to the 56th d of age.

2. The effect of sex on AME_n values was not significant.

3. The effect of age was highly significant. AME_n values of the mixture with the narrower energy: protein ratio increased with age. The dependence of AME_n of the diet with the wider energy: protein ratio on age was parabolic, AME_n values increasing only until the 37th day of life.

4. Under conditions of ad libitum feeding, AME_n of the mixture with the wider energy: protein ratio given to female chickens decreased significantly with increasing food intake.     

Effect of feeding technique, ad libitum, dry or wet force feeding, on the metabolisable energy values of raw materials for poultry

1. Metabolisable energy values (AME, AMEn, TME and TMEn) of three raw materials (maize, sunflower meal and soyabean meal) were determined in adult cockerels using two classical feeding e techniques (ad libitum and force-feeding of dry food) and a new one in which birds were force-fed wet diets. 2. In the wet force-feeding assay nitrogen balances and food intakes were similar to those achieved with ad libitum feeding. The duration of the assay using wet force-feeding was only 2 d as compared to the 3 or 7 d experimental periods for the dry or the ad libitum assays respectively. 3. TMEn values were not dependent on the feeding technique used; AME and AMEn data obtained in the ad libitum and wet force-feeding assays were close to TMEn values. As expected, these values were underestimated in the dry force-feeding assay.     

True metabolisable energy, heat increment and net energy values of two high fibre foodstuffs in cockerels

1. The yields of true metabolisable energy (TME) and net energy (NE) from chaya leaf meal and wheatfeed were mcasured in tube-fed cockerels. 2. TME, 5.76 MJ/kg, from chava leaf meal was lower than from wheatfeed, 8.39 MJ/kg. The total heat increment attributable to the feeding of chaya leaf meal was 1-7 times greater than that of wheatfeed. 3. The net efficiency of utilisation of ME (k) from chaya leaf meal was 0.64, while that from wheatfeed was 0.86. The role of different chemical composition, especially the high fibre content of the materials, is discussed. 4. The metabolisable energy and net energy values derived from chava leaf meal represented 0.34 and 0.23 respectively of its gross energy content. The combination of lower TME and lower net efficiency of utilisation led to chaya having a NE value, 3.86 MJ/kg, which was only 0.53 that of wheatfeed.     

The effects of age,dietary fat and bile salts,and feeding rate on apparent and true metabolisable energy values in chickens

1. Apparent (AME) and true (TME) metabolisable energy values of four diets, containing 50 or 150 g animal fat or maize oil/kg, were estimated in young and adult chickens. The diets were given with and without a supplement of 5 g bile salts/kg. Three feeding rates, ad libitum, and l/6th or 1/3rd of ad libitum were compared.

2. In younger birds, endogenous energy losses were higher when measured in starved birds than when estimated by regression analysis.

3. In young birds, feeding rate had no effect on AME of diets containing 50 g lipids/kg but it significantly affected TME. These results were reversed in adults. AME and TME values of diets containing 150 g lipids/kg were affected by the feeding rate in both young and adult birds.

4. Bile salts increased metabolisable energy values of diets containing high concentrations of saturated fatty acids and their effect was more pronounced in young birds.     

A note on the effect of temperature on true and apparent metabolisable energy values of a layer diet

The effect of ambient temperature on the true (TME) and apparent metabolisable energy (AME) values of a layer diet was examined using White Leghorn cockerels.

The TME value found at the cool temperature (5 to 15 °C) was significantly higher than those found at hot (25 to 35 °G) and control (22 °C) temperatures. AME values were not significantly affected.     

Metabolisable energy studies with Turkeys: Nitrogen correction factor in metabolisable energy determinations

1. Metabolisable energy (ME) values, uncorrected for nitrogen retention, for a Canadian rapeseed meal and an American wheat, determined by a regression method with turkey poults, were influenced by the protein content of the basal diet used.

2. Increased nitrogen retention offsets the effect of substituting rape‐seed meal into a low‐protein basal diet, providing a high estimate of ME.

3. The expected offsetting due to nitrogen retention of the effect of substituting wheat into a high‐protein basal diet was not observed but this was due to some unexpected trends in nitrogen retention.

4. Correction of ME values for nitrogen retention decreased differences due to disparities between the protein contents of the ingredients evaluated and the basal diet.     

Comparison of two direct bioassays using 3-week-old broilers to measure the metabolisable energy of diets containing cereals high in fibre: differences between true and apparent metabolisable energy values

1. Nitrogen-corrected apparent and true metabolisable energy contents (AMEN and TMEN) of 12 diets, containing different amounts of maize, wheat, barley and rye, barley with beta-glucanase and maize with 0.05 g/kg guar gum were measured using 3-week-old male broilers. 2. The AMEN method involved: 4 d of dietary adaptation, 24 h of starvation, 54 h of ad libitum feeding, 24 h of starvation and daily total droppings collection. TMEN was measured after a 48 h starvation period followed by 2 d of tube-feeding two doses of 15 g of the diets and quantitatively collecting all the droppings after 48 h of starvation. The endogenous energy losses (EELN) were measured after tube-feeding 8 chickens with 30 g of glucose, also over 2 d. 3. The results show that a significant interaction exists between the nature of the diets and the method used to measure metabolisable energy. Differences between TMEN and AMEN values ranged from 1.03 to 1.98 MJ/kg dry matter. These differences were positively correlated with the total pentosan contents of the diet (r = 0.94), the natural logarithm of the viscosities of the water extracts (r = 0.87), the sum of the contents of total pentosans and total beta-glucan (r = 0.85), the calculated total non-starch polysaccharide contents (r = 0.79), the neutral detergent fibre contents (r = 0.76) and the total beta-glucan contents (r = 0.70). Furthermore, a significant interaction was found between diets and the method used to derive lipid digestibility. The differences between apparent and true lipid digestibility ranged from 0.05 percentage points for the wheat diet to 0.20 percentage points for the rye diet. 4. From the results of this trial, it appears that TMEN overestimates the energy value of high fibre diets.     

Endogenous losses of energy and amino acids in birds and their effect on true metabolisable energy values and availability of amino acids in maize

1. Endogenous losses of amino acids (EAAL) and energy (EEL) were determined in unfed adult cockerels. The intercepts of linear regression analysis were determined using 44 birds precision-fed on maize. During the experimental period (48 h), excreta of birds were collected, and the samples of maize and the excreta were dried, ground and assayed for gross energy and amino acids. 2. The EAAL and EEL in unfed cockerels influenced true available amino acid (TAAA) values. Therefore, the intercept of regressions showed an increase in TAAA values of maize. 3. The results indicated that there was no significant difference between the data obtained for EEL from the unfed birds and from regression analysis so, the figure from regression analysis could be used for calculating the true metabolisable energy (TME) value of maize. 4. The calculated EAAL from regression analysis caused an increase in the TAAA value in maize. The amounts of metabolic and endogenous amino acid excretions varied in voided excreta from unfed birds. These differences would be related to genetics, age, sex and environmental temperatures.     

A comparison of a new net energy system with the metabolisable energy system in broiler diet formulation,performance and profitability 1

Two trials were conducted with unsexed broilers to compare a net energy (NE) system and a metabolisable energy (ME) system on least‐cost broiler diet formulation, broiler performance and economic efficiency. Both energy systems were compared in the range of 3000 (2161) to 3400 kcal ME/kg (2560 kcal NE/kg) using rations with increasing energy concentration of about 100 kcal/kg food.

The two different energetic evaluation systems had considerable effect on dietary composition, the penalty cost of rejected ingredients, the marginal profit of some limiting constraints and the position of the least‐cost nutrient concentration. The starter and finisher rations, based on NE values, were on average 4.77 and 2.43 BF²/100 kg cheaper, respectively than those based on ME values. For equal NE contents, they contained 50 to 70 kcal less ME/kg and 1% less crude protein.

The broiler performances were on average better on the NE‐diets. The mean difference of 20 to 30 g in body weight was significant at 4 and 6 weeks (P < 0.01 and P < 0.05).

Regression analysis indicated no significant effect of rising energy concentration on food intake with the ME‐diets, but a significant (P < 0.05) linear decrease with the NE‐diets of 1.16 ± 0.34 and 1.72 ± 0.37 g/chick d at 6 and 8 weeks respectively for every 100 kcal/kg rise in the NE content of the ration. As a result body weight at 6 weeks improved linearly per increment of 100 kcal NE/kg with 37.2 ± 3.2 g (P < 0.05) on the ME‐diets and with 18.8 ± 6.8 g (P = 0.08) on the NE‐diets.

The efficiency of food utilisation, although slightly better on the NE‐diets, was not significantly affected by the energy systems. As expected, linear improvements (P < 0.001) of respectively 58 ± 6 and 62 ± 11 g food/kg weight gain at 6 and 8 weeks were noted for every increment of 100 kcal NE/kg diet.

Returns over food costs were for the whole energy range higher on the NE‐diets (average 0.66 BF/chick, variation 1.01 to 0.23 BF/chick). Gross profit increased with rising nutrient density from 16.33 to 17.97 BF/chick on the ME‐diets and from 17.34 to 18.23 BF/chick on the NE‐diets. The data illustrate that the economical efficiency of broiler production can be considerably improved by taking into account the effect of both energy content and energy system.     

Interactions between fats of differing chemical content: apparent metabolisable energy values and apparent fat availability

1. Tallow (A) and rape oil (E) were obtained for evaluation. They were blended in the ratios A95:E5, A90:E10 and A80:E20. The three blends together with the two pure fats were each included at 40, 80 and 120 g/kg into a basal diet. 2. The experimental diets were evaluated for apparent metabolisable energy corrected to zero nitrogen retention (AMEN MJ/kg) and apparent fat availability (g/kg) using 6 replicates of a cage of two male broiler chicks 14 d old and 8 replicates of a cage of one Rhode Island cross cockerel approximately 1 year old. Diets were fed for 72 h then removed for 24 h. This was followed by a 48 h period when food was available ad libitum and a further 24 h of starvation. A total collection of excreta was undertaken each 24 h for the latter 72 h period. 3. Evaluation of AMEN and apparent fat availability for the individual fat blends was achieved through both linear and quadratic regression. 4. Synergism, as demonstrated by a higher determined than calculated AMEN value, was detected with fat blends fed to chicks but not cockerels and only at rates of inclusion beyond 80 g/kg. 5. No consistent differences between AMEN determined through calorimetry or AME determined with reference to apparent fat availability multiplied by fat gross energy were detected.     

Electroneurographic examination of the ulnar and radial nerves in the dog: reference values, biological variation and reproducibility

The radial and ulnar nerves were examined electrophysiologically in 90 normal dogs. In 66 of these dogs, aged between one and eight years, the reference values were established for 27 variables. Multicomponent sensory nerve action potentials were encountered at the proximal recording site in the ulnar nerve in 68 per cent of the dogs in the reference group and in the radial nerve in 26 per cent. Differences between the sexes were not significant, nor were differences between two breeds of similar body size. There were no significant age related differences between the ages of one and eight years. Limb length, measured as the distance between sensory stimulation site (digits) and proximal recording site (elbow), was found to have a significant effect on the velocity, amplitude, number of positive peaks and duration of the nerve action potentials. The variation in results of repeated measurements of velocities ranged from 0 to 11 per cent. The relative error in velocities due to errors in measurement of distance and latency ranged from 1 to 12 per cent.     

家禽饲料有效能值的测定及影响因素

<正>客观准确地评定饲料原料和饲料的有效能值是开发利用饲料资源及优化饲料配方的主要决策依据。实践中,为了经济地配制家禽日粮,就要准确地测定各种饲料原料中(尤其是能量饲料)的有效能值,低估了能值,就会在最低成本日粮中拒用一种成分,但     

Comparative apparent metabolisable energy values of high, medium and low tannin varieties of sorghum in cockerel, guinea fowl and quail

1. Nitrogen-corrected apparent metabolisable energy values (AMEN) of three varieties of sorghum (white-low tannin, brown-medium tannin and red-high tannin) were measured in three species of poultry (cockerel, guinea fowl and Japanese quail) by a practical diet replacement (total collection) method. 2. Each variety of sorghum was tested at two concentrations (200 and 400 g/kg of reference diet) in 6 replications with one cockerel or guinea fowl or two quails per replication. The duration of the trial included a 10 d preliminary feeding period (on conventional grower diet) followed by a 12 d adaptation period (on reference and test diets) and a 3 d balance period (with recording of feed intake and excreta output). 3. The calculated AMEN values of different sorghum varieties were: white--12.9, 12.8 and 12.7; brown--12.7, 12.3 and 12.6; and red--11.4, 11.1 and 11.6 MJ/kg for cockerels, guinea fowls and quails, respectively. The mean AMEN value of red sorghum (11.3 MJ/kg) was significantly lower than those of brown (12.5 MJ/kg) or white sorghum (12.8 MJ/kg). A negative correlation was observed between tannin concentration and AMEN. 4. There was no significant difference in the AMEN values of white, brown and red sorghum varieties to the different poultry species. AMEN values of sorghum for the cockerel could, therefore, be used in practical feed formulation for guinea fowl and quail.     

Influence of substitution method and of food intake on bioassays to determine metabolisable energy with chickens

1. Several different methods of assaying the metabolisable energy (ME) of ground maize and a maize and glucose mixture were studied. Over a 24‐h period fasted cockerels lost more energy and nitrogen in their excreta than those fed 15 g maize and 15 g glucose monohydrate.

2. Discrepancies in ME values of maize were found between 1) Hill's method (substitution for glucose) and 2) Sibbald's method (the difference between energy ingested and excreted, corrected for endogenous losses by a comparison with fasted controls). These discrepancies were attributed to differences in endogenous energy losses between fed and fasted birds and interactions between the test substance and reference diet.

3. No significant differences could be detected when substitution for glucose was compared to substitution for the entire diet in three experiments.

4. Significant differences in the ME of maize because of the composition of the basal diet were found (semi‐purified: practical; 17·20:14·56 kJ/g; and 50 g/kg added fat: 100 g/kg added fat; 15·94:16·69 kJ/g).

5. Food intakes equal to 70, 60 or 30% of ad libitum did not affect the ME of maize when the substitution for glucose method was used.

6. It is concluded that basal diets for ME determinations should be carefully selected because of possible interactions between dietary components. When ME is determined by feeding small amounts of the test material, endogenous losses may be over‐estimated because the control birds are in a different physiological state (fasted).

     

Effect of age on reference intervals of serum biochemical values in kittens

OBJECTIVE: To determine the effect of age on reference intervals of serum biochemical values in kittens. DESIGN: Prospective clinical trial. ANIMALS: 55 kittens from 12 specific-pathogen-free queens. PROCEDURE: Kittens were allocated at birth into colostrum-fed (n = 27) and colostrum-deprived (28) groups. Blood was collected at birth and on days 1, 2, 4, 7, 14, 28, and 56. Serum samples were analyzed for activities of alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, creatine kinase, lactate dehydrogenase, gamma-glutamyltransferase, amylase, and lipase and for concentrations of albumin, total protein, bilirubin, urea nitrogen, creatinine, cholesterol, glucose, calcium, phosphorus, and triglycerides by use of an automated analyzer. Total serum solids concentrations were determined by use of refractometry. Serum IgG concentrations were quantified by use of radial immunodiffusion. RESULTS: For several analytes, reference intervals changed rapidly, most notably during the first few days of life. Reference intervals for alkaline phosphatase, creatine kinase, lactate dehydrogenase, and triglycerides were higher from birth to 8 weeks than adult reference intervals. Aspartate aminotransferase, bilirubin, urea nitrogen, and creatinine were higher than in adults at birth but were similar to or lower than adult reference intervals by 8 weeks. Compared with adult reference intervals, reference intervals for calcium and phosphorus concentrations were higher and for albumin and total protein concentrations were lower throughout the study period. CONCLUSIONS AND CLINICAL RELEVANCE: Important differences exist between reference intervals for serum biochemical values of neonatal and adult cats. Age-appropriate reference intervals should be used for accurate assessment of serum biochemical test results in cats.     

The estimation of endogenous excreta and the measurement of metabolisable energy in poultry feedstuffs using four feeding systems,four assay methods and four diets

1. Four different methods (dual semi‐quick (DSQ), conventional, a true metabolisable energy (ATM) method and Farrell's rapid method) were used to measure in adult roosters the apparent metabolisable energy (AME) and true metabolisable energy (TME) of four maize‐based diets with bran inclusions of 0, 200, 400 and 600 g/kg

2. Daily food intakes per bird were 75 g (or ad libitum) (H), 35 g (M) and 10 g (L). AME values determined by DSQ, conventional and Farrell methods were not different at the two highest intakes but were depressed at L intakes. ATM method often gave different values from other methods, particularly at the lowest intake.

3. The linear relationships between food intake and excreta energy yielded intercept values of 13 to 32 kJ/d for three methods; but ATM method yielded intercepts of 31 to 52 kJ/d. In a separate experiment it was demonstrated that a linear model may not be the most appropriate fit to such data. Removal of data for the 10 g/d intake yielded linear regression equations with intercepts not significantly different from zero for the two continuous feeding methods (i.e. a zero estimate for endogenous urinary and metabolic faecal energy (EEL), but for the two methods using a single input after fasting, intercepts were almost always positive. This confirms Härtel's (1986) observation of the absence of EEL under continuous feeding but its ever presence using a TME assay.

4. Correction of AME for EEL to obtain TME tended to increase values for all diets and also within a diet with decreasing intakes. The effect of correcting AME to nitrogen balance (n) was to give AME_n values that were more consistent between diets and reduced differences between methods. For the conventional method differences between the three intakes on all diets were greatly reduced.

5. There is reason to be concerned about the many different metabol‐isable energy values obtained using the ATM method compared to the three other methods and the basis for correcting for endogenous excreta. It is concluded that because of the uncertainty of EEL values, their variation and application, the AME system should be retained.