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A study was performed to investigate the effect of environmental temperature (16 degrees C, 24 degrees C or 32 degrees C) and dietary fiber (DF) on energy expenditure and quantitative oxidation of nutrients in rats. Forty-eight male rats, initial body weight 90-105 g, were allocated to eight groups in two series. The rats kept at 24 degrees C was repeated in both series. Low and high fiber diets (56 vs. 257 g DF/kg dry matter) were studied in 6-week balance experiments. The rats in all groups were offered the same amount of air-dried food. Indirect calorimetry was used to measure the energy metabolism. The difference in heat production (HP) calculated by RQ and CN methods was < 2% and was not affected by environmental temperature and DF. The relation between fat and protein oxidation changed from 1.54 to 1.00 when the ambient temperature changed from 16 degrees C to 32 degrees C. The contribution of carbohydrate oxidation to total HP was lowest at 16 degrees C, whereas the fat and protein oxidation was highest at 16 degrees C. The oxidation of nutrients was not influenced by DF. The additional energy retained at the higher temperatures had a constant ratio between fat and protein, i.e., 70:30. At an energy retention of 65.8 kJ/kg0.75 d or less, body fat is mobilized and only protein deposited. Because of higher HP, rats living in the cold environment used more fat as substrate for HP than rats kept in warmer environments. The cold environment results in an increase in the amount of interscapular brown adipose tissue, but no significant difference was found between DF levels.

Energy values of non-starch polysaccharides (NSP) were estimated from NSP fermentability and from digestible energy balances in human subjects and in rats. During four studies, humans consumed four low fiber control diets and six high fiber diets. For the rat diets, duplicates of the foods consumed by humans were mixed together, freeze-dried and ground. Calculated from fermentability, partial digestible energy values of NSP in humans and rats, respectively, were 8.2 +/- 1.3 and 5.7 +/- 1.2 (P = 0.0013, fruits and vegetables), 11.4 +/- 0.7 and 5.7 +/- 3.2 (P = 0.0001, citrus fiber), 5.0 +/- 2.1 and 2.2 +/- 3.3 (P = 0.0429, barley fiber at high protein intake), 4.4 +/- 1.8 and 2.4 +/- 2.0 (P = 0.0561, barley fiber at low protein intake), 6.7 +/- 1.4 and 7.6 +/- 1.2 (P = 0.296, coarse whole meal rye bread), and 7.1 +/- 0.6 and 6.1 +/- 1.7 (P = 0.157, fine whole meal rye bread) kJ/g NSP. Calculated from energy balances, partial digestible energy values of NSP in humans and rats, respectively, were 2.1 +/- 3.5 and -5.0 +/- 4.0 (P = 0.026, fruits and vegetables), 10.7 +/- 5.1 and 1.4 +/- 5.6 (P = 0.003, citrus fiber), 1.6 +/- 5.1 and -17.8 +/- 8.6 (P = 0.0001, barley fiber at high protein intake), -2.6 +/- 4.9 and -9.3 +/- 8.2 (P = 0.044, barley fiber at low protein intake), -3.0 +/- 7.0 and 0.9 +/- 2.5 (P = 0.27, coarse whole meal rye bread), and 0.9 +/- 5.1 and 0.6 +/- 3.7 (P = 0.89, fine whole meal rye bread) kJ/g NSP. Net energy values were 70% of digestible energy values. Differences between species were significant for NSP in fruits and vegetables, citrus fiber, and barley fiber at high protein intake. Most energy values calculated from energy balances were significantly lower than values calculated from NSP fermentation, with differences being greater in rats than in humans. Thus, the energy values of some types of NSP contained in mixed diets could not be estimated accurately from NSP fermentability either in humans or rats. In addition, our results suggest that the rat is not always a suitable model of humans for predicting energy values of NSP in mixed diets.

The hypothesis was tested that fermentable dietary fibre (DF) sources elevate faecal N excretion at the expense of urinary N without affecting N retention. DF that substantially increase fermentation (pectin, sugarbeet and soya bran) or are poorly fermented (crystalline cellulose and maize bran) were fed as supplements to a basal DF-free diet at three dose levels: 0, 50 and 100 g supplement/kg basal diet. The diets were fed to juvenile male Wistar rats for 2 weeks before a 7 d period when faeces and urine were collected. Faecal excretion of N was significantly increased, dose-dependently, by all DF supplements and was positively correlated to faecal bulking. Urinary excretion of N was lower at the high doses of the DF supplements but reached significance only with the highly fermentable (0.68) sugarbeet-supplemented diets. Regression analysis showed that the major part (0.75) of the increase in faecal N excretion due to DF supplementation was balanced by a reduction in urinary excretion; N retention was therefore, at the dose levels used, only affected to a small extent. Only in the maize-bran-supplemented diets were the reductions in N retention significant. The shift in N excretion from urine to faeces can be explained largely by the degree of microbial fermentation in the large intestine caused by the addition of DF supplements and emphasizes the modifying role that certain DF supplements may have on the enterohepatic cycle of N. Possible implications of these findings for patients with liver or renal failure or for conditions when the intake of dietary protein is marginal are discussed.

The present study was undertaken to provide detailed information about the effect of dietary fibre (DF) level on the development of the digestive tract, on nutrient digestibility and on energy and protein metabolism of pigs housed in low (13 degrees) or high (23 degrees) thermal environments. Low- and high-fibre diets (59 v. 268 g DF/kg DM) were studied in three balance periods with fistulated pigs in the weight range 45-120 kg. Heat production was measured using open-circuit respiration chambers. Pea fibre and pectin were used to adjust the DF level in the high-fibre diet. Per kg empty body weight the stomach, caecum and colon and the length of colon were significantly greater in pigs consuming the high-fibre diet than in those on the low-fibre diet. Pigs kept at low temperature had significantly heavier caecums than those kept at the high temperature. Digestibilities of protein, DM and energy were lowest for the high-fibre diet. Only minor amounts of NSP and its constituent sugars were degraded anterior to the ileum, whereas in the hind-gut the fermentation of the total NSP fraction was high, being 0.77 for the high-fibre diet and 0.59 for the low-fibre diet. Feeding the high-fibre diet increased the flow of digesta through the terminal ileum 5-6-fold and an extra 460 g organic matter was fermented daily in the hind-gut compared with pigs fed on the low-fibre diet. The amount of retained energy as a proportion of metabolizable energy decreased in relation to the amount of energy fermented in the hind-gut. Based on the present data it was estimated that the relative value of energy derived from hind-gut fermentation was 0.73 in comparison with energy enzymically digested in the small intestine. There was negligible effect of the temperature--fibre interaction on energy metabolism. However, it could be calculated that the decrease in temperature from 23 degrees to 13 degrees was associated with an increase in heat production by 2.9 MJ/pig per d.

The present study was undertaken to provide detailed information about the effect of fibre source (pea fibre, wheat bran or oat bran) at inclusion levels of 0, 187 and 375 g/kg diet on the development of the digestive tract, nutrient digestibility and energy and protein metabolism in broiler chickens. Heat production was measured using open-air-circuit respiration chambers. Diets with increasing levels of pea fibre decreased the DM in droppings and increased excreta output (2.5-fold) relative to DM intake. Adaptation to increased dietary fibre levels included increases in the size of the digestive system, with pea fibre exerting a stronger impact than wheat bran or oat bran. The length of the intestine, and particularly the length and weight of the caecum, increased with the fibre level. The digestibility of all nutrients also decreased with increasing fibre level. The decrease in the digestibility in relation to NSP for the three fibre sources was bigger for oat bran (0.0020 per g dietary NSP) than for pea fibre and wheat bran (0.0014 and 0.0016 per g dietary NSP) indicating that the cell walls in oat bran (aleurone and subaleurone) had a significant negative effect on the digestibility of cellular nutrients, i.e. protein and fat. The degradation of the NSP constituents was far lower in chickens than found in other animal species such as pigs and rats, thus supporting the view that chickens do not ferment fibre polymers to a great extent. Excretion of organic acids (mainly lactic acid and acetic acid) accounted for up to 2% of metabolizable energy (ME) intake with the highest excretion for the high-fibre diets. H2 excretion was related to the amount of NSP degraded and indicated higher microbial fermentation with increasing fibre levels. The chickens' feed intake responded to a great extent to dietary ME concentration but expressed in terms of metabolic body size (W0.75) ME intake was depressed at the high fibre levels. Dietary NSP was able to explain between 86% (oat bran) and 96% (pea fibre) of the variation in ME concentration. The amount of energy available from fermentation of NSP appears to reach a maximum of 42 kJ/d independent of fibre source and level. Expressed in relation to ME intake the NSP fermentation contributed 3-4%. With increasing fibre intake the partitioning of retained energy between body protein and body fat changed in favour of protein.

In pot experiments with greatly differing rates of N, P, S, K and Ca, dry matter (DM) yields of leek stems varied from 25 to 164 g/pot. Total-N and NO3-N concentrations varied from 1.18 to 3.56% and from 10 to 1515 ppm in DM, respectively. Both N applications and P and K deficiency greatly increased total-N and NO3-N content. S applications increased total-S content from 0.047 to 0.359% in DM, of which between approximately 100 to 25% were found in methionine+cystine. Total-N/total-S ratios decreased from 57 to 6 with the highest S level. P and K applications increased their respective content in DM two- and threefold. Severe Ca deficiency reduced Ca content from 0.495 to 0.045%. Iron, zinc, manganese and copper contents varied from 33-69, 14-26, 11-34 and 3.1-5.7 ppm in DM, respectively. Increasing N contents, whether due to N applications or P or K deficiency, decreased the content of all essential and some other amino acids in crude protein. Both S and severe P deficiency had a pronounced negative effect on amino acid composition and chemical score. Only glutamic acid (glutamine) and arginine were increased by increasing N contents. However, expressed as g/kg DM the concentrations of all amino acids were positively correlated with protein content. S and P deficiency reduced total dietary fibre (TDF) content of DM from 28.3 to 18.6% and 17.4%, respectively, of which between 53 and 60% were insoluble dietary fibre (IDF). Digestible energy (DE) was positively correlated with protein content (r = 0.90**). In N-balance trials with rats, increasing protein concentrations (50% of total protein given as casein and supplemented with 1% methionine) raised the true digestibility (TD) of the protein from 44 to 72%. The biological value (BV) of protein was generally high, with a mean of 91.7. N deficiency tended to increase and S deficiency tended to decrease the BV.

The apparent digestibility of energy, protein, fat and nonstarch polysaccharides (NSP) of a low fiber diet and two high fiber diets containing coarse or fine whole meal rye bread was studied in experiments with humans and rats. Human subjects consumed the experimental diets for 3 wk each in a 3 x 3 cross over design. For the rat diets, duplicate portions of the foods consumed by the human subjects were mixed together, freeze dried and ground. There was a good agreement in the digestibility of energy (humans: 94.7 +/- 0.9, 91.2 +/- 1.2 and 91.6 +/- 1.4%; rats: 95.0 +/- 0.8, 92.5 +/- 1.4 and 91.7 +/- 1.8%) and fat (humans: 95.2 +/- 1.5, 94.4 +/- 1.0 and 94.8 +/- 2.5%, rats: 95.4 +/- 0.9, 94.0 +/- 0.4 and 94.0 +/- 0.4%) for the low fiber diet and the diets containing coarse or fine whole meal bread, respectively. Apparent and true digestibility of protein was consistently lower (P < 0.0001) in humans (apparent digestibility: 90.6 +/- 1.5, 86.2 +/- 1.4 and 86.3 +/- 2.3%; true digestibility: 95.1 +/- 1.5, 90.7 +/- 1.4 and 90.8 +/- 2.2%) than in rats (apparent digestibility: 92.3 +/- 1.1, 89.4 +/- 0.9 and 88.9 +/- 1.0%; true digestibility: 98.3 +/- 1.1, 94.9 +/- 0.9 and 94.2 +/- 1.0%) for all three diets. The digestibility of NSP tended to be lower (P < 0.066) in rats than in humans for the diet containing fine whole meal bread (rats: 59.6 +/- 8.0%, humans: 68.0 +/- 5.2%) and the low fiber diet (rats: 72.1 +/- 10.8%; humans: 80.5 +/- 7.1%), whereas it was similar in both species for the diet containing the coarse whole meal bread (rats: 66.1 +/- 6.0%; humans: 65.8 +/- 9.3%). In spite of some differences in digestibility values, our results suggest that the rat is a suitable model for humans to predict digestibility of nutrients in mixed diets containing cereal fiber sources.

In balanced experiments with rats the influence of the period of adaptation on nutrient digestibility in diets containing cellulose (CEL), guar gum (GG), pectin (PEC) or retrograded high amylose maize starch (RS) was studied. Inclusion level was 80 g/kg diet DM except for the retrograded high-amylose maize starch, where the level was 316 g/kg diet DM. A diet containing normal maize starch only acted as a control diet (FF). The apparent digestibilities of DM, NSP, starch and protein were determined after adaptation periods of 4 d and 2, 4, 6 and 8 weeks. The digestibility of nutrients was affected by diet (P < 0.001) as well as by the period of adaptation (P < 0.001). The digestibilities of DM, NSP and starch increased asymptotically during the course of the experiment. The asymptotic progress over time was most pronounced for the GG, PEC and RS diets. The estimated periods of adaptation required for stable DM digestibility were approximately 1 week for the GG, PEC and RS diets and < 4 d for the FF and CEL diets. The digestibility of NSP in the GG and PEC diets was also stable after approximately 1 week, while it was stable from < 4 d for the CEL diet. However, PEC increased the faecal content of uronic acids for at least 2 weeks. A stable starch digestibility required 1 month in the case of RS and 3-10 d for the other diets. The high faecal content of glucose for the RS diet decreased during all 8 weeks but was still high at the close of the experiment. The apparent protein digestibility changed over time in a parabolic rather than an asymptotic fashion. The GG, PEC and RS diets increased the amount of N excreted by the faecal route.

The performance of methods to determine energy conversion factors for dietary fibre (DF) supplements and fermentability (D) values of their non-starch polysaccharides (NSP) was investigated. Heats of combustion, digestible energy (DE) and D values were determined on five DF supplements in five European laboratories on five separate occasions. In each instance the DF supplements were fed to juvenile male Wistar rats at two doses, 50 and 100 g/kg basal diet, for 3 weeks with food and faeces collected in the 3rd week. Among-laboratory variations in heats of combustion (delta Hc) were < 2%. DE values (kJ/g dry weight) at the upper and lower doses respectively were: 10.4 and 9.9 for a high-methoxyl apple pectin, 9.5 and 9.4 for a sugar-beet DF supplement, 12.2 and 12.7 for soyabean DF supplement, 3.8 and 4.0 for maize bran, and 0.3 and 0.3 for Solka-floc cellulose. Variations among laboratories, among occasions and among animals were < 1, < 2 and < 2.5 kJ/g respectively. The among-occasion: among-laboratory variance ratio for DE was 0.5, suggesting the method performed equally well in all laboratories. There was no evidence of learning of fatigue or fatigue in the performance of the method. D values were also independent of dose and at the high and lower doses were: pectin 0.92 and 0.95, sugar-beet NSP 0.68 and 0.68, soyabean NSP 0.86 and 0.88, maize bran 0.17 and 0.18, cellulose 0.07 and 0.06. Among-laboratory variance tended to increase with decreasing fermentability and ranged from 0.03 to 0.18. The DE and D data were not significantly different from a previously proposed relationship DE = 0.7 x delta Hc x D, where delta Hc is the heat of combustion of the supplement. We conclude that while the among-laboratory variation in the D of difficult-to-ferment NSP is too large for the reliable prediction of energy value the method for the direction determination of DE is both reproducible and repeatable, that DE is independent of dosage of DF supplement up to 100 g/kg diet, and that it is safe to discriminate between energy values with a precision of 3 kJ/g. The conversion of both DE and D to net metabolizable energy for the purpose of food labelling, tables and databases is described.

The present study was undertaken to provide detailed information on the effect of dietary fibre (DF) level on body composition, visceral organ weight, nutrient digestibility and on energy and protein metabolism of rats housed in cold (16 degrees), warm (24 degrees) or hot (32 degrees) thermal environments. High- or low-fibre diets (257 v. 56 g DF/kg dry matter (DM)) were studied in a 6-week balance experiment (initial body weight about 100 g). Heat production was measured using open-air circuit respiration chambers. Pea fibre and pectin were used to adjust the DF level in the high-fibre diet. The ranking order of daily gain of rats kept in different environments was: 24 degrees > 16 degrees > 32 degrees, while the ranking order for carcass protein was: 16 degrees > 24 degrees > 32 degrees. Rats on the high-DF diet had a lower daily gain than those on the low DF diet, and more protein in DM of empty body weight (EBW) and less fat. The relative weights (g/kg EBW) of liver, heart and kidney decreased when increasing the environmental temperature. The relative weight of the heart was highest in rats on the high DF level, while liver and kidney weights were unaffected by DF. Per kg EBW, the stomach, small intestine, caecum and colon and the length of colon were significantly greater in rats consuming the high-fibre diet compared with those on the low-fibre diet. Rats kept at low temperature had a significantly heavier gastrointestinal (GI) tract than those kept at the highest temperature. Digestibility of protein, DM and energy was lowest for rats fed on the high-fibre diet. Heat production (HP) of fed rats as well as fasting HP decreased significantly as environmental temperature increased. HP as a proportion of metabolizable energy (ME) was significantly lower for rats at 24 degrees compared with the other environmental temperatures. The proportion of energy retained as protein was slightly higher in rats fed on the high-fibre than on the low-fibre diet. Based on the results of the present study the authors measured a net energy value of 5.4 kJ/g DF fermented; approximately 50% of the DF came from peas. Possible implications of the present findings are discussed.

Current knowledge of the effects of dietary fibre and associated components on protein digestibility and utilization are discussed. Based on the literature it could be shown that the implications and mechanisms behind the effect of soluble and insoluble dietary fibre on protein digestibility and utilization are quite different. Insoluble dietary fibre will increase faecal bulk and faecal nitrogen excretion is primarily due to and increased excretion of cell wall bound protein. Contrary to this, soluble dietary fibre increase faecal bulk and faecal nitrogen due to an increased excretion of microbial nitrogen. A matter of controversy is the influence of dietary fibre on endogenous nitrogen excretion and factors affecting the losses of nitrogen in this way. It is not known if fibre acts as a secretogogue.

In pot experiments, S-deficiency decreased the seed weight of rape from 4.30 to 2.44 g/1000 seeds at highest N-level. N/S ratios varied from 5.8 to 45.0 and from 3.7 to 21.6 in ryegrass and kale. S-deficiency tended to decrease the fat(oil) content. In kale and ryegrass, it was increased by N-applications, but decreased in rape. S-deficiency had very little effect on starch and sugar content, whereas N-deficiency in kale greatly increased starch (eightfold) and sugar content. Soluble (SDF) and insoluble dietary fibre (IDF) content was hardly affected by S-deficiency. In kale and ryegrass N-deficiency decreased SDF-content, but increased IDF-content. Cystine and methionine concentrations (g/16 g N) were affected by S-deficiency, most strongly at high N-levels, where decreases in kale, ryegrass, rape and field beans amounted to respectively 18, 39, 40 and 17% for cystine and 27, 59, 24 and 6% for methionine. Also, lysine, threonine and tryptophan were decreased. S-deficiency increased aspartic acid (asparagine) content of ryegrass (fourfold) and of arginine in rape and kale. In N-balance trials with rats, S-deficiency reduced the biological value (BV) of the protein of kale from 65 to 40 and of field bean seed from 70 to 61. Corresponding decreases in digestible energy (DE) were from 56 to 48 and from 82 to 78, respectively.

The gastrointestinal (GI) effects of three different dietary fibre (DF) sources: wheat bran (WB), oat bran (OB) and pea fibre (PF), were compared with a low-fibre diet in a 4-week trial with rats (initial bodyweight 210 g). The DF sources varied widely in chemical composition, solubility and water-holding properties, and particle size. The DF sources were mixed into diets to comprise the same amount of non-starch polysaccharides (NSP; 135 g/kg dry matter (DM)). Compared with the control diet, all fibre-containing diets reduced apparent digestibility of DM, energy, and protein significantly but to different extents. The ranking order of faecal DM bulking followed that of NSP recovery in the faeces: WB > OB > PF > control. The elongating effect of the diets on the GI tract was most pronounced in the rats fed on the OB diet. The mean transit time (MTT) of the OB diet was similar to that of the control diet (approximately 37 h), which was significantly slower than the MTT of the WB and PF diets (approximately 23 h). The study confirms that no simple cause and effect relationship exists between chemical composition, physical properties, and physiological effects of dietary fibre and their effects along the GI tract.

Digestibility of dietary fibre (DF) and energy of three pale-seeded and one dark-seeded variety of Amaranthus caudatus were studied in balance experiments with growing rats. Effects of processing: popping, toasting and flaking were also examined. The pale seeds contained about 8% of DF and the black seeds about twice as much. The soluble DF fraction made up 33-44% of the total DF (TDF) fraction in the pale-seeded varieties, but only 18% in the black seeds. The monomer sugar composition of the DF was very similar in all products. However, the black seeds were very high in lignin, and DF of the black-seeded products were more resistant to digestion than that of the pale-coloured products. In the pale amaranth products digestible energy (DE) varied between 86 and 91%. In the dark-seeded products DE was lower, and there was a significant negative correlation (r = -0.92) between DE and TDF. Processing of pale seeds had only minor effects on TDF and DE, but increased the proportion of soluble DF and the digestibility of DF in one variety. The food intake tended to be lower in rats fed raw pale seeds compared with those consuming processed products, indicating the presence of heat-labile factors reducing palatability. In conclusion, the pale seeds had a lower content of DF than most cereal grains and the DF was more easily digested. As a source of energy, amaranth grains seem to be comparable to other cereals.

1. The present work with growing rats was undertaken to compare the effect of wheat bran and barley husk on nutrient bioavailability. The experiment involved a total of nine dietary treatments consisting of a control group, without wheat bran or barley husk, and two series of four groups with increasing amounts of fibre from 50 to 117 g/kg dry matter (DM) from the two fibre sources. Dietary nitrogen concentration was kept constant at 15 gN/kg DM by adjusting the diets with an N-free mixture. Protein sources were casein, fortified with methionine and white wheat flour. True protein digestibility (TD), biological value (BV), net protein utilization (NPU) and digestible energy (DE) were estimated. 2. TD decreased when total dietary fibre (TDF) increased, the effect being greater in the case of wheat bran. The difference in response can be explained by the larger N contribution from bran than from barley husk. N from barley husk was actually digested less than N from wheat bran. 3. Changes in TD due to fibre were small, both for wheat and barley husk. It was concluded that decreased TD with fibre at moderate levels was due to poor digestibility of the N associated with the fibre source rather than decreased digestibility of N from other dietary components. 4. BV was only marginally affected by the fibre levels, indicating that the relatively high lysine content in both wheat bran and barley husk had a low availability. 5. Wheat bran and barley husk showed almost the same negative effect on DE and DM digestibility (DMD). DMD correlated significantly with DE, demonstrating that DMD is a simple and convenient means of monitoring DE.

Two nitrogen-balance experiments were performed with growing rats to test the effect of dietary fibre level, protein quality and antibiotic inclusion on microbial activity, N excretion patterns and energy digestibility. Each experiments involved eight dietary treatments in a 2 X 2 X 2 factorial design, with five rats per treatment. The eight treatments resulted from a combination of two protein treatments, two fibre treatments and two antibiotic treatments. In Expt 1 the protein was provided as barley, or barley plus 2 g L-lysine hydrochloride/kg dry matter (DM) (at 15 g N/kg DM) and in Expt 2 as soya-bean meal or soya-bean meal plus 2 g DL-methionine/kg DM (at 15 g N/kg DM). In both experiments the basal diet was provided with or without additional fibre as 100 g barley husk/kg DM and with or without antibiotic as 7 g Nebacitin/kg DM. With both barley and soya-bean meal, true protein digestibility (TD) was improved with the addition of amino acids. Only with the soya-bean meal diets was TD increased with Nebacitin treatment, with the effect of Nebacitin and methionine being additive. Barley husk slightly reduced the TD of soya-bean meal. The effect of treatments on biological value (BV) was considerable. Lysine increased BV of the barley diet from 0.741 to 0.815 whereas Nebacitin reduced BV from 0.799 to 0.757. Methionine increased the BV of soya-bean meal from 0.754 to 0.911 while BV was reduced by Nebacitin from 0.843 to 0.821 and by barley husk from 0.845 to 0.820.(ABSTRACT TRUNCATED AT 250 WORDS)

1. Three series of nitrogen balance experiments were performed with growing rats to test the effect of type and level of protein, fibre and starch on N excretion patterns. The design involved eighteen treatments in a 3 X 3 X 2 factorial experiment with five rats per dietary treatment. The eighteen treatments resulted from a combination of three protein treatments, three fibre treatments and two starch treatments. Protein treatments consisted of one level (15 g N/kg DM) of casein fortified with methionine, a protein of high digestibility, and two levels (15 and 20 g N/kg DM) of autoclaved brown beans (Phaseolus vulgaris), a protein source of low digestibility. The fibre treatments were two levels of cellulose powder and one level of barley hulls. The two starch treatments were autoclaved potato starch and autoclaved and raw potato starch (1:1, w/w). 2. The inclusion of raw potato starch reduced true protein digestibility markedly when the protein source was casein, but the corresponding biological values were increased significantly with this treatment. This strongly indicated a movement of urea from the blood to the intestines. This assumption was also supported by significantly lower blood urea concentrations in animals given raw starch. The influence of raw starch on true protein digestibility was, however, significantly less when cellulose and barley hulls were included. This is probably due to reduced transit time from fibre inclusion. The nature of the gut contents also supported this hypothesis. 3. The inclusion of raw potato starch when brown beans were the source of protein had much less effect on true protein digestibility and biological value than when casein was the protein source. This was probably due to the low digestibility of DM and protein in this food leaving sufficient energy and protein for maximum microbial growth. The inclusion of fibre also had little effect on N excretion patterns with the brown-bean diets. 4. An increase in the level of brown bean inclusion reduced true protein digestibility only on the diets containing raw starch whereas the biological value was consistently reduced regardless of starch treatment. The lower biological values were associated with significantly higher blood urea concentrations. Increasing the level of brown bean inclusion also resulted in higher fresh weights of caecum, colon and contents. 5. The present work proves that, through dietary manipulation, it is possible to affect nitrogen excretion patterns in rats.

1. The experiment was designed to investigate the effect of protein level in diets on apparent protein digestibility (AD), true protein digestibility (TD), biological value (BV), net protein utilization (NPU) and energy digestibility (DE) in rats. The design involved fourteen dietary treatments in which a combination of wheat bran and meat-and-bone meal (1:1, w/w dry matter (DM) basis) was the only nitrogen source. Crude protein (N x 6.25; CP) level ranged from 60 to 329 g/kg DM in approximately even increments. All diets contained a constant level of minerals and vitamins. The balance of the diet consisted of a N-free mixture. 2. AD increased from 0.602 at 60 g CP/kg DM to 0.702 at 120 g CP/kg DM, with little change at the higher levels of dietary protein. The fitting of a curve indicated an asymptote of 0.721. 3. TD did not vary significantly between 60 and 225 g CP/kg DM (mean 0.781). At the higher protein levels there was a slight but significant reduction in the mean value (0.758). 4. BV increased from 0.475 at 60 g CP/kg DM to 0.498 at 80 g CP/kg DM where it plateaued, and then from 160 g CP/kg DM it decreased at an increasing rate to 0.216 at 329 g CP/kg DM. 5. The response in NPU closely reflected that obtained with BV, rising from 0.370 to 0.384, then declining to 0.162 at the highest CP concentration. 6. DE decreased linearly from 0.851 at 60 g CP/kg DM to 0.617 at 329 g CP/kg DM. 7. The results confirmed that AD values should only be compared at a defined protein level. TD was essentially independent of dietary CP level, except for a small reduction above 250 g CP/kg, whereas BV and NPU were stable only within the range 80-140 g CP/kg DM. DE was negatively related to dietary CP and fibre level.

1. The present work was undertaken to study comparatively the effect on mineral availability in rats of wheat bran and barley husk when supplying the same amount of dietary fibre (DF). The experiment involved a total of nine dietary treatments including a control group and two series of four groups with increasing amounts of fibre from the two sources (total DF ranging from 42 to 117 g/kg dry matter (DM]. Dietary nitrogen concentration was kept constant at 15 g N/kg DM. Zinc concentration of the diets was adjusted to the level provided by the diet with the highest wheat-bran content (21 mg/kg DM) using zinc sulphate. Other minerals were not adjusted. 2. Two experiments were performed. In Expt 1 the diets were given to 5-week-old rats during 9 d and apparent absorptions of Zn, calcium and phosphorus and the femur concentrations of Zn, Ca and P were measured. In Expt 2 the diets were given to 9-week-old rats during 12 d. Mineral concentration in femur and total and albumin-bound plasma Zn and availability of plasma Zn for enzyme reactivation were measured. 3. In the younger animals, wheat bran depressed significantly the absorption of Zn when providing 40 g DF/kg DM and absorbtion of Ca when providing 80 g DF/kg DM. Barley husk depressed significantly both the absorption of Zn and Ca already at 20 g DF/kg DM. Both fibre sources had a more negative effect on Zn than on Ca absorption. Only barley husk had a small negative effect on absorption of P. Phytate did not appear as a major factor affecting mineral absorption in barley husk. All diets containing barley husk had a very low molar ratio, phytate:Zn. 4. The age of the animals influenced the utilization of dietary minerals using femur concentration as a criterion, particularly in the case of Zn. In the younger animals the decrease in femur Zn with fibre correlated with apparent Zn absorption both with wheat bran (R2 0.986, P less than 0.01) and with barley husk (R2 0.996, P less than 0.01). In the older animals femur Zn did not change significantly with fibre. 5. In the older animals, plasma Zn, albumin-bound plasma Zn and availability of plasma Zn for enzyme reactivation were lowest with the highest addition of wheat bran.

Four new high-lysine barley mutants, the variety 'Lysimax', with the high-lysine gene lys3a and the mutants mother variety 'Sultan' were grown in a field trial in 1993 at Risø, Denmark. Mutants 609, 1242, 1385 and 1405 yielded in the range of 89 to 98 percent and cv 'Lysimax' yielded 102 percent of cv 'Sultan' (100 percent). One-thousand kernel weights for the mutants were in the range of 87 to 97 percent and cv 'Lysimax' 83 percent of cv 'Sultan' (100 percent). Protein contents of the mutants were slightly higher, in the range of 13.2 to 13.6 percent, than of cv 'Sultan' (13.1 percent) and 'Lysimax' which had a protein content of 12.6 percent. Fat content was higher in 'Lysimax' and in the mutants except for mutant 1385 than in cv 'Sultan' while dietary fibre contents of the barleys were similar. The levels of beta-glucans and starch were usually lower in 'Lysimax' and in the mutants. The highest lysine levels: 4.6, 4.0 and 3.7 g/16 g N occurred in cv 'Lysimax' and mutants 609 and 1405 compared to 3.3, 3.3 and 3.2 for cv 'Sultan' and mutants 1242 and 1385, respectively. Mutants 609 and 1405 and cv 'Lysimax' also had higher levels of threonine, histidine and valine. The increased lysine contents resulted in large, at most 20 percent, increases in biological value; 88.8, 81.7 and 78.3 percent for cv 'Lysimax' and mutants 609 and 1405 compared to 74.2 percent for cv 'Sultan'. True protein digestibilities and energy digestibilities were slightly lower in 'Lysimax' than in 'Sultan', 5.3 and 4.3 percentage units, respectively. It is concluded that the development of high-lysine barley varieties is very beneficial for meeting the requirements of indispensable amino acids for humans and monogastric animals. In addition, nitrogen excretion into the environment is drastically reduced due to the higher biological values of the mutants. [ABSTRACT FROM AUTHOR]

Crisphead lettuce was cultivated under different growth conditions. Sixteen batches differed in time of planting (early and late), total nitrogen supply (200 kg N/ha, 150 kg N/ha, 100 kg N/ha, 50 kg N/ha) and time of harvest (early and late). Based on chemical analysis and balance studies on rats the nutritive value of each 16 batches was determined. The protein content increased progressively from 16.00 to 19.88% with fertilization level. This increase in protein caused a significant drop in essential amino acids (g/16 g N) demonstrating a lower biological value of this protein. Early planting or early harvest resulted in a higher protein content than in lettuce of late planting or late harvest. Total dietary fibre content was approximately 25% of DM-and this value was not much influenced by the different growth conditions. Soluble dietary fibre was approximately 20-25% of total dietary fibre. Due to the high fibre content, energy digestibility was relatively low. The contents of Cd and Pb were below what is considered as 'acceptable' levels. [ABSTRACT FROM AUTHOR]