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Biomedical subjects

O Simon

Publications and source records attributed to O Simon.

At least 73 records · Page 4Linked to original sources
PubMed1986

[Nitrogen metabolism in the large intestine of ruminants. 2. Metabolism of i.v. infused 15N-urea by additional supply of fermentable material to the large intestine of bulls].

The experiment was carried out on 3 bulls with body weights of 201, 168 and 190 kg, respectively. The animals were equipped with a ileo caecal re-entrant cannula and with catheters in the jugular veins on both sides. The pelleted ration was composed of straw 70-72%, cereals 10%, molasses 12-41%, ammoniumhydrogencarbonate 3%, urea 2% and mineral mixture 1%. During a preliminary period ileal digesta were collected, deep-freezed and stored. During the main experiment 15N-urea was infused intravenously for 24 hours. In this period and during the following 6 hours outflowing ideal digesta were collected quantitatively. At the same time precollected, unlabelled digesta together with a supplement of partly hydrolysed straw meal were reintroduced into the caecal part of the cannula. Plasma urea-N, urinary-N as well as several N-fractions of faeces and digesta were analysed for 15N abundance. A urea flux rate of 27.9 +/- 3.4 mumol per minute per kg 0.75 was estimated. It was calculated that 52% of this amount of urea was transferred into the digestive tract. In both, digesta and faeces NH3-N was highest 15N-labelled indicating a direct urea entry and degradation in both segments of the digestive tract. The amounts of 15N-excess found during the period of digesta replacement were in faeces 0.25 and in ileal digesta 4.02% of the infused amount of 15N. Although the microbial utilization of endogenous urea-N was generally low in the large intestine there was a clear stimulation of this process due to the additional supply of the large intestine with a fermentable source.

Animals↗
PubMed1986

[Nitrogen exchange in the large intestine of ruminants. 4. Exchange and isotope balance of intracecally administered 14C- and 15N-urea in sheep with simultaneous intracecal dose of a partly hydrolyzed straw meal].

Two experiments were performed with wethers (Body weight 34 to 44 kg) receiving a ration rich in crude fibre at maintenance level. The animals were fitted with ileocaecal cannulas into which 14C-, 15N-labelled urea together with digesta was introduced hourly for a 24 hours period (V1; 2 animals). In experiment two (V2; 3 animals) in addition HCl-partly hydrolysed straw meal was introduced. After ureolytic degradation the intracaecal applied urea entered mainly the intermediary metabolism. The resulting ammonia was resynthesized to urea without any time lag. The rate constant for the increase in 15N labelling of urea was 3.2 d-1 in both experiments. Urea leaves the plasma with half lives of 10.6 (V1) and 5.2 (V2) hours. More than 60% of the applied urea were excreted with urine. Formed 14CO2 appeared at proportions of 66% (V2) and 71% (V1) in the respiration gases. Both, the decline of the 14C-activity in blood plasma and the specific 14C-activity of CO2 in the respiration gases after the end of the labelling period do not follow a kinetic of first order. The 15N-labelling of the NH3-N in ileal digesta was very high and reached plateau values similar with those of plasma urea (2.54 vs. 2.56 atom-% 15N-excess). A direct entry of plasma urea into the small intestine was concluded.

Animals↗
PubMed1986

[Nitrogen metabolism in the large intestine of ruminants. 3. Microbial utilization of intracecally administered 14C- and 15N-marked urea in the large intestine of sheep in simultaneous intracecal administration of partially hydrolyzed straw meal].

Two experiments were performed on sheep, receiving on maintenance level a pelleted straw ration high in crude fibre (straw, 70.5%; dried sugar beet pulp, 12%; cereals, 10%; urea, 2%; ammonium hydrogen carbonate, 3%; minerals 2,5%). The animals were fitted with ileo-caecal re-entrant cannulas. The effects of the introduction of HC1-partly hydrolysed straw meal into the digesta of the large intestine on the digestion processes in that segment were studied. Under these conditions the metabolism of 14C and 15N labelled urea, which was given into the caecum, was estimated. In experiment 1 (E 1; 2 animals) unlabelled, precollected digesta were hourly reintroduced together with 14C and 15N labelled urea via the caecal cannula. In experiment 2 (E 2; 3 animals) the digesta were supplemented with partly hydrolysed straw meal (10% of the mean daily DM-intake with the ration). The supplement of partly hydrolysed straw meal caused an increase of the 15N excretion with faeces from 13.4% (E 1) to 19.8% (E 2) of the dose. The 15N was mainly incorporated in the bacterial fraction (98% E 1; 96% E 2). As a reason for the increased 15N incorporation into the bacterial fraction of 106.4 mg15N' in E 2 vs. 67.3 mg15N' in the experiment without straw meal supplement the higher supply of energy as fermentable carbohydrates was assumed.

Animals↗
PubMed1985

[Nitrogen metabolism in the large intestine of ruminants. 1. Metabolism of i.v. infused 15N-urea without additional carbohydrate supply to the large intestine].

The experiments were carried out on 3 bulls (body weight: 172, 229 and 193 kg), equipped with ileo-caecal cannulas and with catheters in the jugular veins on both sides. The offered pelleted ration consisted of straw 73%, molasses 12%, cereals 10%, ammonium hydrogen carbonate 3% and urea 2%. Feed intake amounted to about 3 kg per animal and day. During a preliminary period of 5 days 50% of ileal digesta were collected for 12 hours daily, deep-freezed and stored. In the main experiment 15N-urea was infused intravenously for 24 hours. During this period and during the following 6 hours ileal digesta were collected and replaced by precollected, unlabelled digesta. The urea metabolism was estimated by the 15N-labelling of blood urea, by the 15N-excretion via faeces and urea, by the appearance of 15N in ileal digesta and by the 15N-labelling of faecal NAN, NH3 and bacterial fraction. The time course of the 15N-labelling of plasma urea during infusion can be described by an exponential function. The urea flux rate was estimated from the calculated plateau value. The flux rate for the 3 animals was 28.8, 30.7 and 34.8 mumol per minute per kg0.75, respectively. During the infusion of 15N-urea 1.0-2.4% of the infused amount of 15N' appeared in ileal digesta, half of it in the TCA precipitable fraction. At the same time the 15N-labelling of faecal NH3 increased sharply, however, the 15N-labelling of the faecal bacterial fraction was smaller by one order of magnitude. Deficiency of fermentable substrates and problems of inhomogenity of the NH3 pool are supposed as reasons for this result. 30 to 50% of the urea flux entered the digestive tract, the direct entry of urea into the large intestine seems to be only very low.

Animal Feed↗
PubMed1985

[Effect of glutamic acid content in the diet on the catabolic rate of the isotope-labeled glutamic acid in rats. 4. Measurement of 14C-glutamic acid oxidation to 14CO2 with various energy sources in the diet].

48 male rats (body weight 80-100 g) were fed with 2 diets different in the glutamic acid content (diet I 2.42 and diet II 6.24% glutamic acid in the dry matter). The mixture of the other synthetic L-amino acids was adapted to the egg protein pattern corresponding 10% crude protein in the diet. Each diet was fed either on 73% or 98 to 104% of the energy maintenance requirement. After 7 days of experimental feeding 14C-U-L-glutamic acid was given to each group by intragastric infusion (i.g.), intraperitoneal (i.p.) or subcutaneous injection (s.c.), respectively, followed by a measurement of the CO2-and 14CO2-excretion during two subsequent periods of 3 hours. The CO2-excretion was lower in animals with restricted energy intake especially during the first 3 hour-period, which was started 2 hours after feed intake. The relative 14CO2-excretion (percent of the dose) was neither significantly influenced by the level of energy intake nor by the amount of dietary glutamic acid. The highest degradation rates of 14C-glutamic acid to 14CO2 were measured after i.g. application (more than 50%), followed by the i.p. injection (nearly 50%) and the lowest values were observed after s.c. injection (about 40%). These differences were only evident during the first CO2-absorption period. Furthermore the s.c. injection caused a lower specific radioactivity of CO2 compared with the data after i.g. and i.p. application. The results suggest the high metabolic activity of the intestinal tissue for glutamic acid.

Animal Feed↗
PubMed1985

Effect of spinning and additional cross-linking with dialdehyde starch or aluminum ions on the digestibility and quality of casein-Vicia faba protein isolate mixtures.

Studies were made in adult rats using an isotopic 15N method. Whole egg, wheat, casein and Vicia faba protein isolate served as reference proteins. The diets were isonitrogenous and feed intake was adjusted to the maintenance energy level. Variations in true N digestibility were small (91.8-96.1%). The amount of metabolic fecal nitrogen in animals receiving the diet containing wheat was 9.4 mg/100 g body weight compared with 4.9-5.8 mg in the other diets. The differences in nutritional quality for maintenance between proteins of plant and animal origin were small. However, spinning (alkaline treatment) and additional cross-linking with aluminum ions or dialdehyde starch affected the nutritional quality for maintenance.

Aluminum↗
PubMed1984

The structure of wakefulness and its relationship to daytime sleep in narcoleptic patients.

Seven patients with narcolepsy-cataplexy were continuously monitored during the day using polygraphy and videotape recording. The patients were free to do whatever they wanted while confined to a sitting-at-a-table situation. Daytime activity was evaluated by distinguishing between two polygraphically defined states, namely active wakefulness and quiet wakefulness. The data from the patients were compared with those from 7 normal subjects who were studied under the same experimental conditions. While all patients had recurrent daytime sleep episodes, none of the controls napped during the recording period. The narcoleptic patients showed an altered structure of wakefulness: they spent more of their time awake in the state of active wakefulness and less in quiet wakefulness than the control subjects. Moreover, the patients remained in the quiet state for shorter periods. Daytime sleep selectively diminished the state of quiet wakefulness, whereas it did not affect the amount of time spent in active wakefulness. In addition, in 3 patients there was a clear-cut alternation of periods of sustained wakefulness and transitional phases with a mixture of sleep and wakefulness which occurred rather regularly, suggesting an ultradian cycle of sleepiness.

Adult↗
PubMed1984

[Endogenous nitrogen metabolism in 15N-labeled swine. 3. Endogenous excretion of 15N- and 14C-labeled secretions following a 14C-leucine injection].

Four pigs (59-65 kg live weight) were labelled over a period of 10 days with 15N in the feeding of a fishmeal diet (1), a fishmeal diet + partly hydrolysed straw meal (2), a horse bean diet (3) and a horse bean diet + partly hydrolysed straw meal (4). After a 24-hour fasting the animals were provided with simple cannulae in the upper part of the small intestines. After a fasting period of 24 h all four pigs received a 14C-leucine injection and the cannula secretion was collected in the subsequent 24 h. After the feeding of the diets without straw meal supplement (1 and 3) there were distinct differences in the secretion in comparison with the feeding with straw meal supplements (2 and 4) despite the long fasting period (48-72 h). 14C-activity could already be detected in the TCA-precipitable fraction of the secretion after 3-6 min of the injection in 1 and 3 but only 20 to 25 min after the 14C-leucine injection in 2 and 4. The specific 14C-leucine activity of the TCA-soluble fraction of the secretion was, after the straw meal supplementation to the fish meal diet, 15 times higher 25 min after the 14C-leu-injection, 25 times higher after 70 min, 36 times after 2 h and 1.8 times after 4 h than without straw meal supplementation. For all four diets a specific correlation (r = 0.96) could be ascertained between the increase of 14C-activity/mg N in the TCA-soluble fraction and the increasing crude fibre content in the diet between 25 and 180 min after the injection. Furthermore, a distinctly decreased N-secretion/h could be ascertained (correlation coefficient r = 0.84) with the increasing crude fibre content in the diet. The influence of the crude fibre on the parameters mentioned is seen in the changed osmotic conditions in the secretion, which may be caused by the changed regulation by hormones of the gastro-intestinal tract. The atom-% 15N' in both TCA-fractions of the secretion underwent big rhythmic variations, which is explained by different ratios of the components pancreatic juice, bile, and intestinal juice.

Animal Feed↗
PubMed1984

[Effect of glutamic acid content of the diet on isotope-labeled glutamic acid catabolism in rats. 1. The course of 14CO excretion following intragastric administration of 14C-glutamic acid].

Male rats received in 8 groups of 10 animals each for a period of 7 days 7 synthetic diets and one semisynthetic diet on maintenance requirement level. A L-amino acid mixture corresponding to the pattern of egg protein without glutamic acid was the protein source of the synthetic diets. Glutamic acid was supplemented successively from 0 to 58 mol-% of the total amino acid content. The crude protein source of diet 8 was whole egg powder. On the 8th day of experiment 5 animals per group were labelled by intragastric infusion (i.g.) with 14C-U-glutamic acid. During the following 24 hours the excretion of CO2 and 14CO2 was measured. Throughout the experimental feeding body weight was relative constant, however, when the synthetic diets were fed it was necessary to increase the daily amount of energy from 460 to 480 kJ/kg0,67. The relative 14CO2-excretion within 24 hours was 68-75% of the dose. However, the main part of the amount of radioactivity excreted during 24 hours was found after 4 to 6 hours already. Exponential functions calculated from the data of cumulative 14CO2-excretion suggest the existence of a fast process of 14CO2-formation directly from 14C-glutamic acid, reaching a plateau within 2 hours and a slow process of oxidation of intermediates of glutamic acid metabolism, causing a continued 14CO2-formation even after 24 hours. The oxidation of 14C-glutamic acid to CO2 decreased 2 to 14 hours after i.g. labelling if the glutamic acid content of the diet increased. The same was found for the specific radioactivity of 14CO2. A storage of intermediates of glutamic acid before degradation was assumed.

Animals↗
PubMed1984

[Effect of glutamic acid content of the diet on the catabolic rate of isotope-labeled glutamic acid in rats. 2. Time course of 14CO2 excretion following subcutaneous administration of 14C-glutamic acid].

40 rats with a body weight of 100 g received 7 semisynthetic diets with different contents of glutamic acid and one diet contained whole egg. A L-amino acid mixture corresponding to the pattern of egg protein was the protein source of the semisynthetic diets. Glutamic acid was supplemented successively from 0 to 58 mol-% of the total amino acid content. On the 8th day of experimental feeding the animals were labelled by subcutaneous injection of 14C-U-L-glutamic acid. Subsequently the CO2- and the 14CO2-excretion were measured for 24 hours. In this period 64 to 68% of the injected radioactivity were recovered as 14CO2. The curve pattern of 14CO2-excretion indicates two different processes of 14CO2-formation. One characterizing the direct degradation of glutamic acid to CO2 with a high rate constant and a second one with a lower rate constant characterizing the 14CO2-formation via metabolites of glutamic acid. 77% of the total 14CO2-excretion in 24 hours resulted from the direct oxidation of glutamic acid and 23% from the oxidation of intermediates. When 14CO2-formation was measured 10 to 24 hours after injection of 14C-glutamic acid a positive correlation to the content of glutamic acid in the diet was observed. The intestinal tissue contribute considerably to the catabolization of glutamic acid, however, there seems to exist an upper limit for this capacity.

Animal Feed↗
PubMed1984

[Effect of glutamic acid content of the diet on the catabolic rate of isotope-labeled glutamic acid in rats. 3. Determination of 14CO2 and 15N excretion following intragastric infusion of 14C- and 15N-glutamic acid].

Male rats (body weight 100 g) received during a 8 days experimental feeding period diets with different contents in glutamic acid. The daily feed intake was restricted to the energy maintenance level of 460 kJ/kg0.75. The diet contained a mixture of L-amino acids corresponding to the pattern of egg protein except glutamic acid. Glutamic acid was added successively at 10 levels (0 to 14,8% of dry matter) and the resulting diets were fed to groups of 4 animals each. At the end of the experimental feeding period 14C- and 15N-labelled glutamic acid were applied by intragastric infusion. CO2- and 14CO2-excretion was measured during the following 4 hours and the urinary N- and 15N-excretion during the following 24 hours. The CO2-excretion decreased from 53 to 44 mmol CO2/100 g body weight with increasing levels of dietary glutamic acid. This change seems to result from the increasing proportion of amino acids as an energetic fuel. While the amount of oxidized glutamic acid increased with increasing supplements of glutamic acid the relative 14CO2-excretion decreased from 57 to 48% of the applied radioactivity. The urinary 15N-excretion during 24 hours was 31% of the given amount of 15N if no glutamic acid was included in the diet. This proportion increased successively up to 52% in the case of the highest supply of glutamic acid. Because the total N-excretion increased at the same extent as the 15N-excretion a complete mixing of the NH2-groups resulting from glutamic acid due to desamination with the ammonia pool was assumed. No correlation between glutamic acid content of the diet and specific radioactivity of CO2 or atom-% 15N excess of urinary N was observed.

Animal Feed↗
PubMed1984

[Endogenous nitrogen metabolism processes in 15N-labeled swine. 2. Fecal excretion of amino acids and 15N-labeled amino acids with diets differing in crude fiber content].

Four pigs were labelled with 15N-ammonium salt over a period of 10 days in the feeding of a fishmeal diet, a fishmeal diet + partly hydrolysed straw meal, a field bean diet and a field bean diet + partly hydrolysed straw meal. The 14N-amino acids and the 15N-amino acids excreted in faeces showed highly significant correlation coefficients with the increasing content of crude fibre in the diets, which amounted to 3.0, 5.3, 10.0 and 12.1% in the DM. The following sequence was established for the growth angle (tan alpha) of the essential 14N-amino acids: Leu, Lys, Arg, Thr, Phe, Ile, Val, His and of the 15N-amino acids: Lys, Arg, Val, Leu, Ile, Thr, Phe and His. As Lys, His and Thr cannot incorporate 15N in transamination reactions in the intermediate metabolism, their level of labelling was considerable in case of diet 4. Nevertheless, tan alpha is highest for 15N-Lys and lowest for 15N-His. This means that His in contrast to Lys, parallel to increased synthesis, is also increasingly decomposed in the large intestine. In contrast to this, proline was not labelled with 15N even with the highest content of crude fibre in the diet. Despite this, 14N-proline excretion, next to glutamic acid, increased most with the growing content of crude fibre in the diet. Due to the hydrophilic character of glutamic acid and the increased water influx in the large intestine and the increased content of crude fibre in the diet, a growing proline transport parallel to the increased influx of crude fibre and water must be assumed. If the growth angle tan alpha for the excretion of 14N-amino acids is ascertained regressively for a crude fibre content of diet of 10%, one can prove from the proportion of the amino acids and a comparison from literature for faecal bacteria and ileum digesta that the amino acid composition for this measuring point largely corresponds to that of bacteria protein.

Amino Acids↗
PubMed1984

Digestibility and dietary quality of nonacetylated and acetylated Vicia faba proteins in maintenance. Studies on 15N-labelled adult rats.

N digestibility and the dietary quality of a Vicia faba protein isolate as well as of two protein fractions from this isolate, acetylated and nonacetylated, were estimated in 15N-labelled adult rats. For reference, whole egg, casein and wheat were studied. The diets were fed at maintenance energy intake level. Daily metabolic fecal nitrogen estimated by an isotopic method was 5 mg/100 g body weight in animals receiving whole egg, casein, or Vicia faba proteins. When wheat was included in the diet metabolic fecal nitrogen was increased to 140% of this value. True N digestibility of reference proteins was 91-92% and of Vicia faba proteins 95-97%. Protein quality for maintenance was high and similar for all proteins. Acetylation affected neither N digestibility nor protein quality under maintenance conditions.

Acetylation↗
PubMed1983

[Effect of a supplement of partly hydrolized straw meal to a diet of fish meal and horse beans on N balance and amino acid excretion in the feces of swine].

2 test pigs each (male castrated pigs) of an average live weight of 51-71 kg received either a wheat/fish meal diet (Ia) or a wheat/horse bean diet (IIa). Due to a supplement of partly hydrolysed straw meal the crude fibre content was increased from 3.0% (= Ia) to 10.1% (= Ib) and from 5.2% (= IIa) to 12.1% (= IIb) in the dry matter. This straw meal supplement decreased the apparent digestibility of the crude protein in I from 92.5 to 85.7% and in II from 89.0 to 79.0%. N-excretion in faeces/100 g DM-intake followed the regression line: y = 228 + 31.2x(r = 0.98) y = mg N/100 g DM-intake x = % crude fibre in the DM of the diet The excretion in faeces/100 g DM-intake of 15 investigated amino acids, too, in each case showed a significant increase with the rising crude fibre content of the diet. The widest growth angle (tan alpha) of all the essential amino acids investigated was shown by lysine and those amino acids with branched chains. The conclusion is that in the presence of a fermentable crude fibre source and a good N-supply those 4 amino acids show a suitable bacterial synthesis rate and a low decomposition rate.

Amino Acids↗
PubMed1983

[Changes in protein synthesis in the liver and small intestine of rats after feeding].

Rats trained on fast food intake received a combined intravenous injection of [14C]valine and unlabelled valine before and 1, 2, 4 and 6 h after food intake, respectively. The rate of protein synthesis was calculated basing on the average specific radioactivity of free valine in blood plasma and in the analyzed tissues during the 10 min incorporations period and on the specific radioactivity of protein bound valine in the tissues at the end of incorporation time. Before food intake the fractional rate of protein synthesis (ks) in liver was 55-67% per day and increased 1 to 4 h after food ingestion to 80-120% per day. ks in small intestine before food intake amounted to 78-109% per day and no specific changes were observed in time course. The synthesized amount of protein in liver and small intestine (related to 100 g body weight) was found to be 14-19 mg/h before food ingestion. This value increased postprandially in the liver to 25-32 mg/h and decreased towards the end of the testing period to 20-25 mg/h. The stimulation of the rate of protein synthesis in liver and perhaps in other organs may be part of a mechanism delaying the inflow of amino acids into tissues with lower turnover rates.

Animals↗
PubMed1982

[The EEG of patients with acute manic psychoses before, during and after treatment with high doses of d-propranolol and dl-propranolol (author's transl)].

Six manic patients, drug-free for at least 10 days, were treated with high doses (up to 3,000 mg/day, corresponding serum levels up to 1,600 ng/ml) of d-propranolol or dl-propranolol in a double-blind, placebo-controlled study. The EEG's of these patients were studied over a maximum period of 21 days. All 82 EEG's were normal, they showed neither epileptic patterns nor any other signs for hypersynchronisation, as a possible side-effect of propranolol, nor other abnormalities, due to the manic condition. Analysis by fast-fourier-transformation produced no difference between the effect of d-propranolol or dl-propranolol on EEG compared intra- and inter-hemispherically by power-spectra, cross-spectra, phase-differences and coherences. At high serum levels (more than 1,000 ng/ml) there was a corresponding increase of power and a drop in frequency of the alpha-activity, maximally--1.1 c/s, which probably depended on the serum level. This result is in agreement with the hypothesis of a direct antimanic effect of the drug and comparable to the clinical effect of lithium, which produces similar changes in EEG. A comparison of the propranolol-induced EEG changes with EEG changes usually induced by sedative drugs, contradicts the hypothesis that the antimatic properties of propranolol are caused by unspecific sedation.

Adult↗
PubMed1982

Studies on the range of tissue protein synthesis in pigs: the effect of thyroid hormones.

The effects of thyroid hormones on the range of tissue protein synthesis in growing pigs using the constant infusion technique with [14C]lysine were studied. 2. During a 6 h infusion, samples were taken from blood and, at the end of the infusion, from liver, pancreas, stomach, small and large intestines, kidney cortex, kidney medulla, muscle and skin. 3. Lower relative specific radioactivities of free leucine and lysine in several tissues were observed in the hormone-treated group than in the untreated one. 4. The range of protein synthesis rate and the daily amount of protein synthesized in tissues was higher in all tissues after application of thyroid hormones. 5. Assuming that the organs analysed represented 70% of the total trichloroacetic acid-precipitable protein of the pig, the estimated range of daily protein synthesis was 251-490 and 312-880 g in untreated and hormone-treated pigs respectively.

Animals↗