The peculiarities of nitrogen excretion in sturgeons (Acipenser ruthenus) (Pisces,Acipenseridae)—I. the influence of ration size

• 1.1. The nonfaecal nitrogenous excretion rate in starved sterlet fingerlings and fingerlings fed on different rations was investigated. The weight of the fish and temperature of the water was 43 g and 17.5°C, respectively.
• 2.2. In the nonfaecal excrements of starved sterlets the ammonia: urea ratio was substantially lower than in teleosts. This ratio was found to be 1.4:1.
• 3.3. In fed sterlets the urea excretion rate was higher than in starved ones but independent of ration size.
• 4.4. During the day the urea excretion rate in sterlets was constant.
• 5.5. The ammonia excretion rate accelerated 2 hr after feeding and reached its peak duration 6–11 hr after depending on the ration size.
• 6.6. Total ammonia output in the sterlet increased following the increase of ration size up to 8.4% of body wt. Further increases in ration size did not cause the corresponding elevation of ammonia excretion rate.

     

Effects of lysine administration on plasma arginine and on some nitrogenous catabolites in rainbow trout

• 1.1. Rainbow trout were fed either graded levels of lysine (0.8, 1.8 and 3%) at a constant level of arginine (1.4%) or excess arginine (2.4%) at a fixed level of lysine (1.8%).
• 2.2. Increasing the dietary lysine level affected plasma urea, plasma arginine and ammonia excretion.
• 3.3. Trout fed graded levels of lysine received an arginine challenge (U¹⁴C-l-arginine) and it was found that excess dietary lysine led to a decrease in arginine degradation.
• 4.4. Injection of l-lysine induced a decrease in urea excretion, while injection of l-arginine increased both urea and ammonia excretion in control well-fed trout.
• 5.5. These results are discussed in the light of current knowledge on the antagonism between lysine and arginine.

     

The relationship between osmoregulation and nitrogen metabolism in the intertidal prawn,Palaemon elegans (Rathke)

• 1.1. The relationship between nitrogen metabolism and osmoregulation has been studied in the prawn Palaemon elegans (Rathke) following sudden exposure to hyper- and hyposaline conditions.
• 2.2. Animals acclimated to a salinity of 30‰ showed a pronounced increase in the rates of ammonia excretion during the first 2 hr after transfer to lower salinities. These gradually declined during the next 6 hr to rates that were significantly higher than that of control animals (30‰) and were maintained throughout the rest of the experiment.
• 3.3. Rates of ammonia excretion in animals transferred to hypersaline conditions (40‰) fluctuated considerably during the experiment. It was consistently observed, however, that there were two periods during the experiments when ammonia excretion rates had negative values indicating that NH⁺₄ ions were being taken up by the prawns.
• 4.4. Experiments in which small quantities of (NH₄)₂SO₄ containing the stable isotope ¹⁵N were added to the sea-water confirmed that P. elegans was able to take NH⁺₄ ions from the sea-water.
• 5.5. Changes in the Na⁺ ion concentration in the blood and the changes in free amino acid concentration in the blood and in the muscle after exposure to differing salinities were also determined. Their significance and relationship to the observed changes in the rates of ammonia excretion are discussed.

     

Nitrogenous compounds in the excreta of the germfree snail Biomphalaria glabrata (mollusca: Planorbidae)

• 1.1. Nitrogen excretion of germfree snails kept in sterile saline solution during 14 days consists mainly of ammonia and urea in approximately equal amounts.
• 2.2. Uric acid is excreted intermittently being accumulated in snail nephridia.

     

Genetic variation at the Lap locus and ammonia excretion following salinity transfer in an estuarine snail

• 1.1. Thais haemastoma were transferred from 30 to 15‰ and 15 to 30‰ S and ammonia excretion was measured for 72 hr.
• 2.2. Increased ammonia excretion following transfer from high to low salinity was significantly greater in snails with the rare Lap allele, Lap⁹⁴.
• 3.3. Increased rates of nitrogen loss induced by salinity reductions could be responsible for maintaining the Lap⁹⁴ allele at low frequency in estuarine populations of T. haemastoma.

     

The effect of water loss upon the urate,urea and ammonia content of the egg of the Japanese quail Coturnix coturnix japonica

• 1.1. The urate, urea and ammonia content of the whole egg of the Japanese quail was measured in late incubation in eggs subject to different rates of water loss.
• 2.2. High rates of water loss substantially increased egg urate content, but had little or no effect on urea or ammonia content.
• 3.3. Allopurinol, an inhibitor of urate synthesis, reduced egg urate content to low levels, but produced no effect on urea content, and a small reduction in ammonia content.
• 4.4. The urea concentration of the embryo was lower than in allantoic fluid.
• 5.5. It is concluded that urate production by the avian embryo is primarily concerned with the modification of allantoic fluid composition.

     

Effect of nutrition on the excretion rate of soluble nitrogenous products of Luidia clathrata (say) (Echinodermata; Asteroidea)

• 1.1. Groups of Luidia clathrata were fed maintenance level diets of Donax variabilis (50% protein by dry weight) or Penaeus duorarum (80% protein) or were starved.
• 2.2. The NH₄⁺ excretion rates for all treatments increased from 6.06 ± 2.55 to 14.39 ± 4.31 μg NH₄⁺ − N/g dry wt per hr after 20 days.
• 3.3. The urea excretion rate for all treatments was 1.25 ± 3.39 μg urea-N/g dry wt per hr for 56 days.
• 4.4. The pyloric caecum index (percentage of wet body weight) decreased 16.5 and 73.4%, for Donax variabilis-fed and starved sea stars, respectively. The pyloric caecum index of Penaeus duorarum-fed sea stars increased 81.5%. The protein level of the pyloric caeca was 47.00 ± 4.14% of the dry weight for the fed animals and 37% for the starved animals.
• 5.5. Increased NH₄⁺ excretion rates with starvation or presumed maintenance diets appear to be due to tissue catabolism.

     

Nitrogen excretion of Crassostrea virginica

• 1.Water in which groups of 6 oyster, Crassostrea virginica, had been held for 24 hr was analyazzed by standards methods for nitrogenous excretion products.
• 2.Results of the most complete analysis, expressed as μmoles ammonia/100g oyster/day, were: ammonia 12·50, urea 2·2.54, amino acids 1·01, unidentified 3·20, total 19·25.

     

Electrolyte changes,cell volume regulation and hormonal influences during acclimation of rainbow trout (Salmo gairdnerii) to salt water

• 1.1. Rainbow trout were acclimated to salt water (1.5, 2.0 or 3.0%, which means 40, 60 or 85% concentrated sea-water) and the electrolyte, glucose and cortisol concentrations of the plasma as well as the extra- and intracellular muscle space, the muscle electrolyte concentrations and the ATPase activity were analysed.
• 2.2. Plasma osmolality, Na⁺, Ca²⁺ and Mg²⁺ concentrations of the plasma had a maximum at 24 hr after the start of acclimation when acclimated to 3.0% salt water. Plasma osmolality, Na⁺ and Mg²⁺ concentrations were significantly higher during the whole acclimation time when exposed to 3.0% salt water.
• 3.3. Variations and regulations of ECS and ICS were clearly demonstrated. The intracellular electrolyte concentrations were also maximal at 24 hr.
• 4.4. The plasma glucose level was just slightly elevated, but the cortisol level clearly indicated a stress response at 24 hr.
• 5.5. The activity of gill Na-K-ATPase increased during the acclimation time.
• 6.6. The regulatory processes in trout during acclimation to salt water are compared with those occurring in tilapia and carp.

     

Sulphate conjugation is the main route of pentachlorophenol metabolism in Daphnia magna

• 1.1. Daphnia magna were exposed for 24 hr to ¹⁴C-labelled pentachlorophenol (PCP) at an initial concentration of 20μg/l in the incubation water. Occurrence of free PCP and its metabolites were measured both from the animals and the water.
• 2.2. Hydrophilic metabolites excreted into water were analysed, after acid or enzymatic hydrolyses, with a liquid-liquid extraction and TLC.
• 3.3. PCP was metabolized and excreted, perhaps solely, via the sulphate conjugation. The average excretion rate, 2.65nmol/g/hr, accounted for 35% of the absorption rate measured at the start of exposure.
• 4.4. Neonate daphnids had an equal ability to metabolize PCP as the older animals. Bioconcentration in young animals was, however, only 23% of that in adult ones.
• 5.5. Effect of naturally humic water on metabolization and excretion of PCP was negligible.

     

Heat production of fish: A literature review

• 1.1. Results of investigations on direct calorimetry and simultaneous measurements of oxygen consumption and carbon dioxide and ammonia production of fish are summarized.
• 2.2. By means of indirect calorimetric formulae, the heat production and the protein, carbohydrate and fat oxidation are calculated from the oxygen consumption and carbon dioxide and ammonia production.
• 3.3. The lowest heat production values are obtained by long-term monitoring of groups of fish during darkness and under fasting conditions.
• 4.4. It is concluded that the heat production of standard metabolism at 20°C is 700J/hr/MW (MW = metabolic weight, kg^0.85).

     

Some effects of dehydration on internal distributions of water and solutes in Xenopus laevis

• 1.1. In relation to body weight changes resulting from evaporative water losses of up to 37% of initial body weight:
  • 1.1.(a) Plasma chloride and potassium concentrations increased in proportion to total body water losses.
  • 1.2.(b) Plasma urea concentrations increased at greater rates than expected from the sum of basal synthesis and dehydration.
  • 1.3.(c) Plasma sodium concentrations initially increased less rapidly than expected from total body water losses, but by losses of 30% of initial body weight closely approximated predicted concentrations.
  • 1.4.(d) Plasma volumes decreased slightly faster than expected, while hematocrits increased as expected.
• 2.2. Skeletal muscles and the ventricular muscles of the heart retained water to greater degrees than expected. Dehydration did not elicit net shifts in Na⁺ K⁺, Cl⁻ or amino acids between the intracellular and extracellular compartments in either skeletal muscle or ventricle.

     

Light-induced transient increase of the activity of topoisomerase I in plasmodia of Physarum polycephalum

• 1.1. Activity of topoisomerase I and incorporation of [³H]uridine and [¹⁴C]thymidine were monitored during light-induced sporulation of the slime mold Physarum polycephalun.
• 2.2. A 4-fold transient increase of topoisomerase I activity but not of [³H]uridine or [¹⁴C]thymidine incorporation was observed after 42 hr of illumination with 6 hr impulses.
• 3.3. The activity of topoisomerase I did not increase in the absence of light impulses. However, ca 5-fold increase of the activity was observed in dark when 100 μ M dibutyryl-cAMP was administered 12 hr before harvesting of plasmodia.
• 4.4. Fluorodeoxyuridine and cycloheximide administered 36 hr after starting of the illumination cancelled the increase of the activity of topoisomerase I.
• 5.5. After 7 days of the illumination, when fruiting bodies appeared, the activity of topoisomerase I dropped to about 15% of the initial value.

     

Regulation of glutamine catabolism in the perfused guinea-pig liver in relation to ureogenesis and gluconeogenesis

• 1.1. L-Glutamine conversion into ammonia, urea and glucose by the perfused liver of 48 hr starved guinea-pigs was concentration dependent attaining the maximal rate at 4 mM.
• 2.2. The activity of glutaminase I (EC 3.5.12), measured in isolated liver mitochondria was high enough to account for the observed rate of ammonia, urea and glucose formation by the perfused liver. Neither NH4C1 (5 mM) nor aminooxyacetate (0.5 mM) affected the rate of glutamine conversion into glutamate by isolated liver mitochondria.
• 3.3. Gluconeogenesis and ureogenesis from glutamine was inhibited by octanoate, Dt-3-hydroxybutyrate, aminooxyacetate, ethanol and p-hydroxyphenylpyruvate while ammonia formation was stimulated by aminooxyacetate. 2,4-Dinitrophenol stimulated the rate of the formation of all three metabolites from glutamine.
• 4.4. The major changes induced by aminooxyacetate, as determined in livers perfused with glutamine and stopped by freeze-clamping technique, consisted in a decrease in the content of ATP, aspartate and malate and in a slight increase in the content of glutamate.
• 5.5. Glutamine is an effective precursor of phosphoenolpyruvate in isolated liver mitochondria. Its formation was inhibited by octanoate and by DL-3-hydroxybutyrate.
• 6.6. The data are discussed in terms of regulation of glutamine catabolism in liver with emphasis on ureogenesis and gluconeogenesis.

     

Comparative distribution of nitrogenous compounds in Acipenser transmontanus and Hydrolagus colliei: Enzyme kinetics and isozyme ratios alterations

• 1.1. Time patterns of intravenously administered [¹⁴C]urea in primitive fishes showed generalized but not quantitatively equivalent tissue distribution within defined concentration limits which were species specific (Rasmussen & Rasmussen, 1978). Comparative patterns are presented here for other ¹⁴C-labelled organics, such as thiourea, demonstrating temporal and quantitative differences in tissue distribution.
• 2.2. Demonstrable species differences between [¹⁴C]TMA and [¹⁴C]urea distribution are seen between H. colliei and A. transmontanus.
• 3.3. The tissue distribution of [¹⁴C]urea of H. colliei maintained in sea water with 0.1 M urea plus minor amounts of [¹⁴C]urea is presented; especially to be noted is the rapid distribution to the ocular fluid.
• 4.4. Finally, the effects of elevated concentrations of selected organics including urea, TMAO, guanidine-HCl on serum and CSF levels of peroxidase, lactic dehydrogenase (LDH), on some kinetic parameters of LDH, and on LDH isozyme ratios are reported. Especially enhanced by extra urea is the fastest electrophoretically migrating LDH band in ratfish CSF and serum.

     

Recycling of urea nitrogen to the gut of the tammar wallaby (Macropus eugenii)

• 1.1. The transfer of urea from plasma to the gut of tammar wallabies (Macropus eugenii) was studied using infusions of [¹⁵N]-urea and [¹⁴C]-urea in animals given either a high nitrogen chopped lucerne hay or a low nitrogen chopped oaten hay diet.
• 2.2. The proportion of urea entering the plasma pool which was degraded in the gut was similar on both diets (74–86%). Incorporation of urea into non-ammonia nitrogen in the gut was 1.1–1.7 g N/day in tammars given the high nitrogen diet, equivalent to 34–53% of dietary N intake, and 0.75–0.78 g N/day in tammars given the low nitrogen diet, equivalent to 103–112% of dietary N intake.
• 3.3. On the lucerne diet 63% of bacterial nitrogen in the midstomach was derived from ammonia.
• 4.4. It appears that blood urea is transferred into the stomach of tammars given lucerne more readily than into the rumen of sheep given lucerne.

     

Influence of temperature,rate of feeding and body weight on nitrogen metabolism of bream,Abramis brama L

• 1.1. Measurements of the rate of nitrogen consumption, total nitrogen and ammonia excretion and nitrogen absorption of bream, Abramis brama L. (body weight range 0.4–519 g wet wt) were made at 10, 15 and 20 C.
• 2.2. Fish were fed once daily on live zooplankton collected in Lake Balaton and cultured Tubifex sp. at 5–15% of their body weight.
• 3.3. Fish size and temperature had a combined effect on the rate of total nitrogen excretion. Total nitrogen excretion did not increase proportionally with an increase in consumption.
• 4.4. On average, 52–80% of the nitrogen consumed with food was excreted by bream.
• 5.5. The greatest part of total nitrogen excretion was ammonia and its proportion in the total ranged between 53 and 75%.
• 6.6. Temperature did not have any significant effect on the proportion of excreted ammonia and the rate of excreted total nitrogen was the only factor determining its proportion in the total.
• 7.7. The rate of nitrogen absorption of bream was surprisingly very high.

     

Fate of ingested leucine and glucose in the sea star,Asterias rubens,during its annual reproductive cycle

• 1.1. The distribution of radiolabel from L-leucine [¹⁴C-UL] and D-glucose [¹⁴C-UL] was measured in the sea star Asterias rubens at 1, 6 and 24 hr after oral administration.
• 2.2. Incorporation of the label from both compounds was observed in pyloric caeca, coelomocytes and ovaries even after an incubation time of 1 hr.
• 3.3. Highest incorporation from both precursors was found in proteins, while substantial radioactivity was present in the amino acids, organic acids and neutral components. Lipids were hardly labelled from leucine and only slightly from glucose.
• 4.4. Radioactivity in proteins and lipids increased with increasing incubation time. No significant differences were found in the distribution patterns of radiolabel during the reproductive cycle.
• 5.5. The data obtained are discussed in terms of current knowledge on the translocation of nutrients in echinoderms.

     

Purine metabolism in cotyledons and embryonic axes of black gram (Phaseolus mungo L.) Seedlings

• 1.1. The metabolism of purine bases and nucleosides in cotyledons and embryonic axes of black gram (Phaseolus mungo L.) was studied.
• 2.2. A large portion of absorbed [8-¹⁴C]adenine, [8-¹⁴C]guanine and [8-¹⁴C]adenosine was salvaged in nucleotide and nucleic acid synthesis.
• 3.3. Most of the radioactivity of [8-¹⁴C]hypoxanthine and [8-¹⁴C]inosine was incorporated into allantoin and allantoic acid.
• 4.4. Activity of adenine phosphoribosyltransferase in enzyme extracts was much higher than that of hypoxanthme and guanine phosphoribosyltransferase(s).
• 5.5. Apparent activity of adenosine kinase was higher than that of inosine kinase. 6. NAD⁺-dependent xan thine dehydrogenase was detected in both cotyledons and embryonic axes of the seedlings.
• 6.7. The capacity of purine salvage was higher m 24 hr old cotyledons than 24 and 48 hr old embryonic axes. The reverse was observed concerning that of purine degradation.

     

Kinetics of avidin induction by tissue injury and inflammation in chicks and the dependence of induction on protein and RNA synthesis

• 1.1. During systemic acute inflammatory reaction caused in chicks by intestinal injury or i.p. actinomycin D administration, the production of a biotin-binding egg white protein (avidin) was induced in various tissues. Local muscular burning injury induced avidin production only in the injured area.
• 2.2. Avidin production in the injured tissues was induced in 6 hr, and avidin concentrations assayed by the [¹⁴C]biotin-binding method and radioimmunoassay were maximal at 24 hr. In a few days, avidin had disappeared from the tissues.
• 3.3. Avidin induction in the injured muscle was transferred into the in vitro incubation from 4 hr after injury. Protein and RNA synthesis was needed for avidin production in vitro, and new avidin molecules were synthesized during the incubation.