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1.
  • 1.1. Comparative studies on the possible origin of extremely high contents of vitamin D3 in some kinds of fish liver were performed.
  • 2.2. Neither photochemical formation of vitamin D3 in fish skin by solar radiation of 7-dehydrocholesterol (7-DHC) nor nonphotochemical enzymatic formation of vitamin D3 from 7-DHC in fish liver was demonstrated as the origin of vitamin D3.
  • 3.3. On the other hand, when bastard halibuts and carps were farmed from fingerlings to adults with feedstuff's containing vitamin D2 or D3, significant amounts of the vitamins were accumulated in the fish liver.
  • 4.4. The contents of vitamins D2 and D3 in bastard halibut liver increased according to the duration of farming and dose responses of the vitamins in carp liver were observed.
  • 5.5. Significant amounts of vitamins D2 and D3 in phytoplankton and vitamin D3 in Zooplankton and small fish were detected.
  • 6.6. Therefore, we have concluded that the most probable origin of vitamin D3 in fish liver is a result of food chains from plankton.
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2.
  • 1.1. A third form (D3) of cyclic nucleotide phosphodiesterase from Rhizobiumfrediiv/as detected and characterized for the first time.
  • 2.2. The enzyme could hydrolyse both cyclic AMP and cyclic GMP with apparent Km for cyclic AMP of approx. 0.2 μM.
  • 3.3. D3 cyclic nucleotide phosphodiesterase had a pH optimum of about 6.0 when hydrolysing cyclic AMP.
  • 4.4. The enzyme lost almost all its activity when heated to 60°C for 20 min.
  • 5.5. Gel filtration with Sephadex G-100 gave a mol. wt of approx. 42.5 kD for the native enzyme.
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3.
  • 1.1. The possible involvement of vitamin D3 in the calcium metabolism of the terrestrial crustacean Orchestia during the molt cycle was further investigated by measuring the effects of administration of exogenous 1,25 (OH)2D3 on three parameters of the calcium balance in two different compartments of the body.
  • 2.2. At the hemolymph level, a strong hypocalcémie effect was observed in intermolt and early premolt. Within the posterior caeca of the midgut, stimulation of calcium storage and calcium release were noticed during a short period surrounding the time of exuviation, with concomitant variations of the epithelial carbonic anhydrase activity.
  • 3.3. These results, together with other data, are discussed to determine the possible functions of vitamin D3, or related molecules, in the calcium turnover within the different compartments of the body, according to the successive stages of the molt cycle.
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4.
  • 1.1. The effects of sublethal concentrations of organic and inorganic pollutants on intracellular energy-rich phosphates in blue mussels, Mytilus edulis, were investigated by in vivo 31P-NMR.
  • 2.2. Formaldehyde (30 and 10mg/l), phenol, pyridine, mercury and cadmium gave marked reductions in phosphoarginine and, in some cases, the ATP amounts. The reduction in high-energy phosphate was accompanied by an increase in inorganic phosphate in all groups.
  • 3.3. A “phosphorus index”, the product of the ratios between phosphoarginine and inorganic phosphate, and ATP and inorganic phosphate, is suggested, which might serve as an early warning (“alarm”) parameter in environmental monitoring.
  • 4.4. Diversity in the responses to different pollutants make phosphorus compounds in M. edulis also an interesting element in a finger print parameter system designed to distinguish between pollutants in the marine environment.
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5.
  • 1.1. Responses of channel catfish (Ictalurus punctatus) swim-up fry to dietary calcium in soft (< 1 mg/1 as CaCO3) and hard (> 100 mg/1 as CaCO3) water were determined by feeding purified egg-white diets containing 0, 0.5, 1.0, or 2.0% calcium from CaCO3 for 8 weeks.
  • 2.2. Catfish fry fed the basal diet (0.03% Ca) in hard and soft water had lower whole-body ash and whole-body calcium concentrations but higher weight gain and survival than those fed calcium-supplemented diets.
  • 3.3. Fry in soft water generally had lower whole-body ash, whole-body calcium, and survival, as well as a higher incidence of spinal deformities than fry in hard water.
  • 4.4. Feeding higher levels of calcium to fry reared in soft water did not increase whole-body calcium levels or decrease spinal deformities to the levels observed for fry reared in hard water and fed supplemental calcium.
  • 5.5. These data indicate that calcium derived solely from dietary or environmental sources was not sufficient for optimum health of channel catfish fry.
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6.
  • 1.1. The contents of vitamin D3, 25-hydroxyvitamin D3 (25-OH-D3) and 7-dehydrocholesterol (7-DHC) in 22 kinds of fish liver samples were determined by a high-performance liquid chromatographic (HPLC) method.
  • 2.2. Vitamin D3 was detected in all fish liver samples, but its contents varied from 84 to 264,000 ng/g wet tissue. The liver of fish belonging to Carangidae and Scombridae contained large amounts of the vitamin and therefore we deduced that vitamin D3 levels in liver might have some relations with taxonomical positions of fishes.
  • 3.3. 25-OH-D3 was detected in 7 out of 22 kinds of fish liver samples, while 7-DHC was in 14 out of 22. The contents of the two sterols were generally much lower than those of vitamin D3 and there was no special relationship between the contents of the sterols and the vitamin.
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7.
  • 1.1. Both the post-moult, rockhopper (Eudyptes crestatus) and magellanic penguins (Spheniscus magellanicus) had significantly lower plasma total protein, albumin, urate, iron and potassium and higher alkaline phosphatase activity than pre-moult birds. In addition creatinine, conjugated bilirubin and inorganic phosphate in the magellanics; globulin, urate, calcium, alanine and aspartate transaminases in the rockhoppers were significantly decreased.
  • 2.2. There were significant differences in plasma bicarbonate, inorganic phosphate, alkaline phosphatase and iron concentrations between non-moulting adult and post-moult gentoo penguin (Pygoscelis papua) chicks.
  • 3.3. Absence or scarcity of the preferred nutrient requirement during the period preceding moulting could threaten the survival of any of the species, particularly of those of narrow dietary speciality.
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8.
  • 1.1. The calcitonin content of the ultimobranchial body (UBB) and plasma levels of calcitonin, calcium and phosphate were measured in rainbow trout (Salmo gairdnerii) following their transfer from fresh to sea water.
  • 2.2. The plasma calcium level remained unchanged throughout the experiment while the UBB calcitonin content, plasma calcitonin and plasma phosphate rose significantly during the hours immediately following transfer.
  • 3.3. The levels of all three subsequently fall so that, 8–15 days later, a new equilibrium was established with lower than control (fresh water) levels of UBB calcitonin, plasma calcitonin and plasma phosphate.
  • 4.4. It would appear, from these data, that calcitonin plays some part in the endocrine regulation of sea water transfer.
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9.
  • 1.1. The vitellogenic cycle of female tuatara was investigated by monitoring plasma levels of vitellogenin, calcium, total protein, inorganic phosphate (P1) and cholesterol.
  • 2.2. Vitellogenin was not detected in females in the non-reproductive condition, but was found perenially in plasma of reproducing females during vitellogenesis, which normally lasts about 3 years out of the 4 year ovarian cycle.
  • 3.3. No large year-to-year variations were found in the plasma constituents measured and there was no correlation between the oestradiol peak at mating and plasma levels of vitellogenin.
  • 4.4. The results provide further evidence that tuatara have an extraordinary prolonged and gradual vitellogenic cycle spanning several years for a single clutch of eggs. This type of reproductive cycle is unique among reptiles.
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10.
  • 1.1. The food consumption, energy, nitrogen, fat, ash, calcium, phosphate and magnesium balances of the Eurasian kestrel (Falco tinnunculus), and screech owl (Otus kennicotti) are compared.
  • 2.2. Eurasian kestrel sample values were significantly greater than screech owl sample values in the energy, nitrogen, calcium, phosphate and magnesium content in pellets, and calcium content in excrement. Phosphate content in excrement was significantly greater in screech owl samples than in Eurasian kestrel samples.
  • 3.3. The Eurasian kestrel ingested significantly greater amounts of calcium and phosphate, egested via excrement significantly greater amounts of ash, excreted or egested significantly greater amounts of energy, nitrogen, calcium and phosphate via excrement and pellets, and excreted significantly greater amounts of magnesium via excrement than did the screech owl. The screech owl assimilated significantly greater amounts of ash than did the Eurasian kestrel.
  • 4.4. The metabolizability coefficient averaged 48.32% for the Eurasian kestrel, and 49.62% for the screech owl.
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11.
  • 1.1. The generation of C2- and C3-deuterated l-lactate was monitored by 13C NMR in human erythrocytes exposed to d-[1-13glucose, d-[2-13C]glucose or d-te-13C]glucose and incubated in a medium prepared in D2O.
  • 2.2. The results suggested that the deuteration of the C1 of d-fructose 6-phosphate in the phosphoglucoisomerase reaction, the deuteration of the C1 of d-glyceraldehyde-3-phosphate in the sequence of reactions catalyzed by triose phosphate isomerase and aldolase and the deuteration of the C3 of pyruvate in the reaction catalyzed by pyruvate kinase were all lower than expected from equilibration with D2O.
  • 3.3. Moreover, about 40% of the molecules of pyruvate generated by glycolysis apparently underwent deuteration on their C3 during interconversion of the 2-keto acid and l-alanine in the reaction catalyzed by glutamate-pyruvate transaminase.
  • 4.4. The occurrence of the latter process was also documented in cells exposed to exogenous [3-13C]pyruvate.
  • 5.5. This methodological approach is proposed to provide a new tool to assess in intact cells the extent of back-and-forth interconversion of selected metabolic intermediates.
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12.
  • 1.1. Thirty-one male golden-mantled ground squirrels were divided into four physiological groups: low wt summer, medium wt summer, high wt summer and hibernation period. A second group of 10 females was divided into two groups: hibernation period at low Tb and hibernation period during a periodic arousal.
  • 2.2. Blood serum, pancreas and antral stomach region were collected from each animal.
  • 3.3. The serum was analysed by radioimmunoassay for pancreatic polypeptide immunoreactivity, the pancreas for pancreatic polypeptide and somatostatin immunoreactivity and the antral region of the stomach for gastrin immunoreactivity.
  • 4.4. Significant between-stage differences (P < 0.05) were found in serum pancreatic polypeptide concentration and in pancreatic somatostatin content.
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13.
  • 1.1. An alkaline p-nitrophenylphosphate phosphatase has been purified 440-fold from extracts of Hatobacterium halobium.
  • 2.2. The enzyme has an apparent molecular weight of 24,000.
  • 3.3. A Km value for p-nitrophenylphosphate of 1.12mM has been found under optimal conditions.
  • 4.4. The enzyme is selectively activated and stabilized by Mn2+.
  • 5.5. It requires high salt concentrations for stability and maximum activity.
  • 6.6. It displays an unusual restricted substrate specificity of 25 phosphate esters tested, only phosphotyrosine and casein were hydrolysed besides p-nitrophenylphosphate.
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14.
  • 1.1. A novel glycogen phosphorylase inhibitor was partially purified from crayfish hepatopancreas.
  • 2.2. The inhibitor was found only in two species of crayfish examined, and not in lobster, fresh and salt water clams, mussels or cockroaches.
  • 3.3. The inhibitor is a small protein (Mr = 23,000) which did not show proteolytic activity.
  • 4.4. Preliminary kinetic analysis of the inhibitory mechanism indicated that it bound to both glycogen and the glycogen phosphorylase protein.
  • 5.5. Inhibitor binding to glycogen resulted in a competitive inhibition pattern with respect to glycogen phosphorylase (inhibition constant of ca 10 μg/ml).
  • 6.6. The inhibitor also bound glycogen phosphorylase directly with a binding coefficient of 100 μg/ml resulting in a partially non-competitive inhibition pattern with respect to phosphate.
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15.
  • 1.1. The mechanism of action of glyburide (a sulfonylurea) on muscle has been investigated by measuring glucose uptake and glucose transporter (GLUT4) protein levels after chronic glyburide treatment.
  • 2.2. A dietary induced insulin resistant rat model (4 wk of high-fat, high-sucrose feeding) was given glyburide (2mg/kg/day) for 10 days and glucose uptake was measured in a perfused hindquarter preparation.
  • 3.3. Protein levels of the GLUT4 glucose transporter were determined by Western analysis.
  • 4.4. After 7 days of treatment, rats fed glyburide had lower blood glucose concentrations 2 hr (72 ± 5 vs 103 ± 12 mg/dl) and 24 hr (97 ± 7 vs 123 ± 7 mg/dl) after glyburide administration with no difference in serum insulin levels compared to vehicle treated animals.
  • 5.5. Glucose uptake was approx doubled in basal state (0 insulin) in response to glyburide (2.8 + 0.4 vs 1.7 ± 0.2μ mol/g per hr).
  • 6.6. Maximal insulin (100 nM) stimulated glucose uptake tended to be higher in the glyburide treated group, but did not reach statistical significance (8.0 ± 0.7 vs 7.0 ± 0.6 μmol/g per hr).
  • 7.7. Western analysis revealed no significant effect of glyburide on the GLUT4 protein level in skeletal muscle.
  • 8.8. These results suggest that glyburide alters glucose uptake through some mechanism other than alterations in the level of the GLUT4 glucose transporter protein.
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16.
  • 1.1. A thermostable orthophosphoric monoester phosphohydrolase (EC 3.1.3.1) from Thermus sp strain Rt41A has been purified 400-fold to give a specific activity of 25 U/mg at 60°C in IM diethanolamine (pH 11.1).
  • 2.2. The enzyme has a Mr of 160,000 and is trimeric.
  • 3.3. The half-life of the enzyme is 5 min at 85°C.
  • 4.4. The enzyme has a wide specificity for a number of phosphate monoesters.
  • 5.5. The Hm of the enzyme is pH dependent, so the pH optimum of the enzyme is affected by the substrate concentration.
  • 6.6. The enzyme is inhibited 50% by 20 mM Ca2+ or Mg2+.
  • 7.7. The Ki for phosphate, EDTA-di sodium salt and arsenate (in 1 M diethanolamine, pH 11.1) is approx 1.2, 1.6 and 4mM respectively.
  • 8.8. Urea (200 mM) is not inhibitory.
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17.
  • 1.1. The effect of incorporating D2O into the incubation medium on glycolysis and gluconeogenesis by hepatocytes from fasted rats was examined.
  • 2.2. The substitution by heavy water, D2O, at concentrations from 10 to 40%, stimulated glucose uptake, lactate production and CO2 yields from glucose. At 10 mM glucose, 40% D2O doubled glucose uptake, increased CO2 production by 40%, and increased lactate production by 350%.
  • 3.3. The stimulation of lactate production decreased at higher glucose concentrations, but was still substantial even at 80 mM glucose.
  • 4.4. There was no effect on CO2 production above glucose concentrations of 30 mM.
  • 5.5. Ten percent D2O showed little inhibition of lactate uptake, its oxidation and gluconeogenesis. At 40% D2O the inhibition ranged from 10 to 20%.
  • 6.6. No effect of D2O on the rate of glucokinase or glucose-6-phosphatase was observed.
  • 7.7. The concentration of fructose, 2,6-P was not affected by D2O
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18.
  • 1.1.Juvenile Japanese eels (Anguilla japonica) were fed on a diet supplemented with estradiol-17β (E2) at doses of 25, 50 and 75 mg/kg. The effects on growth, sex distribution and body composition were investigated in two groups of gonadally undifferentiated stages (early and later juvenile stages).
  • 2.2.Feminization (95–100%) was observed in all E2-treated groups.
  • 3.3.The growth rate of fish treated with 25 and 50 mg/kg E2 diet at the early juvenile stage was significantly increased.
  • 4.4.The amount of protein in muscle decreased and that of fat increased in the E2-treated groups except in the early juvenile stage fed with 25 mg/kg E2.
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19.
  • 1.1. Relative to rabbit erythrocytes, chicken red blood cells exhibit a much greater capacity to utilize [3H]adenine for nucleotide synthesis in vitro, even at 5°C and in the absence of added inorganic phosphate.
  • 2.2. This difference is largely due to a higher concentration of phosphoribosylpyrophosphate and greater activity of adenine phosphoribosyltransferase in the avian cells. lli]3. The capacity of avian erythrocytes for utilization of guanine and hypoxanthine is several fold less than that of adenine.
  • 3.4. The data are consistent with lower activity for hypoxanthine/guanine phosphoribosyltransferase than for adenine phosphoribosyltransferase in intact chicken erythrocytes.
  • 4.5. The results indicate that reutilization of adenine by chicken erythrocytes may be physiologically significant.
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20.
  • 1.1. Fundamental chitin digestion characteristics of Crassostrea virginica crystalline style were investigated.
  • 2.2. Optimum temperature and pH were 34°C and 4.8. respectively.
  • 3.3. The colloidal regenerated chitin (0.56mol/0.5 ml: GlcNAc equivalents) was saturating under all enzyme levels encountered.
  • 4.4. There was no evidence of end product inhibition, even after 100 hr incubation.
  • 5.5. Calculated Km for the chitinase complex was 1.19mM when determined using a 30 min assay, but was only 0.70 mM when determined using a 4.6 hr assay.
  • 6.6. Both Km values are lower than reported for similar assays in other molluscs and for most bacteria.
  • 7.7. Effect of substrate preparation on the kinetics are discussed.
  • 8.8. Eight peaks of chitinase activity were resolved by DEAE-Fractogel ion exchange chromatography.
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