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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. Vitamin D3 (10IU and 100IU/100 g body weight) and 1,25(OH)2D3 (0.5, 5 and 50 U) were administered daily to unfed male carp Cyprinus carpio for 10 days. The serum calcium and inorganic phosphate levels were measured colorimetrically.
  • 2.2. The serum calcium level increased significantly in all treated groups; this increase is dose-dependent.
  • 3.3. The serum inorganic phosphate was elevated in the treated groups on days 3 and 5.
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3.
  • 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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4.
  • 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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5.
  • 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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6.
  • 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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7.
  • 1.1. The glyoxylic acid cycle pathway could be regulated through the modulation of the isocitrate dehydrogenase-NADP activity. This enzyme is inhibited by NADPH.
  • 2.2. The effect on the glyoxylate cycle flux of variations in the rate of the NADPH-consuming pathways has been studied.
  • 3.3. Increase in the rate of NADPH-consuming activity by addition of H2O2 produces inhibition of the glyoxylate cycle and decrease in the NADPH/NADP ratio.
  • 4.4. These results suggest that the glyoxylate flux in Tetrahymena could be modulated by regulation of NADP-dependent isocitrate dehydrogenase by the NADPH/NADP ratio.
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8.
  • 1.1. Effects of antioxidants (butylated hydroxytoluene and nor-dihydroguaiaretic acid), vitamin K-related quinones (vitamin K1 and coenzyme Q10) and inorganic copper (CuSO4), in concentrations inhibiting NADPH: cytochrome P -450 reductase, were re-examined on benzo(a)pyrene metabolism in mouse liver uninduced microsomes.
  • 2.2. It was found that all these compounds decrease production of the two-electron oxygenation products of benzo(a)pyrene (monophenoles, diols) and the amounts of glucuronides in a manner parallel to their inhibitory potency against NADPH: cytochrome P-450 reductase.
  • 3.3. No correlation was found between amounts of one-electron oxidation products of benzo(a)pyrene and inhibition of NADPH: cytochrome P-450 reductase.
  • 4.4. Without added UDPGA the compounds studied decreased protein associated benzo(a)pyrene metabolites in parallel to the decreased overall metabolism of this polyaromatic hydrocarbon.
  • 5.5. The mode of action of the studied compounds is discussed.
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9.
  • 1.1. Total chromophore contents as well as the contributions made by 11-cis retinal were determined by high pressure liquid chromatography in light- and dark-adapted eyes of Orchomene plebs and Glyptonotus antarcticus (Amphipoda and Isopoda, respectively).
  • 2.2. In O. plebs the highest amount of total chromophore in pmol/eye was found to be 18.5 in 36 hr dark-adapted animals. The lowest amount (11.6 pmol/eye) was recorded in 24 hr light-adapted individuals.
  • 3.3. In dark-adapted O. plebs, irrespective of whether dark-adapted for 36 or 60 hr, the percentage of 11-cis retinal was maximally 96.6%. In the light-adapted material it reached 71.2%
  • 4.4. In eyes of 20 hr dark-adapted Glyptonotous antarcticus, possibly because of insufficient dark adaptation, a total chromophore content of only 3.2 pmol/eye was found. The percentage of 11-cis retinal was 55.8.
  • 5.5. Porphyropsin with its testable 3-dehydroretinal (vitamin A2-aldehyde) was not encountered in any of our samples.
  • 6.6. Calculations of photopigment per gram body weight and a comparison with data from freshwater crayfish show that dark-adapted O. plebs possess approximately 20 times the relative photopigment amount of the crayfish. Absolute sensitivity of the eye of O. plebs is, therefore, expected to be very high.
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10.
  • 1.1. The total body water, lipid content, and cuticular permeability of fungus infected and uninfected German cockroaches, Blattella germanica, were examined.
  • 2.2. Infected adult cockroaches weighed less and had significantly more body water than did uninfected specimens of the same size.
  • 3.3. Uninfected medium-size nymphs weighed significantly more than infected nymphs, but there was no difference in body size between infected and uninfected small nymphs.
  • 4.4. Cuticular permeability and lipid content of infected and uninfected cockroaches was not significantly different.
  • 5.5. Sequestering of water by the fungal cells is discussed as a possible factor in the pathology of this fungal parasite.
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11.
  • 1.1. The properties of ATPase activity were studied with the cells at the early stationary phase of Saccharomycopsis fibuligera.
  • 2.2. Optimal pH for the activity was approximately 7.
  • 3.3. The activity was stimulated by Mg2+.
  • 4.4. The activity was inhibited by NaF, DCCD, oligomycin, NaN3, NaVO3, or PCMB but not inhibited by ouabain.
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12.
  • 1.1. The benefit of dietary vitamin E supplementation in preventing oxidative-induced lung injury was investigated. Three day preterm guinea pig pups were exposed to hyperoxic (85% O2) or normoxic (21% O2) conditions. The animals were fed either a standard low birthweight human infant formula milk (6.4 mg/l vitamin E), or a vitamin E supplemented milk (100 mg/l) for up to 7 days.
  • 2.2. After 3 days vitamin E supplementation, plasma but not erythrocyte vitamin E concentrations were elevated, while following 7 days both plasma and erythrocyte vitamin E concentrations were significantly increased.
  • 3.3. Lung and liver vitamin E concentrations were elevated at both 3 and 7 days. At 3 days the increase in lung vitamin E was oxygen-dependent, suggesting that the lung increases uptake of vitamin E in response to oxidative stress.
  • 4.4. Despite an increase in the vitamin E concentration of the lungs of preterm guinea pigs, no amelioration of the lung injury was observed. These results suggest that although vitamin E is a potent antioxidant, it is unable to protect adequately the lungs from reactive oxygen species in the absence of sufficient primary enzymatic antioxidant defences.
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13.
This paper comments on: Low, B. S., Alexander, R. D., and Noonan, K.M. Human hips, breast, and buttocks: Is fat deceptive? Ethology and Sociobiology 8: 249-247, 1987. In it I argue that:
  • 1.1. Sexual selection has probably not been the most important selection pressure on
  • 2.female human body shape.
  • 3.2. Male humans in different cultures find different aspects of the female body attractive
  • 4.and therefore are unlikely to have exerted consistent directional sexual selection on
  • 5.the female body.
  • 6.3. Breast size is not correlated with lactation success.
  • 7.4. Visible hip width is not correlated with parturition success.
  • 8.5. Women would lower their fitness if they tried to deceive men about their internal
  • 9.pelvic dimensions.
  • 10.6. There are many alternative hypothesis to explain the existence of fat onwomen's
  • 11.breast, hips, and buttocks.
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14.
  • 1.1. In Musca domestica haemolymph a lipid transfer particle (LTP) is present.
  • 2.2. Musca domestica LTP is able to catalyze the transfer of lipids between different housefly lipophorin forms and also between lipophorins of Diptera and Lepidoptera.
  • 3.3. The lipophorin of larval Dione juno (Lepidoptera) was purified and is composed of two apolipoproteins, apolipophorin I (Mr = 209,000) and apolipophorin II (Mr = 85,000) with a density of 1.124 g/ml.
  • 4.4. The density of housefly lipophorin undergoes variations during the gonotrophic cycle.
  • 5.5. The lipophorin density variation results suggest that when a high rate of lipid utilization occurs, the lipophorin has a higher density value.
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15.
  • 1.1. Subcellular distribution of (NA+, K+-ATPase and ouabain-insensitive ATPase (Mg2+-ATPase) are compared in branchial tissues of the euryhaline crab, Eriocheir sinensis, acclimated to fresh water.
  • 2.2. Both the anterior and posterior gills contain cAMP-dependent protein kinase and endogenous protein substrate for phosphorylation.
  • 3.3. Phosphorylation occurs in both “particulate” and “soluble” subcellular fractions but its stimulation by cAMP is restricted to the “soluble” fraction.
  • 4.4. serotonin (5-HT) and dopamine receptors are present only in the “light particulate” fraction isolated from the posterior gills.
  • 1.(a) Serotonin and dopamine have no effect on the phosphorylation observed in a subcellular fraction alone.
  • 2.(b) Activation of the phosphorylation by serotonin and dopamine is found when the soluble fraction (source of cAMP-dependent protein kinase) is added to the fraction P3 from the posterior gills.
  • 3.(c) No activation occurs with the fractions P3 as well as P1 or P2 (not shown) from anterior gills of fresh water crab.
  • 4.(d) Cyproheptadine, a serotonin receptor antagonist, inhibits the 5-HT dependent increase in phosphorylation.
  • 5.(e) The dopamine receptor antagonist, chlorpromazine, inhibits dopamine-stimulated phosphorylation.
  • 6.5. Ouabain mimics the effect of cyproheptadine on the serotonin-stimulated phosphorylation found in the posterior gills.
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16.
  • 1.1. In brush border membrane vesicles isolated from eel kidneys, adapted either to sea water or freshwater environments, a Na+/H+ antiporter is present.
  • 2.2. Using a calibration plot it is possible to evaluate the amount of protons that this antiporter can accumulate inside the vesicular space.
  • 3.3. The activity of the antiporter seems to be affected by the salinity of the water; it is higher in animals adapted to seawater.
  • 4.4. This adaptation seems to occur by a Jmax regulation of the antiporter.
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17.
  • 1.1. To characterize an enzyme which metabolizes retinal in liver microsomes, several properties of the enzymatic reaction from retinal to retinoic acid were investigated using rabbit liver microsomes.
  • 2.2. The maximum pH of the reaction in the liver microsomes was 7.6.
  • 3.3. The Km and Vmax values for all-trans, 9-cis and 13-cis-retinals were determined.
  • 4.4. The reaction proceeded in the presence of NADPH and molecular oxygen.
  • 5.5. The incorporation of one atom of molecular oxygen into retinal was confirmed by using oxygen-18, showing that the reaction comprised monooxygenation, not dehydrogenation.
  • 6.6. The monooxygenase activity was inhibited by carbon monoxide, phenylisocyanide and antiNADPH-cytochrome P-450 reductase IgG, but not by anti-cytochrome b5 IgG.
  • 7.7. The enzymatic activity inhibited by carbon monoxide was photoreversibly restored by light of a wavelength of around 450 nm.
  • 8.8. The retinal-induced spectra of liver microsomes with three isomeric retinals were type I spectra.
  • 9.9. The microsomal monooxygenase activity induced by phenobarbital or ethanol were more effective than that by 3-methylcholanthrene, clotrimazole or β-naphthoflavone.
  • 10.10. These results showed that the monooxygenase reaction from retinal to retinoic acid in liver microsomes is catalyzed by a cytochrome P-450-linked monooxygenase system.
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18.
  • 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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19.
  • 1.1. A new tetralysine endopeptidase from Escherichia coli AJ005 has been purified about 135-fold.
  • 2.2. The peptidase seems to be specific to tetralysine among lysine homopolymers.
  • 3.3. The optimal pH was about 7.5
  • 4.4. The activity was inhibited by KCN but not inhibited by soybean trypsin inhibitor.
  • 5.5. The apparent Km value was 2.5 × 1O−3 M for tetralysine.
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20.
  • 1.1. When blood flows, membranes are bombarded with ions etc., whose entry creates an ATP demand proportional to flow rate. Also proportional to flow rate is ATP production from oxidation of substrates [S] from the same blood volume.
  • 2.2. O2 is limiting and reaction velocity at rest (metabolic rate) is determined by flow rate, F, but not by [S].
  • 3.3. Since resting blood O2 A-V difference is about 5 vol%, 11 circulated produces about 0.25 kcal in mammals, birds or warm reptiles.
  • 4.4. Where O2 is not limiting, as in most amino acid deaminations, V = K F[S] with K a constant unrelated to Km.
  • 5.5. At equal blood vol/kg, solid geometry dictates that the average cross-sectional area of major vessels/kg will be an inverse function of body mass. The smaller the animal, the shorter the vessels, the “thicker” the vessels/kg body wt, and at any one blood pressure, the higher the flow/kg/hr. If a man's major vessels were equal in cross-section/kg to those of a shrew, it would take 2241 of blood to fill them.
  • 6.6. Growth decreases flow/kg (and therefore metabolic rate), by decreasing vessel cross-section/kg without changing blood pressure or linear velocity of flow.
  • 7.7. Surface area/g, body wt to some power, average vessel length/kg, circulation time and average major vessel cross-sectional area are all related mathematically.
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