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1.
 
  • 1.The levels of water, Na, K, Ca and Mg in blood serum, brain and kidney and aldosterone level in blood of Naja haje haje were studied during the different phases of the annual cycle.
  • 2.The water content in the tissues studied displayed only minor changes as the animals passed from one phase to the other.
  • 3.A significant increase in Na was recorded in the brain during the different phases indicating a depressed sodium pump, whereas the blood Na level showed a significant decrease during hibernation.
  • 4.K increased in blood serum, brain and kidney during hibernation, while a nonsignificant decrease was found in blood serum during arousal. The brain may act as a potassium reservoir.
  • 5.An increase in Ca and Mg concentration was recorded in blood serum, brain and kidney during prehibernation and hibernation. The data suggested a homeostatic function in the transport and metabolism of these cations.
  • 6.Aldosterone exhibited a highly significant decrease especially during hibernation. The aldosterone regulation of ionic composition is discussed.
  • 7.Na/K and Ca/Mg ratios in the brain may explain the decreased excitability during winter torpor.
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2.
  • 1.1.|Friend erythroleukemia cells (FELC, a differentiating cell line) were heated at various temperatures and heating sequences. Heat treatments which ranged from 41.0 to 45.0°C and did not cause differentiation in FELC and inhibited the differentiation response to DMSO in FELC.
  • 2.2.|Heating resulted in cell killing which increased with temperature and heating time. Protracted low temperature heating (40.0–42.0°C) or incubation at 37°C between two heat treatments at 45.0°C resulted in thermotolerance for both the endpoints of cell killing and differentiation.
  • 3.3.|High temperature heating (45.0°C) before heating at 41.0–42.0°C resulted in increased thermal sensitivity to the latter heat treatments. This was observed for both the survival and differentiation endpoints.
  • 4.4.|A comparison was made of the thermal sensitivity for the two endpoints of cell killing and differentiation.
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3.
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Highlights
  • •Proteogenomics and secretome comparison of human and zoonotic Staphylococcus aureus lineages.
  • •869 secreted proteins identified in eight S. aureus isolates of CC8, CC22 and CC398.
  • •CC398 lower secretion of surface proteins and higher secretion of hemolysins and exoenzymes.
  • •Regulatory differences in the secretomes could be linked to lower SigB activity in CC398.
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4.
  • 1.1. A complete haematological profile of the cichlid Oreochromis aureus Steindachner is presented.
  • 2.2. Inaccuracies due to anticoagulant solutions under different conditions are considered and the most accurate method for determining a complete haematological profile is discussed.
  • 3.3. O. aureus parameters appear to be similar to those of O. niloticus and O. mossambicus reported in the literature. Haemoglobin concentration is higher than in the latter two species.
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5.
  • 1.1. The taurine content of erythrocytes from 15 avian species contained levels of taurine in the range of 20–70 mmol/kg of hemoglobin, about 100-fold that of mammalian red blood cells.
  • 2.2. This high taurine content did not appear to be related to the nucleation of these cells as nucleated amphibian erythrocytes and human reticulocytes contained low levels.
  • 3.3. The erythrocytes lacked cysteine sulfinic acid decarboxylase, a key enzyme in the synthesis of taurine from cysteine, indicating a probable lack of synthetic capabilities.
  • 4.4. The cells were able to accumulate labeled taurine against a concentration gradient. This uptake was inhibited by β-alanine and was Na+-dependent.
  • 5.5. When incubated in hypotonic medium, the cell volume of pigeon erythrocytes rapidly increased and was followed by a much slower return to normal size. The cell volume reduction was accompanied by a slow efflux of taurine into the medium.
  • 6.6. These data suggest that taurine plays a role in cell volume maintenance and osmotic regulation in avian erythrocytes.
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6.
  • 1.1. Hemolymph lectins (agglutinins) of the cotton caterpillar Spodoptera littoralis were analyzed by agglutination, cross-absorption and carbohydrate-hemagglutination inhibition using several vertebrate erythrocytes.
  • 2.2. Lectins were found to interact, with all tested erythrocytes, by binding to carbohydrate moieties but showing no definite specificity.
  • 3.3. Disulphide bonds were probably absent as 2-ME treatment was ineffective.
  • 4.4. By cross-absorption studies, we have proposed that the hemolymph contains multiple lectins.
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7.
  • 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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8.
  • 1.1. The role of aldosterone on active potassium transport across lizard colon under voltage-clamped conditions has been investigated.
  • 2.2. Control colons exhibited no net potassium flux (Jknet) despite of the existence of active opposite unidi ectional fluxes.
  • 3.3. An important net secretory potassium flux was found in short-circuited aldosterone-stimulated colons.
  • 4.4. Mucosal amiloride did not change (Jknet) either in control or aldosterone-stimulated colons.
  • 5.5. Luminal barium alters K + transport in a manner consistent with the presence of barium-sensitive conductances at the apical membrane of both control and aldosterone-treated colons.
  • 6.6. The effects of ouabain and barium on control and aldosterone-induced potassium flows were consistent with a model involving basolateral uptake by an Na +-K +-ATPase and conductive exit across the apical membrane.
  • 7.7. The stimulatory effect of aldosterone on potassium secretion is associated with parallel increases of both basolateral K + entry and the apical conductive pathway.
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9.
  • 1.1. Compositions of lipids and proteins of erythrocytes (RBC) and gills from Japanese charr (Salvelinus leucomaenis) which were exposed to 0.4 and 0.7 ppm ozone for 30 min were compared with those of the control.
  • 2.2. On exposure to ozone, both RBC and gill membrane phospholipid content, especially phosphatidylethanolamine (PE), dropped.
  • 3.3. The decrease of PE was brought about by the decrease of docosahexaenoic acid content which comprised the major component of PE.
  • 4.4. RBC membrane protein with 215 and 225 kDa, which is equivalent to cytoskeletal protein, selectively disappeared on exposure to ozone.
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10.
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Highlights
  • •Interplay of epithelial cells and internalized S. aureus was dissected over 96 h.
  • •Surviving host cells contain nonreplicating bacteria that persists in the cytoplasm.
  • •Competition over resources triggers temporal metabolic changes.
  • •Metabolic adaptation of host and bacteria determines the outcome of infection.
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11.
  • 1.1. To date, only a few authors have assayed the agglutinic activity of marine algae against fish erythrocytes, and in these cases, mainly against freshwater fish.
  • 2.2. For the first time, the hemagglutinic activity of 70 seaweeds (29 brown, 37 red and four green algae) against erythrocytes of 16 seaflsh species is reported.
  • 3.3. The presence of agglutinins was demonstrated in 100% of algae assayed, against at least one of the different types of erythrocytes tested.
  • 4.4. The results obtained confirm the presence of receptors for algae agglutinins on the surface of the erythrocytes of the fish studied.
  • 5.5. This could be useful in establishing the origins of fish populations, as these serological differences could distinguish between populations of cultivated and wild fish.
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12.
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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13.
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Highlights
  • •Establishment of a flow system allowing multi-omics analysis of S. aureus biofilms.
  • •Biofilm proteome profiling (intracellular and ECM) plus metabolic footprint analysis.
  • •Virulence factors and ribosomal proteins stabilize the ECM as moonlighting proteins.
  • •They act as electrostatic bridges between anionic cell surfaces, eDNA and metabolites.
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14.
  • 1.1. An anticoagulant solution was designed from data on osmolality, ionic concentration and pH to resemble shrimp haemolymph.
  • 2.2. This Shrimp Salt Solution (SSS) prevents coagulation and prophenoloxidase system activation during the extraction of shrimp haemolymph.
  • 3.3. The location of the the proPO system in the brown shrimp (Penaeus californiensis) was determined using this anticoagulant solution.
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15.
  • 1.1. Lipid, glucose and glycogen concentrations were measured in different tissues of the crab Chasmagnathus granulata during emersion.
  • 2.2. After 6 hr of emersion no reduction in the total amount of carbohydrates was found to occur, suggesting that a general metabolic arrest was taking place.
  • 3.3. A transitory increase in haemolymphatic glucose and lipid levels was observed. Possible causes are therefore discussed in relation to changes in the flux of substrates for energy production.
  • 4.4. The mobilization of carbohydrates and lipids to the gills, observed only during summer, may be concerned with energy supplying for ionic regulation.
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16.
  • 1.1. Milk samples of 4 ml or more were obtained from guinea pigs (Cavia porcellus), dairy cattle (Bos taurus), horses (Equus caballus) and humans (Homo sapiens). The milks were analysed for minerals including calcium (Ca), phosphorus (P), magnesium (Mg), potassium (K) and sodium (Na) by Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES).
  • 2.2. Calcium was approximately twice as concentrated in guinea pig milk as in cows' milk, which was twice as much as the level in mares' milk, and this, in turn, was twice as concentrated as human milk.
  • 3.3. The ratio of Ca to P in guinea pig milk was 1.66:1, while it was 1.24:1 in cows' milk, 1.56:1 in mares' milk and 2.07:1 in human milk.
  • 4.4. Potassium was the most abundant mineral in the milks of cows, mares and humans, but not in guinea pig milk, and was much higher in cows' milk than in others.
  • 5.5. Sodium was highest in guinea pig milk with cows' milk being a close second.
  • 6.6. Magnesium was one-tenth as concentrated as Ca.
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17.
  • 1.1. The cytogenetic effects of various i.p. treatments with five carcinogenic-mutagenic chemicals and three doses for each (aflatoxin Bl, Aroclor 1254, benzidine, benzo[a]pyrene and 20-methylcholanthrene), were investigated in the cells of the common carp, Cyprinus carpio.
  • 2.2. Injection with distilled water and corn oil served as the two control groups.
  • 3.3. For detecting cytogenetic damage we used two test systems, chromosomal aberrations (CA) in kidney cells and micronucleated erythrocytes (M).
  • 4.4. At 48 hr after treatment with the chemicals under investigation, the frequencies of CA and M were clearly increased in a dose-response manner compared to the control groups.
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18.
  • 1.1. In sea-water, adult salmon (S. salar) exchange an average of 12.6% of total body sodium/hr.
  • 2.2. Following transfer to fresh water sodium uptake follows Michaelis-Menton kinetics. Fmax = 2.40 mmol Na/1 ECF/hr, Km = 0.26 mmol Na/1. The uptake system is fully activated immediately following transfer to fresh water.
  • 3.3. Post smolts adapted to sea-water for 3 months take up sodium at only one third of the rate of adult fish following return to fresh water.
  • 4.4. The concentration of prolactin in the plasma is low in sea-water adapted fish and does not rise during the first 8 hr in fresh water.
  • 5.5. At pH 5 sodium uptake is reduced by almost 90%, even in the absence of aluminium, but recovers immediately on return to neutral water.
  • 6.6. At pH 5 and 20 μmol Al/1 there is little further effect on sodium uptake but after 6 hr in aluminium the inhibition of sodium uptake continues after return to neutral aluminium fresh water and uptake is only 50% of normal 24 hr later.
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19.
In vitro influence of vanadate and vanadyl ions on the activities of Na,K- and Ca,Mg-ATPase from synaptosomal membranes of the parietal lobe of the human brain were compared.
  • 1.1. Vanadate and vanadyl inhibit the enzymes activities in the investigated fraction.
  • 2.2. Vanadate is a more effective inhibitor of both ATPases in the concentrations above 50 μM and vanadyl is an effective inhibitor in a very low concentration (10 nM).
  • 3.3. Vanadate seems to be an uncompetitive inhibitor of Na,K-ATPase (k1 = 880 nM).
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20.
  • 1.1. Sterols were identified from eight isolates of five species in the Chromophycota that were cultured axenically and harvested in the stationary phase.
  • 2.2. Analyses were performed on four strains from the Prymnesiophyceae, two strains from the Cryptophyceae and one from the Bacillariophyceae. Most strains examined contained only one major sterol, 24-methyl-22-dehydrocholesterol.
  • 3.3. Analysis by capillary GC, HPLC, and in one instance NMR, showed that the two strains provisionally identified as Isochrysis contained brassicasterol (24β-methyl-22-dehydrocholesterol); whereas, all other species examined contained primarily epibrassicasterol (24α-methyl-22-dehydrocholesterol).
  • 4.4. Stigmasterol (24α-ethyl-22-dehydrocholesterol) accompanied epibrassicasterol in Pleurochrysis carterae.
  • 5.5. Analyses of C-24 alkyl isomers in these algae may provide useful information concerning their taxonomic placement.
  • 6.6. The occurrence of both isomers of 24-methyl-22-dehydrocholesterol in oysters is explained by the occurrence of both isomers among algae which are probably dietary sources for oysters.
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