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1.
  • 1.1. Simultaneous measurement of calcium fluxes in brown trout, at low external [Ca] (20 μ mol 1−1), provided evidence of active uptake of Ca from the medium.
  • 2.2. At pH 4.5, calcium influx was inhibited and efflux was stimulated.
  • 3.3. Cd and Mn, but not Al, at concentrations within the ranges found in acid waters experiencing fish population decline, inhibited calcium influx. Efflux was unaffected.
  • 4.4. Cd and Mn stimulated sodium influx and efflux.
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2.
  • 1.1. Unidirectional Na+ influx in lamprey red blood cells was determined using 22Na as a tracer.
  • 2.2. Total Na+ uptake and amiloride-inhibitable Na+ influx increased in a saturable fashion as a function of external Na+ concentration (Nae).
  • 3.3. At 141 mM Nae, the average value of net Na+ influx was 13 ± 1.1 and the amiloride-sensitive Na+ influx was 5.3±1.1 mmol/l cells per hr (±SE).
  • 4.4. The amiloride-sensitive component of Na+ influx was significantly activated by 10−5 M isoproterenol, by 2 × 10−5 M DNP, and by cell shrinkage.
  • 5.5. Furosemide (1 mM) had no effect on the Na+ transport in red cells.
  • 6.6. The residual amiloride-insensitive component of Na+ transport was a linear function of Nae in the range of 5–141 mM. This transport seems to be accounted for by simple diffusion.
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3.
  • 1.1. Water efflux and urine production rates were measured in blue crabs acclimated to several salinities.
  • 2.2. In 100% seawater the mean rate of water efflux (31.3 ml/100g hr−1) was significantly greater than that in 50% seawater (18.9 ml/100 g hr−1.
  • 3.3. Water efflux was directly related to body weight.
  • 4.4. The mean urine production rate was significantly greater in crabs acclimated to 50% and 30% seawater (0.17 and 0.18 ml/100g hr−1) than in animals conditioned to 100% seawater (0.09 ml/100 g hr−1).
  • 5.5. The difference between theoretical net water fluxes for crabs exposed to 100% seawater and 50% seawater was similar to the difference in urine output in the same salinities, demonstrating the importance of the antennal gland in volume regulation.
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4.
  • 1.1. Twenty-eight peptides were isolated from the egg jelly of sea urchins, Tripneustes gratilla, Pseudoboletia maculata, Strongylocentrotus nudus, Echinometra mathaei (type A and B) and Heterocentrotus mammillatus and their amino acid sequences were determined.
  • 2.2. Two of the peptides obtained from T. gratilla egg jelly possessed a bromophenylalanine (Br-Phe) residue in their sequences (Gly-(Br-Phe)-Asn-Leu-Asn-Gly-Gly-Gly-Val-Gly and Gly-(Br-Phe)-Asp-Leu-Asn-Gly-Gly-Gly-Val-Gly).
  • 3.3. All of the peptides elevated cyclic GMP concentrations in the spermatozoa of the respective sea urchin and caused a shift in the apparent mol. wt of a major sperm protein of the respective sea urchin.
  • 4.4. They stimulated respiration rates of the spermatozoa of Hemicentrotus pulcherrimus as well as their own species.
  • 5.5. One-half maximal concentrations of the peptides for respiratory stimulation of H. pulcherrimus spermatozoa were between 10−11 M and 10−9 M except a methionine-containing peptide which was about 10−7 M.
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5.
  • 1.1. Freshwater gammarids from 900–1400 m depths lose Na at 1 atm, 4°C, while related shallow water gammarids are near neutral Na balance.
  • 2.2. Na+ influx rates are similar at 1 atm, 4°C, for abyssal and shallow water gammarids of similar weight.
  • 3.3. Na+ efflux is faster for abyssal gammarids than for comparable shallow water gammarids.
  • 4.4. Compressing abyssal gammarids to 90–140 atm increases Na+ influx rates enough to restore neutral Na balance, while in shallow water crustaceans, compression decreases Na+ influx.
  • 5.5. Na+ influx rates in Baikalian gammarids vary with the 0.55 power of weight.
  • 6.6. The equation Fma × t = 1.3 × W0.55 μEq/hr/animal applies to freshwater crustaceans over the weight range from 0.03 to 35 g.
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6.
  • 1.1. The role of the fumarate:NADH oxidoreduction in the anaerobic glycolysis of the sea mussel is examined and discussed.
  • 2.2. Fumarate reductase activity is present in submitochondrial particles especially from adductor muscle, digestive gland and mantle.
  • 3.3. The pH optimum of the enzyme complex is 7.9; the approx Km's for NADH and fumarate are 4.0 × 10−5 M and 6.3 × 10−5 M, respectively.
  • 4.4. The enzyme complex is inhibitied by amytal, antimycin, ethanol, malonate, phosphate, rotenone, and succinate, and stimulated by Mg2+.
  • 5.5. It is concluded that part of the mitochondrial respiratory chain is involved in the reduction of fumarate by NADH, comprising site 1 of the oxidative phosphorylation.
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7.
  • 1.1. Gains in the water content of the Fundulus heteroclitus follicle account for over 90% of the total wet weight increase, and consequentially most of the size increase, associated with meiotic maturation.
  • 2.2. Increases in intracellular Na+ and K+ actually exceed the accompanying increases in oocyte water, resulting in net gains in the concentration of these solutes. Changes in oocyte osmolality during maturation are mostly closely paralleled by variations in the concentration of K+.
  • 3.3. Concentrations of various free amino acids, including taurine, remain constant or decline during maturation.
  • 4.4. Taken together, these results suggest that an influx of K+, followed by osmotically-obliged water, is a primary cause of water uptake during oocyte maturation in F. heteroclitus.
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8.
  • 1.1. 3-hydroxykynureninase in human liver was present in cytosol and mitoehondria.
  • 2.2. The cytosolic enzyme and mitochondrial enzyme had the same physiological and enzymic properties.
  • 3.3. The enzyme had a mol. wt of 130,000 by gel filtration and isoelectric point of pH 5.9.
  • 4.4. The enzyme was active for 3-hydroxykynurenine and kynurenine, and its activity ratio was 15:1. The apparent Km values of the enzyme were 7.7 × 10−5M for 3-hydroxykynurenine, 1.0×10−3M for kynurenine and 2.5 × 10−6M for pyridoxal 5'-phosphate with 3-hydroxykynurenine.
  • 5.5. Some other properties of purified enzymes are described.
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9.
  • 1.1. Microelectrodes have been used to measure K+ activities and electrical potential differences between the perivitelline fluid (pvf) of the eggs of pike (Esox lucius) and surrounding water in a range of pH, calcium and aluminium concentrations.
  • 2.2. Potential differences between pvf and water are decreased by Ca2+ (10−3 M) while Al3+ (18 × 10−6 M) reverses the polarity of the potential difference.
  • 3.3. K+ activities in the pvf of eggs in 10−4M KCl + 10−5M NaCl are decreased by Ca2+(10−3 M).
  • 4.4. The results are discussed with reference to ion-exchange theory and chorion permeability.
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10.
  • 1.1. Hatching Caretta caretta may lose up to 12% of their initial hatched weight from water loss during emergence from the nest.
  • 2.2. After subsequent osmotic and excretory water loss in sea water, hatchlings will drink sea water (166 μl 100 g−1 hr−1) and return to their initial weight within 10–15 days, without feeding.
  • 3.3. There were no significant changes in plasma osmolarity or sodium levels over this period.
  • 4.4. This osmoregulatory strategy is in marked contrast to that seen in the estuarine crocodile, Crocodylus porosus.
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11.
  • 1.1. The behavioural responses of the freshwater snail Biomphalaria glabrata to chemical gradients of sugars were investigated by means of diffusion olfactometers.
  • 2.2. The snails proved very discriminating in their responses. Thus, only nine (39.1%) of the 23 sugars tested proved to be statistically significant attractants or arrestants. None proved to be statistically significant repellents.
  • 3.3. Of all the sugars tested maltose proved to be the most potent attractant or arrestant. The lower threshold of response to this sugar lies between 5 × 10−6 and 5 × 10−7M.
  • 4.4. The results are compared with those obtained for amino and carboxylic acids and their ecological relevance is discussed.
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12.
  • 1.1. The diffusional water permeability (Pd) of rabbit red blood cell (RBC) membrane has been monitored by a doping nuclear magnetic resonance (NMR) technique on control cells and following inhibition with p-chloromercuribenzene sulfonate (PCMBS).
  • 2.2. The values of Pd were around 6.3 × 10−3 cm/sec at 15°C, 7.0 × 10−3cm/sec at 20°C, 8.0 × 10−3 cm/sec at 25°C, 9.1 × 10−3 cm/sec at 30°C and10.7 × 10−3 cm/sec at 37°C.
  • 3.3. Systematic studies on the effects of PCMBS on water diffusion indicated that the maximal inhibition was reached in 15 min at 37°C with 0.5 mM PCMBS.
  • 4.4. The values of maximal inhibition were around 71–74% at all temperatures.
  • 5.5. The basal permeability to water was estimated as 1.6 × 10−3cm/sec at 15°C, 2.0 × 10−3cm/sec at 20°C, 2.4 × 10−3cm/sec at 25°C, 2.6 × 10−3cm/sec at 30°C, and 3.1× 10−3 cm/secat 37°C.
  • 6.6. The activation energy of water diffusion was around 18 kJ/mol and increased to 27 kcal/mol after incubation with PCMBS in conditions of maximal inhibition of water diffusion.
  • 7.7. The membrane polypeptide electrophoretic pattern of rabbit RBCs has been compared with its human counterpart.
  • 8.8. The rabbit membrane contained a higher amount of spectrin (bands 1 and 2), while the band 6 (glyceraldehyde-3-phosphate dehydrogenase) was markedly less intense.
  • 9.9. Considerable differences in the electrophoretic patterns of the two sources of RBC membranes appeared in the bands migrating in the band 4.5 region and in front of band 7, where some polypeptides were apparent in higher amounts in the rabbit RBC membrane.
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13.
  • 1.1. In the absence of sodium, the reabsorption rate of amino acid α-aminoisobutyric acid (AIB) by the nephridia of Sabella pavonina is reduced to 20% and the AIB accumulation in the cells is reduced to 10%. These results suggest the presence of sodium-dependant processes.
  • 2.2. The observed processes are reversible when control conditions are re-established.
  • 3.3. A minimum of 17mEq/l Na+ is required to restore the normal reabsorption rate.
  • 4.4. The addition ofamiloride (10−35 M) decreases the reabsorption rate, but to a lesser extent than the absence of sodium.
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14.
  • 1.1. In the presence of insulin, 10−5 M 3,3',5-triiodothyronine (T3) treatment for 1/2 hr decreased fatty acid synthesis 35% only in adipocytes from lean rats, whereas at 10−11 M through 10−7M T3 the obese adipocytes had nearly a 20% increase in fatty acid synthesis.
  • 2.2. A 2 hr pretreatment of adipocytes with 10−9 and 10−7 M T3 decreased insulin-stimulated fatty acid synthesis by nearly 20% in both lean and obese adipocytes.
  • 3.3. In the absence of insulin, the 2 hr pretreatment with 10−9 M T3 resulted in a 45% increase in lean adipocyte fatty acid synthesis, though the obese adipocytes required at least 10−7 M T3 for 2 hr to increase the non-insulin-stimulated fatty acid synthesis by 50%.
  • 4.4. At 10−9M T3 concentrations non-insulin-stimulated fatty acid synthesis was increased by 200% in lean adipose tissue explants, but obese adipose expiants were not significantly affected under these conditions.
  • 5.5. The addition of 10−9 M T3 plus insulin to the explant media decreased fatty acid synthesis by 35% in both the lean and obese tissues.
  • 6.6. The results also imply that the low T3 status of the obese rat may be contributory to the elevated fatty acid synthesis observed in obese adipocytes.
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15.
  • 1.l. High amino acid concentrations were found in the anterior coelomic fluid of a Polychaeta (Sabella pavonina Savigny).
  • 2.2. The concentrations being much higher in the fluid which penetrates the nephrostomia into the nephridia lumen than in the final urine indicates that the nephridia reabsorbs large amounts of amino acids.
  • 3.3. Nephridial perfusion experiments showed that an amino acid analogue (α-amino-iso-butyric acid, AIB) is transported by the nephidia.
  • 4.4. The transport took place across the nephridial wall owing to the presence of a carrier-mediated transport system and a diffusion system.
  • 5.5. For the carrier-mediated transport, the Vmax was 0.234 ± 0.025 nmol·min and the Km 3.715 ± 0.315mmol·l.
  • 6.6. AIB accumulated in the nephridial cells up to a maximum rate of 01.17 nmol·min.
  • 7.7. Intracellular accumulation stopped increasing when the Vmax for reabsorption was reached.
  • 8.8. These results indicate that the carrier-mediated transport of AIB is located at the apical membrane of the nephridial cell, and that AIB transport by simple diffusion takes place through the paracellular pathway.
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16.
  • 1.1. Nereis pharangeal visceral muscle is composed of obliquely striated fibres with low mitochondrial density and moderately developed sarcoplasmic reticulum.
  • 2.2. Isolated mitochondria and sarcoplasmic reticulum showed moderate passive calcium binding but only low ATP-promoted calcium binding which was inhibited by caffeine.
  • 3.3. Whole fibres preloaded with Ca45 showed a two compartment efflux. The slow, presumably intracellular, compartment accounted for only 10% of total Ca45 activity.
  • 4.4. Both acetylcholine and high KCl treatments stimulated calcium influx, causing contractures while calcium-free and EGTA treatments inhibited both these contractures and normal spontaneous contractions.
  • 5.5. Lanthanum inhibited normal contractility and KCl contractures. Lanthanum also inhibited Ca45 influx but was without effect on Ca45 efflux.
  • 6.6. It is concluded that there is little calcium storage capacity in these visceral muscle fibres and that normal contractions are strongly dependent upon extracellular calcium influx.
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17.
  • 1.1. American crocodiles (C. acutus) weighing less than 200 g are unable to grow when kept in 35 ppt sea water in the laboratory. Yet paradoxically there are some highly saline areas in south Florida where rapid growth occurs. It is possible that these conflicting observations can be reconciled by behavioral osmoregulation of young crocodiles.
  • 2.2. Hatching occurs during the rainy season and small crocodiles may drink from the brackish “lens” available during and after rainfall.
  • 3.3. Using a weekly regime of alternating exposure to 35 ppt (6 days) and 4 ppt (12–24 hr), it has been demonstrated that growth of small crocodiles occurs. Feeding takes place primarily when brackish water is available. Salinities as high as 18 ppt were drunk when crocodiles were dehydrated by 15–20% of initial mass.
  • 4.4. C. acutus and Alligator have a rather low rate of water efflux in sea water (0.2ml/100g-hr).
  • 5.5. Sodium influx in sea water of C. acutus is low, but higher than efflux. Thus there is no evidence yet for a significant role of the lingual salt glands in sodium excretion.
  • 6.6. The major adaptations to saline water of hatchling C. acutus are a low intake of sodium, an ability to selectively drink water of lower salinities, and to grow very rapidly (within 3–4 months) to a size much more tolerant of immersion in 35 ppt sea water.
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18.
  • 1.1. 14C-dichlorofarnesoate permeated rapidly into Haemonchus contortus (infective juveniles) and Panagrellus redivivus (mixed cultures) and was strongly bound by hydrophobic association (Ks > 10−4M).
  • 2.2. Uptake rose linearly with increases in temperature (5–38°C) and external concentration (C0; 0.07–2.15 × 10−4 M). Within 1 hr the internal concentration, C1 was >C C0.
  • 3.3. The pH of the medium (6–8) did not affect uptake.
  • 4.4. Efflux of dichlorofarnesoate was low: the half-time of release was > 18 hr.
  • 5.5. The uptake curve approximated to the expression C1/C0 = a(1 − e−bt) with a and b as constants and t in hr.
  • 6.6. These results clarify previous work on the inhibitory action of juvenile hormone on the development of nematodes.
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19.
  • 1.1. The acid phosphatase (AcPase, EC 3.1.3.2) IV from rat testicular tissue was purified to apparent homogeneity.
  • 2.2. The enzyme displays a native molecular weight of 70 kDa determined on gel permeation chromatography on a Sephadex G-100 column and 68 kDa using linear 5–20% sucrose density gradient centrifugation. The subunit molecular weight on SDS-PAGE analysis is 67 kDa, suggesting that the enzyme is a monomeric protein.
  • 3.3. The enzyme does not bind to Concanavaline A-Sepharose 4B column, indicating that it is not a glycoprotein.
  • 4.4. The rat testis AcPase IV is a metal activated enzyme in which Mg2+ is the metal activating agent with a Ka, = 0.88 × 10−3 M. The Michaelis constant for p-nitrophenylphosphate, in the presence of saturating concentrations of Mg2+ ions, is 0.23 × 10−3 M.
  • 5.5. The enzyme preferentially hydrolizes p-nitrophenylphosphate, phenylphosphate and ATP.
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20.
  • 1.1. A proteinaceous inhibitor for S-adenosyl-l-methionine (AdoMet)-dependent transmethylation reactions has been purified to apparent homogeneity from rat liver cytosolic fraction.
  • 2.2. The peptide was made up of 29 amino acid residues with a molecular weight of 2,584. Glycine accounted for 52% of the total amino acids.
  • 3.3. Employing AdoMet: protein-carboxyl O-methyltransferase (Protein methylase II) and bovine serum γ-globulin as in vitro substrate, the mode of inhibition was found to be non-competitive with Ki value of 1.9 × 10−8 M.
  • 4.4. When the inhibitor was present in the reaction mixture together with S-adenosyl-l-homocysteine (AdoHcy), which is a competitive inhibitor for AdoMet, the extent of inhibition exceeded that exerted by each individual inhibitor alone, suggesting that the sites of the inhibitors on the enzyme molecule are different.
  • 5.5. Almost a stoichiometric relationship exists between the enzyme and the inhibitor molecule, the ratio being approx one.
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