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1.
  • 1.1. Adenine nucleotide concentrations and metabolism in red blood cells (RBC)2 and RBC ghosts from psoriatic patients and healthy subjects were compared.
  • 2.2. The ATP and total adenine nucleotide levels and the adenylate energy charge (EC) were elevated in the blood from psoriatic patients.
  • 3.3. The rate of glycolytic production of ATP by intact RBC was unchanged, but the Na+, K+-ATPase activity of RBC ghosts was decreased significantly in psoriasis.
  • 4.4. Results suggest that the defect in adenine nucleotide metabolism is a systemic manifestation of psoriasis, and that the quantification of adenine nucleotides in RBC and in whole blood samples may be of pathophysiological value in psoriatic lesion.
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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. Homogenates of gills from the freshwater shrimp M. amazonicum exhibit the following ATPase activities: (i) a basal, Mg2+-dependent ATPase; (ii) an ouabain-sensitive, Na+ + K+-stimulated ATPase; (iii) an ouabain-insensitive, Na+-stimulated ATPase; and (iv) an ouabain-insensitive, K+-stimulated ATPase.
  • 2.2. K+ suppresses the Na+-stimulated ATPase activity in a mixed-type kind of inhibition, whereas Na+ does not exert any noticeable effect on the K+-stimulated ATPase activity.
  • 3.3. The Na+- and the K+-stimulated ATPase activities are totally inhibited by 5 mM ethacrynic acid in the incubation medium.
  • 4.4. The Na+- and the K+-stimulated ATPase activities are not expressions of the activation of a Ca-ATPase.
  • 5.5. The possible localization and roles of the described ATPases within the gill epithelium are briefly discussed and evaluated.
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4.
  • 1.1. Weekly injections of bovine growth hormone (bGH) increased the maximal transport rate of both Na+-dependent and Na+ -independent l-leucine transport with little effect on the affinity constants in the intestine of striped bass hybrids.
  • 2.2. The Na+-dependent and the Na+-independent transport of the non-metabolizable analog cycloleucine was also stimulated by bGH.
  • 3.3. The Na+ -dependent active transport was stimulated 2 days after the hormone treatment, while the stimulation of the Na+-independent diffusional transport was not observed until after 2 weeks of treatment.
  • 4.4. Studies of intestinal morphometry and l-leucine transport using brush border membrane vesicles suggested that bGH affects intestinal amino acid absorption initially by increasing the number of transporters per cell.
  • 5.5. This phase is followed by a general increase of the intestinal mass after long-term treatment with the hormone.
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5.
  • 1.1. Mineral balance was studied in meadow voles (Microtus pennsylvanicus) maintained in the laboratory.
  • 2.2. Urine and fecal Na+ contents of voles on low-Na+ diets were comparable to those reported for other herbivore species, but urine and fecal K levels were higher.
  • 3.3. Voles approached Na+ balance (input = output) on diets with Na+ content as low as 56 ppm.
  • 4.4. There was not a clearcut hypertrophy of the adrenal-gland zona glomerulosa in voles maintained on low-Na+ diets.
  • 5.5. Plasma K content and bone water content were higher in voles maintained on high-Na + vegetation diets, suggesting expansion of extracellular fluid volume.
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6.
  • 1.1. Activities of Na+-K+ ATPase and carbonic anhydrase were measured through the early post-embryonic development of Penaeusjaponicus. In adults, only the Na+-K+ ATPase activity was measured.
  • 2.2. ATPase activity was variable in the successive development stages. From zero in nauplii, the activity slightly increased in zoeae, and rose sharply in mysis stages 2 and 3.
  • 3.3. A further significant increase in activity was noted at the transition from late mysis to early postlarvae, concomitant with a change from the larval osmoconforming pattern of osmoregulation to the postlarval and adult hyper-hyporegulating pattern.
  • 4.4. The activity of Na+-K+ ATPase, measured in isolated cephalothorax, increased from PL3 to PL4 to its maximum value in PL5; at this stage, osmoregulatory capacity was fully efficient.
  • 5.5. In young stages of P. japonicus, the variations in Na+-K+ ATPase activity appear correlated with the development of osmoregulatory ultrastructures, and with osmoregulation and salinity tolerance.
  • 6.6. These results are discussed with regard to their ecological and physiological implications.
  • 7.7. In adults, the activity of Na+-K+ ATPase was high in gills and epipodites and no activity was detected in branchiostegites. These results are related to the ultrastructure of these organs.
  • 8.8. The activity of carbonic anhydrase did not change significantly in larval and postlarval stages.
  • 9.9. From these results, it is proposed that the effector sites of osmoregulation are located in branchiostegites, pleurae and epipodites in postlarvae, and in epipodites and mainly in gills in adults.
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7.
  • 1.1. Single skeletal muscle fibers were transferred from a normal Ringer solution to Na+ ion free solution, and vice versa, and tetanus responses were recorded immediately after the transfer.
  • 2.2. Fractional tetanus tension recorded immediately after the displacement from the Na+ ion free solution to normal Ringer solution was dependent on fiber diameter.
  • 3.3. Diffusion of Na+ ions along the transverse tubules was simulated [apparent diffusion constant was 3.11 × 10−6 (cm2/s)].
  • 4.4. Our results suggest that the electrotonic spreading of membrane potential, caused by an action potential in the transverse tubules, could release Ca2+ ions from sarcoplasmic reticulum.
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8.
  • 1.1. Ion dependence and vanadium-induced inhibition on branchial sac ATPase in five species of ascidian Phlebobranchiata (vanadium-accumulating) and Stolidobranchiata (iron-accumulating) were studied.
  • 2.2. The ATPase was obtained from the microsomal fraction, which was prepared from each ascidian branchial sac.
  • 3.3. The ATPase was dependent on Mg2+ and activated by exogenous Na+ + K+.
  • 4.4. Ouabain inhibited the ATPase activity in vitro, 10 μM to 100 μM vanadate, in vitro, suppressed the (Na+, K+)-ATPase.
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9.
  • 1.1. Kidney, oesophagus and gill Na+-K+ ATPase activity and serum Na+, K+ and Cl concentrations are evaluated in European sea bass during experimental acclimation to fresh water.
  • 2.2. Kidney and oesophagus ATPase increase in low salinity and reach a maximum in fresh water.
  • 3.3. Gill ATPase decreases during the acclimation trials and rises again to normal values after a 3-week stay in fresh water.
  • 4.4. Na+ and K+ serum concentrations decrease during the trials and increase back after a 3-week stay in fresh water.
  • 5.5. The correlations between enzymatic activities, serum ion concentrations, morphological changes and environmental salinity are discussed.
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10.
  • 1.1. Blood volume and plasma biochemical changes and feed and water consumption in response to a hemorrhage by phlebotomy of 30% of the calculated total blood volume with and without replacement of blood volume with physiological saline were determined in juvenile male Coturnix coturnix japonica.
  • 2.2. Plasma protein and osmolality decreased rapidly posthemorrhage and did not recover by 72 hr posthemorrhage.
  • 3.3. Plasma glucose, Na+ and K+ increased within Ihr postphlebotomy. Plasma Na+ returned to nonphlebotomized levels within 6 hr postphlebotomy.
  • 4.4. Saline replacement of blood volume resulted in hypervolemia within 3–5 min postphlebotomy.
  • 5.5. Phlebotomized quail receiving no saline recovered blood volume to 0 hr (nonphlebotomized) levels within l hr postphlebotomy.
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11.
12.
  • 1.1. Specific activity and kinetic characteristics of the (Na+ + K+)ATPase have been investigated in the gill epithelium of the hyper-hypoosmoregulator crab Uca minax.
  • 2.2. (Na+ +K+)ATPase activity is shown to be at least three times higher in the posterior gills.
  • 3.3. The kinetic study supports the hypothesis of the existence of two different (Na+ + K+)ATPases: the enzyme activity in the posterior gills could be involved in the transepithelial transport of Na+ while the activity of the anterior gills could be responsible for the intracellular regulation of Na+ and K+.
  • 4.4. Significant and specific changes in (Na+ +K+)ATPase activity occur upon acclimation to media of various salinities.
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13.
  • 1.1. In crayfish, light stimulation of the retinular cells induces a depolarizing receptor potential.
  • 2.2. Experiments were designed to determine the role of Na+ and Ca2+ on receptor potential during dark And light states.
  • 3.3. Depolarization depends on Na+ and Ca2+ availability to the retinular cell.
  • 4.4. Repolarization velocity and response duration depend on extracellular Ca2+ availability.
  • 5.5. Light adaptation increases receptor potential dependence on calcium and sodium ions.
  • 6.6. We analyse these results with respect to other invertebrate photoreceptors.
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14.
  • 1.1. Uptake of [14C]-labelled d-glucose, l-arabinose and d-fructose by intestinal and renal brush border and basolateral membrane vesicles was studied in the absence of Na+ .
  • 2.2. The Na+-independent d-glucose transport system in these membrane vesicles was saturable, sensitive to phloretin, stereospecific and accessible only to d-glucose and d-galactose.
  • 3.3. Na+-independent l-arabinose transport was not saturable even when its concentration was raised to 300 mM and it was insensitive to phloretin.
  • 4.4. Na+-independent d-fructose transport demonstrated saturation kinetics with only renal brush border membrane vesicles, but it was not inhibited by either phloretin or phlorizin.
  • 5.5. These studies indicated that the Na+-independent carrier-mediated d-glucose/d-galactose transport system of intestinal and renal brush border and basolateral membranes is clearly not shared by other monosaccharides.
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15.
  • 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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16.
  • 1.1. Nicotine at 10 mM, but not caffeine or theophylline, reduced by 20% the overshoot of the Na+-dependent d-glucose transport in ratjejunal brush border membrane vesicles.
  • 2.2. Since nicotine did not affect the transport of Na+, its inhibition on Na+-dependent d-glucose transport must be due to a direct effect upon the d-glucose transport system.
  • 3.3. Folate transport in these membrane vesicles was found to a be a free diffusion process at pH 7.4.
  • 4.4. Neither caffeine, theophylline nor nicotine has any effect on folate transport.
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17.
  • 1.1. Goldfish were kept in deionized water (DW), DW + Na+ (0.35 mM), DW + K+ (0.05 mM), DW + Ca2+ (2mM) and DW + Mg2+ (0.2 mM). In Ca-free environments, prolactin cells appear unaffected. Stimulated calcium-sensitive cells (pars intermedia) may elaborate a hypercalcemic factor.
  • 2.2. Fecal excretion, reduced in all groups, remains noticeable in DW + Ca2+
  • 3.3. Ionic losses, very low in all groups, are minimal in DW. Supplementation with K+ increases Na+ loss.
  • 4.4. Plasma Na+ Ca2+, and osmolarity decrease in DW, and still more in DW + K+. Ca2+' and Mg2+ partly suppress hyponatremia.
  • 5.5. In goldfish kept in DW and subsequently in DW + Ca2+, calcemia increases.
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18.
  • 1.1. The behaviour of the Na efflux towards Li+ was studied using single barnacle muscle fibres as a preparation.
  • 2.2. It is found that the Na efflux into Li+-ASW (artificial seawater) is reduced and that this effect is not fully reversed by returning back to Na+-ASW.
  • 3.3. Preinjection of 100 mM-EGTA reduces the magnitude of the fall of the Na efflux into Li+-ASW.
  • 4.4(a). The remaining Na efflux into Li+-ASW is further reduced by external application of 10−4 M-ouabain. (b) The remaining Na efflux in ouabain-poisoned fibres is reduced by replacing Nae by Li+. However, some fibres show a rise rather than a fall.
  • 5.5. Fibres loaded with NaCl (by injection) show a prompt and sustained stimulation of the Na efflux when Nae is replaced by Li+. A similar but less pronounced response is often seen with ouabain-poisoned fibres.
  • 6.6. Injection of LiCl (e.g. a 2 M-solution), causes a 20% fall in Na efflux. Subsequent replacement of Nae by Li+ fails to bring about a fall in the remaining efflux.
  • 7.7. Itis concluded that the Na efflux in these fibres consists of a Na-Na exchange diffusion component which is not mediated by the Na-K pump and that its operation is interrupted by injecting Li+. The relative size of this component is about one-fifth and not one-half of the Na efflux.
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19.
  • 1.1. The properties of Na+/K+-transporting ATPase in microsomal fractions from the nervous tissue of the grasshopper, Poekilocerus bufonius were investigated.
  • 2.2. Two components of ATPase activity are present.
  • 3.3. Inclusion of 1 mM ouabain in the incubation media reduced the activity of total and Na+/K+-ATPase by 57 and 79%, respectively.
  • 4.4. The maximum velocity (Vmax) was decreased by the addition of 1 mM ouabain, whereas the apparent Km value was not affected indicating a non-competitive type of inhibition.
  • 5.5. The calculated value of the pI50 was 6.4 (I50 = 3.98 × 10−7M) for ouabain inhibition of the enzyme showing great sensitivity to the cardiac glycoside ouabain.
  • 6.6. The present results show that the physicochemical properties of Na+/K+-transporting ATPase from the brain of P. bufonius are essentially the same as for the enzyme prepared from the excretory system of the insect which has been previously investigated.
  • 7.7. Dissimilarities were also observed between these tissues in the way that the enzyme from the brain was sensitive to ouabain inhibition with a non-competitive type rather than a ouabain-resistance and a competitive type of inhibition for the enzyme from the excretory system.
  • 8.8. These dissimilarities are probably due to different isoenzyme patterns available in the same insect.
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20.
  • 1.1. Uptake of l-leucine, l-phenylalanine, l-proline and l-lysine into brush border membrane vesicles from rats fed either a medium-chain triglyceride (MCT) or a long-chain triglyceride (LCT) diet was studied under conditions of the presence or absence of a Na+ gradient.
  • 2.2. From the results of initial rate, Na+-dependent transport in LCT feeding were lower than in feeding MCT. The Na+-independent transport did not vary in either group except for l-lysine uptake.
  • 3.3. For l-leucine, l-phenylalanine and l-proline in Na+ dependence, kinetic analysis revealed 4–6-fold smaller Vmax values in LCT group than in MCT group. l-Lysine in Na+-independent transport was 10-fold lower in LCT group than in MCT group. The Km values were not affected by feeding the LCT or MCT diet.
  • 4.4. It is clear that amino acid transport is regulated by different types of dietary fat. We consider that the alteration of transport activity is attributable to the changes in number of membrane-bound transport carriers but not to their affinity.
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