K transport in upper portion of descending limbs of long-loop nephron from hamster

1987 ◽  
Vol 252 (3) ◽  
pp. F387-F392 ◽  
Author(s):  
K. Tabei ◽  
M. Imai
Keyword(s):  
Potassium Transport ◽  
Flame Photometry ◽  
Passive Permeability ◽  
A Value ◽  
Potassium Flux ◽  
Tubular Lumen ◽  
Net Flux ◽  
K Transport ◽  
Very High

By use of the in vitro microperfusion technique, we investigated potassium transport in the upper portion of the descending limb of the long-loop nephron isolated from hamster kidney. The net potassium flux determined by ultramicro-flame photometry was -0.63 +/- 1.84 pmol X mm-1 X min-1, a value that was not significantly different from zero. The salt permeability for KCl was calculated from the amount of potassium entering the tubular lumen when the concentration of potassium in the bath was increased by approximately 5 mM. The value was 38.9 +/- 1.9 X 10(-5) cm X s-1. The bidirectional fluxes of 86Rb were measured as indices of potassium fluxes. Flux coefficients from lumen-to-bath and bath-to-lumen were 51.2 +/- 9.2 and 48.8 +/- 13.5 X 10(-5) cm X s-1, respectively. These values were not significantly different, confirming that there was no net flux for 86Rb. In another series of five experiments, the lumen-to-bath 86Rb flux coefficients were 69.4 +/- 13.2 X 10(-5) cm X s-1 in the absence of unlabeled Rb, and 70.2 +/- 13.9 X 10(-5) cm X s-1 in the presence of 5 mM unlabeled Rb. The lumen-to-bath 42K flux coefficient measured in the same series of animals was 85.3 +/- 10.5 X 10(-5) cm X s-1 (n = 10), a value that is slightly higher than, but not significantly different from, that of 86Rb. These data show that active potassium transport may exist in this segment and that the passive permeability for potassium is very high.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Analysis of the coefficient of variation in shear and tensile bond strength tests

2005 ◽  
Vol 13 (3) ◽  
pp. 243-246 ◽  
Author(s):  
Fábio Lourenço Romano ◽  
Gláucia Maria Bovi Ambrosano ◽  
Maria Beatriz Borges de Araújo Magnani ◽  
Darcy Flávio Nouer
Keyword(s):  
Coefficient Of Variation ◽  
Mean Value ◽  
Scientific Article ◽  
A Value ◽  
Statistical Analysis System ◽  
Strength Tests ◽  
Analysis System ◽  
Very High

The coefficient of variation is a dispersion measurement that does not depend on the unit scales, thus allowing the comparison of experimental results involving different variables. Its calculation is crucial for the adhesive experiments performed in laboratories because both precision and reliability can be verified. The aim of this study was to evaluate and to suggest a classification of the coefficient variation (CV) for in vitro experiments on shear and tensile strengths. The experiments were performed in laboratory by fifty international and national studies on adhesion materials. Statistical data allowing the estimation of the coefficient of variation was gathered from each scientific article since none of them had such a measurement previously calculated. Excel worksheet was used for organizing the data while the sample normality was tested by using Shapiro Wilk tests (alpha = 0.05) and the Statistical Analysis System software (SAS). A mean value of 6.11 (SD = 1.83) for the coefficient of variation was found by the data analysis and the data had a normal distribution (p>0.05). A range classification was proposed for the coefficient of variation from such data, that is, it should be considered low for a value lesser than 2.44; intermediate for a value between 2.44 and 7.94, high for a value between 7.94 and 9.78, and finally, very high for a value greater than 9.78. Such classification can be used as a guide for experiments on adhesion materials, thus making the planning easier as well as revealing precision and validity concerning the data.

scholarly journals Further analysis of transcytosis of free polypeptides and polypeptide-coated nanobeads in rabbit nasal mucosa

2001 ◽  
Vol 91 (1) ◽  
pp. 211-217 ◽  
Author(s):  
Dario Cremaschi ◽  
Silvia Dossena ◽  
Cristina Porta ◽  
Vilma Rossi ◽  
Mario Pinza
Keyword(s):  
Nasal Mucosa ◽  
M Cells ◽  
Transport Capacity ◽  
A Value ◽  
Suspension Viscosity ◽  
Bead Diameter ◽  
Net Flux ◽  
Very High

In rabbit nasal mucosa, free polypeptides and polypeptide-coated nanospheres are actively absorbed by the M cells present in specialized areas of the epithelium. Because polypeptide-coated nanosphere transport was abolished in the presence of free polypeptides, free polypeptides and polypeptide-coated nanospheres are shown here to compete. Fluxes of polypeptide-coated nanospheres with 356, 490, and 548 nm diameters have been compared. BSA-coated beads were poorly transported, at the same rate, when bead diameters were 356 or 490 nm [net flux of ∼2–2.5 × 106 nanospheres (nan) · cm−2 · h−1]; however, their net transport largely increased toward a value of 25 × 106nan · cm−2 · h−1 at a diameter of 548 nm. Insulin-coated beads displayed a net flux that was significantly higher than BSA-coated beads but equally were transported at the same rate (net flux of ∼8.0 × 106nan · cm−2 · h−1) at diameters of 356 or 490 nm; once again, their net flux significantly increased toward a value of 25 × 106nan · cm−2 · h−1, if the bead diameter was 548 nm. Insulin plus anti-insulin IgG-coated 490-nm-diameter beads displayed a very high net flux, although not yet saturating (∼60 × 106nan · cm−2 · h−1); however, a significantly lower saturated net flux (once again ∼25 × 106nan · cm−2 · h−1) was shown with 548-nm-diameter beads. In conclusion, 1) in the range of 356–490 nm diameter, net transport was independent of bead diameter and, conversely, largely dependent on the coating polypeptides, and 2) at 548 nm diameter, nanospheres tended to be transferred at similar rates independently of coating kind and the maximal net transport capacity of the mucosa was reduced. The suspension viscosity largely increased with 548-nm polypeptide-coated nanospheres; this fact is hypothetically proposed to be the cause of these events.

Frusemide-Sensitive Sodium and Potassium Transport by Human Leucocytes

1985 ◽  
Vol 68 (1) ◽  
pp. 89-91 ◽  
Author(s):  
Valerie E. Johnson ◽  
P. J. Hilton
Keyword(s):  
Potassium Transport ◽  
Sodium Influx ◽  
Potassium Efflux ◽  
Sodium Potassium ◽  
External Potassium ◽  
Normal Human ◽  
Potassium Influx ◽  
Net Flux ◽  
Sodium And Potassium

1. Frusemide-sensitive sodium and potassium transport by normal human leucocytes has been studied in vitro by both isotopic and net flux techniques. 2. In physiological media the leucocyte exhibits a frusemide-sensitive influx of sodium and potassium of equal magnitude compatible with a 1:1 co-transport system. 3. Cells exposed to zero external sodium and potassium (osmolality maintained with choline) demonstrated a frusemide-sensitive sodium and potassium efflux. 4. Frusemide-sensitive potassium influx was dependent on the presence of external sodium but frusemide-sensitive sodium influx persisted unchanged in the absence of external potassium. 5. Frusemide-sensitive potassium influx was dependent on external chloride but frusemide-sensitive sodium influx was chloride-independent. 6. These last two observations make it likely that the frusemide-sensitive pathway is capable of operating in modes other than sodium-potassium co-transport.

scholarly journals Potassium and Rubidium Uptake in Freshwater Bivalves

1990 ◽  
Vol 150 (1) ◽  
pp. 395-405 ◽  
Author(s):  
T. H. DIETZ ◽  
R. A. BYRNE
Keyword(s):  
Potassium Salt ◽  
Potassium Transport ◽  
K Uptake ◽  
Rubidium Uptake ◽  
A Value ◽  
Saturation Kinetics ◽  
Salt Depletion ◽  
Net Flux ◽  
Freshwater Bivalves ◽  
Rubidium Transport

Potassium transport characteristics were investigated in three species of freshwater bivalves: a corbiculid, Corbiculafluminea, and two unionids, Carunculina texasensis and Ligumia subrostrata. Using 42K, all three were found to take up potassium from dilute artificial pondwater ([K+] about 0.05 mmoll+1). The influx (Ji) was 0.72μequiv g−1dry tissue h−1 in the corbiculid, significantly higher than the value of about 0.40μequiv g−1dry tissuer g−1 in the unionids. The K+ uptake displayed saturation kinetics in the range 0.05-0.36 mmoll−1: in Co. fluminea, there was a Jmax of 3.56μequiv g−1 dry tissue h−1 and the affinity coefficient (Km) was 0.27mmoll−1; in Ca. texasensis, Jmax had a value of 1.8 μequiv g−1dry tissue h−1 and Km was 0.16mmoll−1. Using K+-free artificial pondwater containing 0.03-0.04 mmoll−1 Rb+, the Rb+ influx was 0.41μequiv g−1 dry tissue h−1 in the corbiculid and 0.28 μequiv g−1 dry tissue h−1 in Ca. texasensis. All animals lost K+ during the rubidium flux studies, and since they contained no Rb+, the Rb+ efflux was zero and the net flux was equal to the influx. The Jmax values for Rb+ were lower than the corresponding values for potassium: in Co. fluminea, Jmax was 1.4μequiv g−1 dry tissueh+1, significantly higher than in Ca. texasensis, which had Jmax of 0.84μequiv g−1 dry tissue h−1. The rubidium Km (approx. 0.05 mmoll−1) values were significantly lower than corresponding values for potassium. Salt depletion increased the rubidium transport rate fourfold for both Co. fluminea and Ca. texasensis. High rates of net K+ uptake may account for the bivalves' inability to tolerate elevated environmental potassium.

Role of active potassium transport by integumentary epithelium in secretion of larval-pupal moulting fluid during silkmoth development

1975 ◽  
Vol 62 (2) ◽  
pp. 357-366
Author(s):  
A. M. Jungreis ◽  
W. R. Harvey
Keyword(s):  
Short Circuit ◽  
Flux Ratio ◽  
Short Circuit Current ◽  
Potassium Transport ◽  
Open Circuit ◽  
Ratio Test ◽  
Potassium Flux

1. The exuvial side of the pharate pupal integument is usually positive to the haemolymph-side, both in vivo and in vitro, during the period when the moulting fluid is being secreted. 2. The ratio of potassium flux toward the exuvial space is higher than that toward the haemolymph, under both open-circuit conditions and short-circuit conditions, demonstrating by the Flux Ratio test that potassium is actively transported across the isolated integument during this secretion period. 3. Just prior to ecdysis, while moulting fluid is being reabsorbed, the potassium flux ratios become unity, suggesting that active potassium transport has ceased, but the short-circuit current that remains suggests that some other ion is actively transported at this time. 4. We argue that the potassium salt solution, formed in the exuvial space (as water presumably follows the actively transported potassium), has three functions (1) to accomplish the gel--sol transformation, (2) to activate the gel enzymes and (3) to buffer the enzyme solution at a pH favourable to the activity of the gel enzymes.

scholarly journals Cation Regulation in the Smooth Muscle of Frog Stomach

1967 ◽  
Vol 50 (6) ◽  
pp. 1517-1546 ◽  
Author(s):  
Elizabeth W. Stephenson
Keyword(s):  
Smooth Muscle ◽  
High Rate ◽  
Stomach Muscle ◽  
Cation Composition ◽  
Wide Range ◽  
Frog Stomach ◽  
Net Flux ◽  
Net Fluxes ◽  
Very High

Cation composition of frog smooth muscle cells was investigated. Fresh stomach muscle rings resembled skeletal muscle, but marked Na gain and K loss followed immersion. Mean Na (49.8–79.7 mM/kg tissue) and K (61.8–80.1 mM/kg tissue) varied between batches, but were stable for long periods in vitro. Exchange of 6–30 mM Na/kg tissue with 22Na was extremely slow and distinct. Extracellular water was estimated from sucrose-14C uptake. Calculated exchangeable intracellular Na was 9 mM/kg cell water, and varied little. Thus steady-state transmembrane cation gradients appeared to be steep. K-free solution had only slight effects. Ouabain (10-4 M) caused marked Na gain and reciprocal K loss; at 30°C, Na and K varied linearly with time over a wide range of contents, indicating constant net fluxes. Net fluxes decreased with temperature decrease. 22Na exchange in ouabain-treated tissue at 20–30°C was rapid and difficult to analyze. The best minimum estimates of unidirectional Na fluxes at 30°C were 10–12 times the constant net flux; constant pump efflux may explain these findings. The rapidity of Na exchange may not reflect very high permeability, but it does require a high rate of transport work.

Daunorubicin and Platelet Function

1981 ◽  
Vol 45 (01) ◽  
pp. 038-042 ◽  
Author(s):  
M E Pogliani ◽  
R Fantasia ◽  
G Lambertenghi-Deliliers ◽  
E Cofrancesco
Keyword(s):  
Electron Microscope ◽  
Cellular Membrane ◽  
Hemorrhagic Diathesis ◽  
Clot Retraction ◽  
Freezing And Thawing ◽  
Platelet Factor ◽  
High Doses ◽  
Very High ◽  
Platelet Functions

SummaryThe influence of Daunorubicin on some platelet functions in vitro was investigated, using different concentrations of the drug (0.01-0.02-0.04 μg/ml). Daunorubicin was shown to inhibit Collagen and Thrombin induced platelet aggregation and the intensity of inhibition depended on both drug concentration and the time of preincubation.Daunorubicin was also shown to inhibit the release reaction, the platelet prostaglandin pathway and the availability platelet factor 3; the drug at concentrations for clinical use does not damage the platelet membrane, as is the case with the freezing and thawing test, in platelet uptake of 14C-serotonin and as confirmed by the electron microscope. When very high doses (0.16 mg) of Daunorubicin are used, lysis of the platelets can be observed and this is confirmed under the electron microscope by the presence of empty platelets with fractures at the level of the cytoplasmic membrane.Finally, Daunorubicin causes irreversible inhibition of reptilase clot-retraction, even if this is less severe than with Vincristine. Working with gel-filtered platelets, it would appear that the inhibition exercised by the drug on platelet reactions is not caused through modifications in Ca++ metabolism.The authors suggest that Daunorubicin, at the dosages used clinically, induces in vitro thrombocytopathy without damaging the cellular membrane as confirmed by the electron microscope.This impairment of platelet functions could play a part in hemorrhagic diathesis observed during Daunorubicin therapy.

Effects of Heparin Oligosaccharides with High Affinity for Antithrombin III in Experimental Venous Thrombosis

1982 ◽  
Vol 47 (03) ◽  
pp. 244-248 ◽  
Author(s):  
D P Thomas ◽  
Rosemary E Merton ◽  
T W Barrowcliffe ◽  
L Thunberg ◽  
U Lindahl
Keyword(s):  
Antithrombin Iii ◽  
Specific Activity ◽  
High Specific Activity ◽  
Factor Xa ◽  
Blood Levels ◽  
Thrombin Time ◽  
High Affinity ◽  
Very High

SummaryThe in vitro and in vivo characteristics of two oligosaccharide heparin fragments have been compared to those of unfractionated mucosal heparin. A decasaccharide fragment had essentially no activity by APTT or calcium thrombin time assays in vitro, but possessed very high specific activity by anti-Factor Xa assays. When injected into rabbits at doses of up to 80 ¼g/kg, this fragment was relatively ineffective in impairing stasis thrombosis despite producing high blood levels by anti-Xa assays. A 16-18 monosaccharide fragment had even higher specific activity (almost 2000 iu/mg) by chromogenic substrate anti-Xa assay, with minimal activity by APTT. When injected in vivo, this fragment gave low blood levels by APTT, very high anti-Xa levels, and was more effective in preventing thrombosis than the decasaccharide fragment. However, in comparison with unfractionated heparin, the 16-18 monosaccharide fragment was only partially effective in preventing thrombosis, despite producing much higher blood levels by anti-Xa assays.It is concluded that the high-affinity binding of a heparin fragment to antithrombin III does not by itself impair venous thrombogenesis, and that the anti-Factor Xa activity of heparin is only a partial expression of its therapeutic potential.

Controlled Release of Metformin Hydrochloride I. In vitro Release from Physical Mixture Containing Xanthan Gum as Hydrophilic Rate Retarding Polymer

1970 ◽  
Vol 4 (1) ◽  
Author(s):  
Mashkura Ashrafi ◽  
Jakir Ahmed Chowdhury ◽  
Md Selim Reza
Keyword(s):  
Controlled Release ◽  
Xanthan Gum ◽  
In Vitro Release ◽  
Correlation Coefficients ◽  
High Ratio ◽  
Water Soluble ◽  
Metformin Hydrochloride ◽  
Model Drug ◽  
Very High

Capsules of different formulations were prepared by using a hydrophilic polymer, xanthan gum and a filler Ludipress. Metformin hydrochloride, which is an anti-diabetic agent, was used as a model drug here with the aim to formulate sustained release capsules. In the first 6 formulations, metformin hydrochloride and xanthan gum were used in different ratio. Later, Ludipress was added to the formulations in a percentage of 8% to 41%. The total procedure was carried out by physical mixing of the ingredients and filling in capsule shells of size ‘1’. As metformin hydrochloride is a highly water soluble drug, the dissolution test was done in 250 ml distilled water in a thermal shaker (Memmert) with a shaking speed of 50 rpm at 370C &plusmn 0.50C for 6 hours. After the dissolution, the data were treated with different kinetic models. The results found from the graphs and data show that the formulations follow the Higuchian release pattern as they showed correlation coefficients greater than 0.99 and the sustaining effect of the formulations was very high when the xanthan gum was used in a very high ratio with the drug. It was also investigated that the Ludipress extended the sustaining effect of the formulation to some extent. But after a certain period, Ludipress did not show any significant effect as the pores made by the xanthan gum network were already blocked. It is found here that when the metformin hydrochloride and the xanthan gum ratio was 1:1, showed a high percentage of drug release, i.e. 91.80% of drug was released after 6 hours. But With a xanthan gum and metformin hydrochloride ratio of 6:1, a very slow release of the drug was obtained. Only 66.68% of the drug was released after 6 hours. The percent loading in this case was 14%. Again, when Ludipress was used in high ratio, it was found to retard the release rate more prominently. Key words: Metformin Hydrochloride, Xanthan Gum, Controlled release capsule Dhaka Univ. J. Pharm. Sci. Vol.4(1) 2005 The full text is of this article is available at the Dhaka Univ. J. Pharm. Sci. website

scholarly journals High Glycogen Levels in Brains of Rats with Minimal Environmental Stimuli: Implications for Metabolic Contributions of Working Astrocytes

2002 ◽  
Vol 22 (12) ◽  
pp. 1476-1489 ◽  
Author(s):  
Nancy F. Cruz ◽  
Gerald A. Dienel
Keyword(s):  
Rat Brain ◽  
Sensory Stimulation ◽  
Enzyme Inactivation ◽  
Biologically Active ◽  
Metabolic Labeling ◽  
Tissue Sampling ◽  
Normal Rat ◽  
Sampling Procedures ◽  
Very High

The concentration of glycogen, the major brain energy reserve localized mainly in astrocytes, is generally reported as about 2 or 3 μmol/g, but sometimes as high as 3.9 to 8 μmol/g, in normal rat brain. The authors found high but very different glycogen levels in two recent studies in which glycogen was determined by the routine amyloglucosidase procedure in 0.03N HCl digests either of frozen powders (4.8 to 6 μmol/g) or of ethanol-insoluble fractions (8 to 12 μmol/g). To evaluate the basis for these discrepant results, glycogen was assayed in parallel extracts of the same samples. Glycogen levels in ethanol extracts were twice those in 0.03N HCl digests, suggesting incomplete enzyme inactivation even with very careful thawing. The very high glycogen levels were biologically active and responsive to physiologic and pharmacological challenge. Glycogen levels fell after brief sensory stimulation, and metabolic labeling indicated its turnover under resting conditions. About 95% of the glycogen was degraded under in vitro ischemic conditions, and its “carbon equivalents” recovered mainly as glc, glc-P, and lactate. Resting glycogen stores were reduced by about 50% by chronic inhibition of nitric oxide synthase. Because neurotransmitters are known to stimulate glycogenolysis, stress or sensory activation due to animal handling and tissue-sampling procedures may stimulate glycogenolysis during an experiment, and glycogen lability during tissue sampling and extraction can further reduce glycogen levels. The very high glycogen levels in normal rat brain suggest an unrecognized role for astrocytic energy metabolism during brain activation.

Sign in / Sign up

Export Citation Format

Share Document