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  • Urate  (4)
  • Nierentubulus  (3)
  • Proximal tubule  (2)
  • 1
    ISSN: 1432-2013
    Keywords: Ouabain ; Frog kidney ; Proximal tubule ; Ion sensitive microelectrodes ; Na+/K+ pump ; Intracellular K+, Na+, Cl−, pH, Ca2+
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Using conventional and ion selective microelectrodes, the effect of ouabain (10−4 mol/l) on peritubular cell membrane potential (PDpt), on intracellular pH (pHi) as well as on the intracellular ion activities of Cl− (Cl i − ), K+ (K i + ), Na+ (Na i + ) and Ca2+ (Ca i 2+ ) was studied in proximal tubules of the isolated perfused frog kidney. In the absence of ouabain (PDpt=−57.0±1.9 mV), the electrochemical potential difference of chloride (apparent {ie6-1} and of potassium {ie6-2} is directed from cell to bath, of H+ {ie6-3}, of Na+ {ie6-4} and of Ca2+ {ie6-5} from bath to cell. Ouabain leads to a gradual decline of PDpt, which is reduced to half (PDpt, 1/2) within 31±4.6 min (in presence of luminal glucose and phenylalanine), and to a decline of the absolute values of apparent {ie6-6}, of {ie6-7}, {ie6-8} and {ie6-9}. In contrast, an increase of {ei6-10} is observed. At PDpt, 1/2 apparent Cl i − increases by 6.2±1.0 mmol/l, pHi by 0.13±0.03, Ca i 2+ by 185±21 nmol/l, and Na i + by 34.2±4.6 mmol/l, whereas K i + decreases by 37.7±2.2 mmol/l. The results suggest that the application of ouabain is followed by a decrease of peritubular cell membrane permeability to K+, by an accumulation of Ca2+, Na+ and HCO 3 - in the cell and by a dissipation of the electrochemical Cl− gradient.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Frog kidney ; Proximal tubule ; Glucose transport ; Ouabain ; Cell membrane potential ; Intracellular sodium ; Microelectrodes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Inhibition of basolateral Na+/K+ ATPase by ouabain eventually abolishes transport of glucose. The present study was performed to test, if this effect is due to a dissipation of the electrochemical gradient for sodium or due to a regulatory inhibition of sodium-coupled glucose entry across the luminal membrane at increasing intracellular sodium activity. To this end, proximal convoluted tubules of the doubly perfused isolated frog kidney were perfused alternatively with solutions containing either 5 mmol/l glucose or raffinose. The potential difference across the peritubular cell membrane (PDpt) and across the epithelium (PDpt) has been recorded with conventional and across the peritubular cell membrane with ion selective microelectrodes (PDpt). In the absence of luminal glucose PDpt is (±SEM) −54.0±2.4 mV, PDte=−1.2±2.0 mV and PD pt Na =−96±5 mV. The electrochemical gradient for sodium (μNa+) amounts to 95 mV and intracellular sodium activity to 14 mmol/l (extracellular sodium activity is 74 mmol/l). Luminal application of glucose leads to a rapid depolarisation of PDpt (ΔPDpt=8.6±0.9 mV and PD pt Na (ΔPD pt Na =11.1±3.0 mV) and to hyperpolarisation of PDte (ΔPDte=−0.8±0.2 mV). The peritubular application of ouabain leads to a gradual, reversible and proportional decline of PDpt, PD pt Na and μNa+. Glucose induced ΔPDpt and ΔPD pt Na decrease in parallel to PDpt and PD pt Na , resp. In a separate series, the lumped conductance (G m) of the luminal and basolateral cell membrane has been determined, which amounts to 2.4±0.3 μS/mm (tubule length).G m decreases 23±4%, when PDpt is decreased to half. ΔPDpt andG m allow the calculation of an apparent transport rate (T Glu). Following the application of ouabain,T Glu decreases in linear proportion to PDpt and PD pt Na . There is no evidence for a significant regulatory inhibition ofT Glu. Rather, glucose transport operates in linear proportion to the potential difference across the luminal membrane.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 63 (1985), S. 944-947 
    ISSN: 1432-1440
    Keywords: Alcohol ; Ethanol ; Acetaldehyde ; Alcohol dehydrogenase ; Kidney ; Renal tubule ; Alkohol ; Äthanol ; Acetaldehyd ; Alkoholdehydrogenase ; Niere ; Nierentubulus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die renale Behandlung des Äthanols umfaßt sowohl die glomeruläre Filtration als auch die tubuläre Reabsorption. Wegen seiner hohen Permeabilität nähert sich die Konzentration des Alkohols in der Tubulusflüssigkeit derjenigen der peritubulären Flüssigkeit an, und unter Steady-state-Bedingungen ist die Alkoholkonzentration im Endharn fast genau so hoch wie im Serumwasser. Selbst hohe Alkoholkonzentrationen stören die Nierenzellfunktion nicht nennenswert. Das scheint darauf zu beruhen, daß Nierengewebe praktisch keine Alkoholdehydrogenase enthält. Deswegen sammelt sich Acetaldehyd, das zytotoxische Stoffwechselprodukt des Alkohols, nicht in wirksamer Dosis an. Nach direkter Zufuhr im Rahmen von Mikropunktionsexperimenten übt Alkohol keine nennenswerten Wirkungen aus. Demgegenüber blockiert Acetaldehyd die wesentlichen Parameter der Zellvitalität, gemessen in Form der elektrischen Membranpotentiale und der intrazellulären Ionenaktivitäten.
    Notes: Summary The renal handling of ethanol comprises glomerular filtration and tubular reabsorption. Due to its high permeability alcohol concentration in the tubular fluid approaches that of peritubular fluid and under steady state conditions alcohol concentration in the final urine is almost the same as in serum water. Even in high concentrations alcohol does not significantly interfere with kidney cell function. This seems to be due to the fact that renal tissue is almost free from alcohol dehydrogenase. Thus, acetaldehyde, the cytotoxic intermediate of alcohol metabolism, is not accumulated in effective dosis. If applied directly in micropuncture experiments alcohol is without distinct effects while acetaldehyde inhibits the main parameters of cellular vitality as measured by electrical membrane potentials and intracellular ion activities.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 351 (1974), S. 323-330 
    ISSN: 1432-2013
    Keywords: Uricase ; Urate ; Allantoin ; Liver ; Kidney ; Microperfusion ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. In vivo uricase activity was tested in rats by injection of 2-C14 urate and measurement of the total C14 activity and the fractional activities of allantoin, allantoic acid and urea in samples of blood and urine. In control animals, 5 min after the injection, 70% of the plasma tracer was already present in the form of allantoin. No allantoic acid and urea were produced. Intestinectomy had no measurable influence on uricase activity. On the other hand, hepatectomy or ligation of the hepatic artery combined with subtotal viscerectomy did abolish uricase activity almost completely. 2. Following microinjections into proximal tubules of Ringer solution containing 2-C14 urate, urine samples during early recovery mainly contained labelled urate, whereas in later samples the fraction of labelled allantoin increased. About 12 min after the microinjection the urine of both kidneys contained equal amounts of tracer mainly in the form of allantoin. 3. When segments of proximal tubules were perfused with an equilibrium solution containing tracer amounts of C 14 urate, no urate was metabolized during its passage through the proximal tubule. 4. C 14 urate was offered from the peritubular capillaries and samples of tubular fluid were analyzed, Again, all the tracer in the tubular fluid was in the form of urate, indicating that urate is not oxidized when it is transported across the tubular cell. It is concluded from these results that: 1. The rat kidney has no significant uricase activity. 2. Urate transport in the kidney is not influenced by this enzyme. 3. The degradation of urate to allantoin takes place at extrarenal sites, mainly in the liver.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 352 (1974), S. 115-120 
    ISSN: 1432-2013
    Keywords: Urate ; Reabsorption ; Loop of Henle ; Micropuncture ; Microperfusion ; Microinjection ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Reabsorption rates for urate in the loops of Henle were measured in superficial nephrons in the rat 1. under conditions of free flow, 2. using microperfusion and 3. by a microinjection technique. 1. Under conditions of free flow distally measured TF/PUA/TF/PIn-values varied between 0.51 and 0.38 in antidiuretic rats, depending on TF/PIn (UA = both uric acid and urate, In = inulin, TF/P = concentration in tubular fluid to plasma concentration). The corresponding values in samples from end-proximal tubules were 1.06 and in urine 0.19 (U/PUA/U/PIn). 2. In microperfusion experiments of Henle loops early distal recoveries of 2-C14 urate varied between 57 and 86%, depending on the flow rates (10–40 nl/min). 3. In microinjection experiments C14 recovery in urine was about 85% when tracer solution was microinjected into endproximal tubules. From these results we conclude: 1. The main site of urate reabsorption is located in the loops of Henle. 2. This reabsorption is highly dependent on flow rates. Increase of flow rate through Henle's loop decreases urate reabsorption.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 352 (1974), S. 121-133 
    ISSN: 1432-2013
    Keywords: Urate ; Protein Interaction ; Uptake by Erythrocytes ; Renal Reabsorption ; Man ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Interaction of urate with human and rat plasma was studied by a dialysis technique at different temperatures. At 4° C a certain fraction of urate is bound to proteins. However, this fraction diminishes with increasing temperature and at 37° C only some 7–8% (in man) and 2% (in rat) interact with proteins. The finding that urate is almost completely filtered in the glomerulus is discussed. In body areas exposed to low temperatures protein binding of urate may be of importance. Urate uptake by erythrocytes is characterized by two components: a fast component equilibrating almost immediately at about 7% in man and 17% in rat and a slow component reaching equilibrium after 60 min, at 28% and 36%, respectively. The process is described by a mathematical formula. Lowering of the temperature mainly diminishes uptake by the slow component withQ 10-values ranging between 1.5 and 4.0. In the observed range of concentrations the uptake process does not saturate. The results at lower pH-values suggest that it is unionized uric acid which is transported by the slow component. Application of the data to kidney medulla supports the hypothesis that erythrocytes and, probably, to a lesser extent plasma proteins serve as vehicles for urate reabsorption in the countercurrent system. Such a temporary interaction enables uric acid to escape recirculation and to leave the kidney medulla.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 302 (1968), S. 219-232 
    ISSN: 1432-2013
    Keywords: Glucose Reabsorption ; Micropuncture ; Renal Tubule ; Tubular Glucose Concentration ; Glucoseresorption ; Mikropunktion ; Nierentubulus ; Tubuläre Glucosekonzentration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung In Mikropunktionsuntersuchungen an Nieren narkotisierter Ratten wurde die tubuläre Glucosekonzentration bei freiem Harnfluß und bei normaler Plasmakonzentration an verschiedenen Stellen des proximalen Tubulus gemessen. Die Glucosebestimmung erfolgte enzymatisch. Die Glucosekonzentration nahm über die erste Hälfte des proximalen Konvolutes etwa exponentiell bis zu einem Wert von 0,9 mM/l ab und änderte sich in der zweiten Hälfte nicht mehr. Die Glucosekonzentration im Endharn lag ungefähr im gleichen Bereich wie am Ende des proximalen Konvolutes. Ungeachtet des stetigen Abfalles der tubulären Glucosekonzentration zeigte der berechnete Glucosetransport keine Korrelation zur Länge des punktierten Tubulus vom Glomerulum bis zur Punktionsstelle, wenn unterschiedliche Resorptionsraten von Wasser und NaCl provoziert wurden, so daß der Glucosetransport nicht allein von der Masse des resorbierenden Epithels abhängig sein kann. Es wird besprochen, daß neben der Masse des resorbierenden Epithels und der Glucosekonzentration in der tubulären Flüssigkeit die Elektrolytund Wasserresorption bzw. indirekt das Glomerulumfiltrat die Höhe der renalen Glucosereabsorption wesentlich beeinflussen.
    Notes: Summary Glucose concentration was determined enzymatically in tubular fluid samples taken during free-flow micropuncture along the length of the proximal convolution in anaesthetized rats. The glucose concentration decreased exponentially in the first half of the proximal convolution to a mean value of 0.9 mM/l, and did not change in the remaining length accessible to micropuncture. An identical mean value was found in the final urine. When the rates of salt and water reabsorption were varied experimentally, calculated glucose reabsorption showed no relationship to tubular length measured from glomerulum to puncture site. It appears, therefore, that in addition to the mass of reabsorptive tissue and the glucose concentration of tubular fluid, the reabsorption of water and electrolytes plays an important part in determining the rate of glucose reabsorption by the kidney.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 324 (1971), S. 279-287 
    ISSN: 1432-2013
    Keywords: Uric Acid Secretion ; Micropuncture ; Renal Tubule ; Ultramicro Analysis ; Harnsäuresekretion ; Mikropunktion ; Nierentubulus ; Ultramikroanalyse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Mit Hilfe der Mikropunktionstechnik und einer neu entwickelten Methode der Ultramikroanalyse wurde der Harnsäuretransport am proximalen Tubulus der Rattenniere untersucht. Unter normalen Bedingungen ohne Harnsäureinfusion und ohne osmotische Diurese konnte eine Harnsäure-Netto-Sekretion im proximalen Tubulus nachgewiesen werden. Dabei war in diesen Experimenten die Inulinclearance etwa doppelt so groß wie die Harnsäureclearance. In der Bilanz wurde also mehr Harnsäure resorbiert als sezerniert, aber nicht, wie früher angenommen, im proximalen Tubulus.
    Notes: Summary Uric acid transport in the rat proximal tubule was studied by micropuncture and a new method of chemical ultramicro analysis. Under normal free-flow conditions at physiological levels of uric acid plasma concentrations a net secretion of uric acid in the proximal tubule was demonstrated. In these experiments the clearance ratio of uric acid to inulin was in the range of 0.4 which is normal in antidiuretic rats. Net reabsorption of uric acid, therefore, took place in the kidney, but certainly not in the proximal tubule as previously suggested.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 7 (1979), S. 143-148 
    ISSN: 1434-0879
    Keywords: Urate ; Oxalate ; Renal Handling ; Precipitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Both urate and oxalate are organic acids of considerable clinical interest, owing to their limited solubility. Calcium oxalate is the most frequent constituent of renal calculi and occasionally precipitates in body fluids. Urate precipitations are common in the kidney and in various other tissues. In this paper, a short outline of the present knowledge of renal handling of these substances will be followed by some conclusions as to the possible relevance of this knowledge for the understanding of urolithiasis and intrarenal precipitation. Direct (micropuncture) data are available for urate in the rat (1,6, 7, 10, 21, 23, 28, 36, 42), rabbit (35), dog (34) and cebus monkey (33) and in the rat only for oxalate (11, 15, 20).
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