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  • 1
    ISSN: 1432-2013
    Keywords: Renal Tubule ; Phosphate Transport ; Sodium Dependence ; Micropuncture ; Microperfusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The standing droplet method has been used in combination with the peritubular perfusion of blood capillaries to determine the build up of transtubular concentration differences of phosphate (P i ) in the renal proximal convoluted tubule of parathyroidectomized rats. Electron probe analysis was used to estimate P i . At zero time both the intraluminal and the contraluminal P i concentration was 2 mM. The time dependent decrease of the intraluminal P i concentration was approximately 4 times faster in the early than in the late proximal convoluted tubule. After 45 sec an intraluminal steady state concentration of 0.20 mM P i was achieved in the early part. In the late part the intraluminal P i concentration approached a steady state value of 0.54 mM at 120 sec. When sodium free solutions were used the intraluminal P i concentration increased to 2.22 mM in the earlier and to 2.76 mM in the late part. The data indicate that in the proximal convoluted tubule 1. The rate of phosphate reabsorption is greater in the early part than in the later part, and 2. phosphate reabsorption might occur as co-transport with Na+ ions.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Renal tubule ; Phosphate transport ; pH dependence ; Micropuncture ; Microperfusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Early loops of the proximal convoluted tubule of parathyroidectomized rats (PTX-rats) were microperfused with a phosphate (4 mM) containing perfusate. With a perfusion solution of pH around 7.45 as estimated as anion deficit theP i reabsorption was two times greater than with a perfusion solution of pH around 6.85. TheP i reabsorption is reduced in PTX-rats made chronic alkalotic (PTX-cA-rats) but the same pH dependence ofP i reabsorption was found. The data indicate that the divalent phosphate is preferentially reabsorbed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 401 (1984), S. 333-339 
    ISSN: 1432-2013
    Keywords: Low molecular weight protein ; Lysozyme ; Renal reabsorption, accumulation and degradation ; Tyrosine ; Gentamicin ; Inhibition of lysozyme degradation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Previous renal clearance studies provided quantitative data concerning renal reabsorption of proteins while the simultaneous processes of renal accumulation and degradation remain, to a great extent, insufficiently investigated. Thus, it was the aim of this study to measure renal reabsorption of egg-white lysozyme at various lysozyme concentrations and to relate the corresponding accumulation and degradation of lysozyme to the lysozyme transport rates in intact rats and isolated perfused rat kidneys. Lysozyme (with125I-lysozyme in certain experiments), was continuously infused i.v. or added to the perfusate to achieve plasma (or perfusate) concentrations of lysozyme (PLY) of approximately 50, 500 or 1000 mg·l−1 for periods of time varying between 3 and 120 or 150 min. Clearances of inulin and lysozyme or the total content of radioactivity and the trichloroacetic acid (TCA)-soluble radioactivity in the kidney tissue were determined at the end of clearance or accumulation periods. Additionally the perfusate concentration of the metabolite tyrosine was measured by high performance liquid chromatography (HPLC). The reabsorption rates of lysozyme (TLY) were concentration-dependent in both intact rats and isolated perfused rat kidney. After 25 min of lysozyme infusion, the lysozyme reabsorption rates amounted to 37, 245 and 331 μg·min−1·g−1 kidney at the above lysozyme concentrations. After the same infusion time, the accumulation rates of lysozyme were 8, 59 and 118 μg·min−1·g−1 kidney. The difference between the transport rate and accumulation rate should represent the renal degradation rate of lysozyme. The renal accumulation and degradation of lysozyme appeared to increase in a time- and concentration-dependent manner. The renal lysozyme degradation is of limited capacity as shown by measuring directly the release of the amino acid tyrosine by using HPLC. Renal degradation of lysozyme was almost totally inhibited by gentamicin in the presence of significant transport of lysozyme. The results of this study also demonstrate the ability of the rat kidney to reabsorb and accumulate large amounts of the cationic low molecular weight protein lysozyme without ultrastructural changes at plasma concentrations of lysozyme as high as 500 mg·l−1. Transmission electron microscopy indicated an increase in the number of endocytic vesicles and lysosomes at 1000 mg·l−1 plasma concentration of lysozyme after a 30 min infusion.
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    ISSN: 0005-2736
    Keywords: (Rat kidney cortex) ; Amino acid effect ; Endocytosis ; Enzyme-membrane interaction ; Lysozyme ; Protein reabsorption
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0005-2736
    Keywords: (Rat kidney cortex) ; Brush-border membrane ; Endocytosis ; Lysozyme ; Membrane-protein interaction ; Protein absorption
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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