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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Bioelectrochemistry and Bioenergetics 17 (1987), S. 419-427 
    ISSN: 0302-4598
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 382 (1979), S. 115-121 
    ISSN: 1432-2013
    Keywords: l-proline reabsorption ; Renal tubule ; Microperfusion ; Transport kinetics ; Diisopropylphosphorofluoridate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Renal tubular reabsorption of3H and14C labelledl-proline was measured in vivo et situ by continuous microperfusion of single proximal tubules of the rat. The reabsorption is shown to be saturable. Passive diffusion plays a relatively small role in the reabsorption. A maximum possible permeability coefficient of 25 μm2·s−1 for proline was calculated. Two transport systems were found, one with a small affinity and a high capacity, the other with a very high affinity and a small capacity. The following values were estimated: $$\begin{gathered} J_{\max 1} = {\text{ }}2.6 \pm 0.28{\text{ }}(SEM){\text{ }}nmol \cdot m^{ - 1} \cdot s^{ - 1} \hfill \\ K_{m1} {\text{ }} = {\text{ }}11.8 \pm 1.7{\text{ }}(SEM){\text{ }}nmol \cdot 1^{ - 1} \hfill \\ J_{\max 2} = {\text{ }}9.6 \pm 1.92{\text{ }}(SEM){\text{ }}pmol \cdot m^{ - 1} \cdot s^{ - 1} \hfill \\ K_{m2} {\text{ }} = {\text{ }}29.3 \pm 7.8{\text{ }}(SEM){\text{ }}\mu mol \cdot l^{ - 1} \hfill \\ \end{gathered} $$ Whereas the first system reabsorbs the bulk of the filtered load, the activity of the second system explains the extremely small amount of proline found in the final urine. Diisopropylphosphorofluoridate — a specific inhibitor of dipeptidyl peptidase IV — decreases the reabsorption ofl-proline andl-alanine but has no influence on the reabsorption of the basic amino acidl-arginine and the acidic amino acidl-glutamic acid. This result correlates with a recent speculation that dipeptidyl peptidase IV is involved in proline and alanine reabsorption.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2013
    Keywords: Amino acid transport ; Renal tubule ; Stereospecificity ; Passive diffusion ; Saturation kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Renal tubular reabsorption of glycine and of thel- andd-isomers of histidine, serine, phenylalamine, methionine, proline and cystine was investigated in vivo et situ by continuous microperfusion of single proximal convolutions of the rat kidney. In the case of glycine and thel-isomers, tubular reabsorption is saturable to a great extent. Thed-amino acids are reabsorbed much more slowly than the respectivel-forms. Furthermore in the case of methionine and perhaps also of proline, serine and phenylalanine, the fractional reabsorption decreases in the presence of high concentrations of thel-form. This indicates that thed-isomers also have a measurable affinity for the reabsorption mechanisms of the renal tubule. The very poor reabsorption ofd-amino acids in the presence of theirl-isomers indicates that simple passive diffusion plays only a relatively small role in tubular amino acid reabsorption. Permeability coefficients estimated from these findings are in the range from 1–5×10−7 cm2·s−1. These values are very similar to those found for other organic molecules of comparable molecular weights.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2013
    Keywords: Proximal tubule ; Kidney ; K+ conductance ; Cell membrane potential ; Ouabain temperature ; Phlorizin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In isolated perfused segments of the mouse proximal tubule, the potential difference across the basolateral cell membrane (PDbl) was determined with conventional microelectrodes. Under control conditions with symmetrical solutions it amounted to −62±1 mV (n=118). The potential difference across the epithelium (PDte) was −1.7±0.1 mV (n=45). Transepithelial resistance amounted to 1.82±0.09 kΩ cm (n=28), corresponding to 11.4±0.6 Ω cm2. Increasing bath potassium concentration from 5 to 20 mmol/l depolarized PDbl by +24±1 mV (n=103), and PDte by +1.6±0.1 mV (n=19). Thus, the basolateral cell membrane is preferably conductive to potassium. Rapid cooling of the bath perfusate from 38°C to 10°C led to a transient hyperpolarization of PDbl from −60±1 to −65±1 mV (n=21) within 40 s followed by gradual depolarization by +18±1% (n=14) within 5 min. The transepithelial resistance increased significantly from 1.78±0.11 kΩ cm to 2.20±0.21 kΩ cm (n=15). Rapid rewarming of the bath to 38°C caused a depolarization from −61±2 mV (n=17) to −43±2 mV (n=16) within 15 s followed by a repolarization to −59±2 mV (n=10) within 40 s. Ouabain invariably depolarized PDbl. During both, sustained cooling or application of ouabain, the sensitivity of PDbl to bath potassium concentration decreased in parallel to PDbl pointing to a gradual decrease of potassium conductance. Phlorizin hyperpolarized the cell membrane from −59±2 to −66±1 mV (n=13), virtually abolished the transient hyperpolarization under cooling, and significantly reduced the depolarization after rewarming from +17±2 mV (n=16) to +9±3 mV (n=9). The present data indicate that the contribution of peritubular potassium conductance to the cell membrane conductance decreases following inhibition of basolateral (Na++K+)-ATPase. Apparently, cooling from 37° to 10°C does not only reduce (Na−+K+)-ATPase activity but in addition luminal sodium uptake mechanisms such as the sodium glucose cotransporter. As a result, cooling leads to an initial hyperpolarization of the cell followed by depolarization only after some delay.
    Type of Medium: Electronic Resource
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