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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 351 (1994), S. 314-316 
    ISSN: 0014-5793
    Keywords: Catalase ; Hydrogen peroxide ; Juxtaglomerular cell ; Oxygen radical ; Renin ; Superoxide dismutase
    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
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 4 (1961), S. 38-42 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 4 (1961), S. 43-47 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 4 (1961), S. 323-327 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0898-6568
    Keywords: EGF ; Glomerular epithelial cell ; TGFβ ; cAMP ; cholera toxin ; forskolin ; heparin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1912
    Keywords: 3H-noradrenaline release ; SHR ; Kidney ; Prejunctional β-adrenoceptors ; Adrenaline ; Isoprenaline ; cAMP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The aim of the present study was to investigate β-adrenoceptor modulation of noradrenaline release from sympathetic nerves in superfused cortical kidney slices of 4-week-old spontaneously hypertensive rats (SHR) and age-matched controls (WKY). After preincubation with 3H-noradrenaline the kidney slices were electrically stimulated in superfusion chambers. The stimulation induced (S-I) outflow of radioactivity was mainly composed of unmetabolized 3H-noradrenaline in both strains and thus taken as an index of noradrenaline release. There was a frequency-dependent (1.25–20 Hz) increase in the S-1 outflow of radioactivity. At all stimulation frequencies tested S-I outflow of radioactivity was similar or even slightly lower in SHR than in WKY kidney slices in either the absence or presence of cocaine (10 μmol/l). The non-selective β-adrenoceptor agonists isoprenaline (0.l gmol/1) and adrenaline (0.01 and 0.1 μmol/l) enhanced S-I outflow of radioactivity. The facilitatory effects of isoprenaline (0.1 μmol/l) and adrenaline (0.1 μmol/l) were blocked by the selective β2-adrenoceptor antagonist ICI 118551 (0.1 μmol/l) but not by the selective β1-adrenoceptor antagonist atenolol (0.3 μmol/l). The cell-permeable CAMP analogue 8-bromo-cAMP (300 μmol/l) enhanced S-1 outflow of radioactivity to a similar extent in both SHR and WKY kidney slices. A combination of 8-bromo-cAMP (300 μmol/l) and adrenaline (0.1 μmol/l) did not enhance S-1 outflow of radioactivity to a greater extent than 8-bromo cAMP (300 μmol/l) alone in both strains. However, the facilitatory effects of isoprenaline (0.1 μmol/l) and adrenaline (0.1 μmol/l) but not that of adrenaline (0.01 μmol/l) were significantly greater in SHR than in WKY. The results suggest that stimulation of prejunctional β2-adrenoceptors by adrenaline even in the absence of a-adrenoceptor blockade enhances noradrenaline release in kidney cortex of young SHR and WKY. This β2-adrenoceptor mediated effect may possibly be dependent on cAMP formation. The greater facilitatory effects of isoprenaline (0.1 μmol/l) and adrenaline (0.1 μmol/l) in SHR as compared to WKY are in accord with receptor binding studies which show a higher density of β2-adrenoceptors in SHR than in WKY kidney cortex.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 58 (1980), S. 1243-1250 
    ISSN: 1432-1440
    Keywords: Purinnukleotidsynthese ; Pentosephosphat-Shunt ; Erythrozyten ; Urämie ; Purine nucleotide synthesis ; Pentose phosphate pathway ; Erythrocytes ; Uremia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Studies were performed which suggest that the increased red cell levels of ATP and adenine nucleotides in uremic patients may be secondary to an increased biosynthetic rate of adenine nucleotides via salvage pathway by the predominance of younger red cells. Both normal and uremic red cells were separated in three groups according to their age by centrifugation in a discontinous density gradient using phthalate esters as separating liquids. 1. The uremic subjects have a substantial reduction of the older (more dense) red cells with a 3–4 fold increase of the younger red cells. 2. The specific activity of the salvage pathway enzymes phosphoribosyl-1-pyrophosphate (PRPP)-synthetase, adenine phosphoribosyltransferase and the red cell PRPP levels are strictly age-dependent and substantially increased in the uremic erythrocytes. No definite alterations of enzyme halflifes of both enzymes could be discerned. No differences were found in the substrate saturation curves between the enzymes of normal and uremic erythrocytes. 3. Red cell methylene-blue stimulated pentose phosphate pathway (PPS) wasn't significantly lower in patients with chronic uremia than in controls, as could be shown by the determination of red cell ribose-5-phosphate concentration. There was no difference of the steady-state levels of ribose-5-phosphate in the age-dependent red cell fractions of both normal and uremic subjects. 4. The results support the assumption that the elevated ATP levels in the uremic red cells may be related to their higher intrinsic ATP synthetic capacity via salvage pathway. 5. The enzymatic alterations in the uremic red cells are independent of extracorpuscular factors including phosphate, and it was concluded that most of the described abnormalities in the uremic red cell metabolism reflect only the hypermetabolic state of a young red cell population. The conflicting results concerning red cell metabolism of uremic patients could be probably caused by an inconstant percentage of younger red cells in various uremic patients.
    Notes: Zusammenfassung Erythrozyten von gesunden Kontrollpersonen und von urämischen Patienten wurden im Dichtegradienten in drei Altersklassen getrennt und die Enzyme des Purinnukleotid-Reutilisierungsstoffwechsels bestimmt: 1. Bei gleichzeitiger Verminderung der Fraktion der alten Zellen war der Anteil der jüngeren Erythrozyten in den urämischen Patienten um das drei- bis vierfache erhöht. 2. In allen Fraktionen der urämischen Erythrozyten waren die spezifischen Aktivitäten der vom Zellalter-abhängigen Enzyme, Phosphoribosyl-1-pyrophosphat (PRPP)-Synthetase, die Adenin-Phosphoribosyltransferase und die intrazellulären Phosphoribosyl-1-pyrophosphat-Konzentrationen deutlich erhöht. Die Halbwertszeiten und die kinetischen Parameter beider Enzyme waren jedoch unverändert. 3. Die Aktivität des Pentosephosphat-Shunts (PPS), gemessen an den intrazellulären Ribose-5-phosphat-Konzentrationen, war in den Erythrozyten urämischer Patienten nicht signifikant verändert. Nach Aktivierung des Pentosephosphat-Shunts durch Methylenblau (10−4 M) werden in allen Erythrozyten-Fraktionen gleiche Steigerungsraten festgestellt, wobei die intrazellulären Phosphoribosyl-1-pyrophosphat-Konzentrationen bei physiologischen Serumphosphatspiegeln unverändert bleiben. 4. Die Versuche zeigen, daß als Ursache erhöhter intraerythrozytärer ATP — Spiegel in Urämie-Patienten eine gesteigerte Adeninnukleotidsynthese durch einen verstärkten “salvage-pathway” angenommen werden kann. 5. Unsere Ergebnisse weisen darauf hin, daß die hypermetabolische Aktivität der Erythrozyten niereninsuffizienter Patienten Ausdruck einer jüngeren Erythrozyten-Population ist.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 59 (1981), S. 1223-1224 
    ISSN: 1432-1440
    Keywords: Hydrochlorothiazide ; Pharmacokinetic ; Phenytoin ; Hydrochlorothiazid ; Pharmakokinetik ; Phenytoin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bei 7 gesunden Freiwilligen wurden Plasmaspiegel und Urinausscheidung von Hydrochlorothiazid gemessen. In randomisierter Reihenfolge wurden 75 mg Hydrochlorothiazid mit und ohne vorausgegangener 6tägiger Phenytoin-Therapie (300 mg/die) oral verabreicht. Es fanden sich große intra- und interindividuelle Unterschiede in der Bioverfügbarkeit von HCT (32–87% bzw. 42–77%), Phenytoin zeigte jedoch keinen Einfluß auf die Dispositionsparameter des Diuretikums.
    Notes: Summary Plasma levels and urinary recovery of Hct were determined in seven healthy male volunteers. 75 mg Hct were administered as a tablet in a randomised fashion with or without phenytoin pretreatment (300 mg/d). Bioavailability of Hct showed considerable intra- and interindividual variation (32–87% and 42–77% respectively), but phenytoin did not influence the disposition parameters of the diuretic.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-198X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-1912
    Keywords: Rat kidney ; α-Adrenoceptors ; Noradrenaline release ; Prostaglandins ; Purines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of the at-adrenoceptor agonist methoxamine and the α2-adrenoceptor agonist bromoxidine (UK 14034) on the stimulation induced (S-1) outflow of radioactivity at 100 Hz/6 pulses from rat isolated kidney preincubated with 3H-noradrenaline were investigated. Methoxamine (0.3 – 30 μmol/l) inhibited S-1 outflow of radioactivity to a maximum of 83% with a pEC50 of 5.85 (5.71–5.94). UK 14304 (0.0003-0.3 μmol/l) inhibited S-I outflow of radioactivity to a maximum of 99% with a pEC50 of 8.35 (8.26–8.47). a Adrenoceptor antagonist affinities (pKD) against methoxamine and UK 14304 at prejunctional α-adrenoceptors were determined. The concentration response curve of methoxamine was shifted to the right by the α1/α2B-adrenoceptor antagonist prazosin (0.1 μmol/l) with a pKD of 7.41 and that of UK 14304 by prazosin (0.3 μmol/l) with a pKD of 6.24. The α2-adrenoceptor antagonist rauwolscine (0.1 μmol/l) shifted the concentration response curve of UK 14304 potently to the right with a pKD of 8.34. The concentration response curve of methoxamine was shifted also to the right by rauwolscine (0.1 μmol/l) and the α2-adrenoceptor antagonist idazoxan (0.1 μmol/l), however, both antagonists suppressed the maximum response of methoxamine to 466% and 56%, respectively. A ten times lower concentration of rauwolscine (0.01 μmol/l) did not shift the concentration response curve of methoxamine but the inhibitory effect of methoxamine still reached only a maximum of 59%. The concentration response curve of methoxamine obtained in the presence of rauwolscine (0.01 μmol/l) was shifted to the right by further addition of prazosin (0.1 μmol/l) with a pKD of 8.80 but was also shifted to the right by either the purinoceptor antagonist 8-(p-sulfophenyl) theophylline (8-SPT; 100 μmol/l) or the prostaglandin synthesis inhibitor indomethacin (20 μmol/l). These results suggest that methoxamine inhibits S-1 outflow of radioactivity in rat isolated kidney probably through three different mechanisms. 1. Activation of postjunctional α1-adrenoceptors and prostaglandin mediated transjunctional inhibition. 2. Activation of postjunctional α2-adrenoceptors and purine mediated transjunctional inhibition. 3. Activation of prejunctional inhibitory α2-adrenoceptors at which methoxamine seems to be a partial agonist.
    Type of Medium: Electronic Resource
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