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  • Chemistry  (4)
  • Dopamine  (3)
  • Adrenal Medulla  (1)
  • Catccholamines  (1)
  • 1
    ISSN: 1432-1912
    Keywords: Dopamine ; Secretion ; Adrenal Medulla ; Catecholamine ; Biosynthesis-Rate ; Dopamin ; Sekretion ; Nebennierenmark ; Catecholamine ; Biosyntheserate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Cats and rabbits were injected intravenously with3H-tyrosine and the radioactivity of the catecholamines in adrenal glands and adrenal blood was measured up to 60 min after injection. Adrenal blood was collected in a cava pocket. In addition the specific activity of free3H-tyrosine in blood plasma was measured as a function of time. Radioactive dopamine could be demonstrated in venous blood from adrenals of cat and rabbit by different methods (column chromatography with Dowex 50, paper chromatography, high voltage paper electrophoresis). On the other hand arterial blood flowing to the adrenals contained no3H-dopamine. During the 30 min after the injection of3H-tyrosine cat adrenals secreted about 14% of the synthesized radioactive catecholamines as3H-dopamine and 8% as3H-noradrenaline. In contrast to this the adrenals of rabbits secreted not more than 3% as3H-dopamine and about 20% as3H-noradrenaline. The catecholamine biosynthesis rate of the adrenals and their dopamine resting secretion was estimated from the specific activity of3H-tyrosine in blood plasma and the radioactivity of catecholamines in adrenal glands and adrenal blood. In cats two adrenals synthesized 0.75 mμMol/min catecholamine per kg body weight and in rabbits 0.074 mμMol/min/kg body wt. respectively. The dopamine resting secretion in cats was about 0.08 mμMol/min and in rabbits about 0.002 mμMol/min.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 272 (1972), S. 265-276 
    ISSN: 1432-1912
    Keywords: Erythrocytes ; Catechol-O-Methyl Transferase (COMT) ; Catccholamines ; Isoproterenol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Washed human red cells, suspended in an isotonic electrolyte solution, were incubated with radioactive catecholamines (epinephrine, norepinephrine, dopamine and isoproterenol). Their conversion to 3-O-methyl derivatives was demonstrated by ion exchange chromatography for each substrate. There was no O-methylation if the erythrocytes were boiled or hemolyzed prior to incubation or if the catechol-O-methyl transferase (COMT) inhibitor pyrogallol was added to the incubation medium. Only catecholamines were methylated by this system, as could be demonstrated by using the non-catecholamine orciprenaline as substrate. Experiments with l-methionine-(methyl-14C) showed that the methylation was brought about by the transfer of a methyl group from l-methionine to the 3-hydroxy group of epinephrine. Thus, this enzymatic system had the properties of COMT. Our experiments therefore suggest that COMT is present in human erythrocytes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 277 (1973), S. 373-386 
    ISSN: 1432-1912
    Keywords: Kidney ; Renal Handling ; Dopamine ; Noradrenaline ; Adrenaline ; Catechol-O-Methyl-Transferase (COMT)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In 12 female dogs renal excretion and catabolism of 14C-(±)-adrenaline, 14C-(±)-noradrenaline, 14C-dopamine and 3H-(±)-normetanephrine were investigated using a modified stop-flow technique. Radioactive compounds were infused, together with inulin, into the left renal artery for 10 min. During the first 2 min of the infusion period the left ureter was occluded. Urine samples were serially collected from both kidneys up to the end of the infusion. In the urine the total radioactivity and the pattern of radioactive metabolites were measured. On average, the infused kidney excreted from the infused dose of 14C-adrenaline 9.4% as adrenaline, 27.9% as metanephrine and 5.8% as deaminated or conjugated metabolites. From infused 14C-noradrenaline 7.4% was excreted as noradrenaline, 3.5% as normetanephrine and 1% as deaminated or conjugated compounds. When 3H-normetanephrine was infused the urine contained only radioactive normetanephrine (22.2%). From the infused dose of 14C-dopamine 9.6% was excreted as dopamine, 16.2% as 3-O-methyldopamine and 3.7% as deaminated or conjugated compounds. — Urine from the other kidney contained 1/25 to 1/5 the radioactivity of that from the infused side, but the pattern of radioactive compounds was similar. From the excretion rate of simultaneously infused inulin the filtration fraction of the infused kidney was determined. That part of the infused 14C-catecholamines which was excreted unmetabolized in the urine, corresponds to the filtration fraction in this kidney. Therefore, it is suggested, that in mammals the unmetabolized catecholamines of the urine are mainly excreted by glomerular filtration and not by tubular secretion. On the other hand, the urinary O-methylated radioactive catecholamines, which were excreted by the infused kidney at a high rate, were formed in this organ from the infused catecholamines and were excreted by tubular secretion. Thus, in mammals tubular secretion is linked to an inactivation of these compounds by O-methylation.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 295 (1976), S. 123-126 
    ISSN: 1432-1912
    Keywords: Dopamine ; Kidney ; Metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 14C-Dopamine at a dose between 0.16 and 400 nmol per kg body weight was injected locally into the renal artery and urinary excretion of the label was followed for a period of up to 75 min. During the first renal passage the injected kidney excreted 28.2±8.3% (n=8) of the activity applied. As shown by column chromatography the 14C-activity in urine was mainly present as 3,4-dihydroxyphenyl acetic acid (40%), homovanillic acid (15%) and dopamine (app. 20%). Excretion rate and the pattern of dopamine metabolites in urine was independent of the administered dose. Thus, the excretion of dopamine by the cat kidney is linked to an inactivation by the kidney enzymes MAO and COMT. From the literature it is known that in dog and chicken kidney catecholamines are not metabolized to such a large extent during renal excretion.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 2282-2284 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch katalytische Hydrierung von Acetamino-[4-amino-Δ2-butenyl]-malonsäure-diäthylester-hydrochlorid mit Tritium und anschließende Hydrolyse wurde DL-Lysin-[4.5-T2]-dihydrochlorid dargestellt.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 98 (1965), S. 3200-3203 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch katalytische Hydrierung von α-Acetamino-β-[2-chloracetamino-äthyl]-acrylsäure mit Tritium und anschließende Hydrolyse wurde DL-Ornithin-[α.β-T2] dargestellt. Dieses ließ sich durch Umsetzung mit O-Methyl-isoharnstoff in DL-Arginin-[α.β-T2] überführen.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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