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  • Electronic Resource  (2)
  • 1970-1974  (2)
  • 5-Hydroxytryptophan  (1)
  • Acridizinium-Ions  (1)
  • 1
    ISSN: 1432-1912
    Keywords: DOPA ; 5-Hydroxytryptophan ; Tyrosine Hydroxylase in Rat Brain ; Tryptophan Hydrolyxase in Rat Brain ; NSD 1015 (3-hydroxybenzylhydrazine)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary DOPA and 5-HTP accumulated in vivo in rat brain after decarboxylase inhibition with NSD 1015 (3-hydroxybenzylhydrazine). This accumulation was linear for the first 30 min and occurred in several brain regions over a wide range of NSD 1015 doses. After a peripheral decarboxylase inhibitor much less, if any, DOPA or 5-HTP accumulated in the brain. The accumulation of DOPA was prevented by H 44/68 (methylester of α-methyl para-tyrosine), a tyrosine hydroxylase inhibitor. DOPA, which accumulated before H 44/68 was given, appeared stable for at least 20 min. There were no significant changes in the levels of NA, DA, 5-HT or tryptophan shortly after NSD 1015 administration, but a rise in tyrosine was noted. Increased brain tyrosine after l-tyrosine administration did not alter the DOPA accumulation, however. These data as well as the distribution of the accumulated amino acids suggest that the accumulation of DOPA and 5-HTP after decarboxylase inhibition occurs intraneuronally, that the decarboxylase enzyme is completely inhibited, and that the accumulated products are not appreciably metabolized or transported from the region studied. Amine synthesis rates and rate constants were calculated from the data and compare well with similar values determined by other methods. Thus this accumulation appears to be a reliable measure of the in vivo hydroxylation of tyrosine and tryptophan.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 264 (1973), S. 29-32 
    ISSN: 1618-2650
    Keywords: Verhalten des Benzo[b]chinolizinium-Ions ; Acridizinium-Ions ; Polarographie ; Cycl. Voltammetrie ; Elektronen-Spinresonanz
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary In aprotic solvents, polarography and cyclic voltammetry indicate a two step reduction of acridizinium ion. The first reduction is a reversible one-electron step. The second involves two electrons and is irreversible. In situ ESR electrolysis at the potential of the first reduction gives no evidence of free radicals. Homogeneous chemical reduction of acridizinium by titration with sodium biphenylide indicates a one-electron reduction mechanism in solution. The absence of stable free radicals suggests a rapid post-reduction of the product. Addition of small amounts of water changes the aprotic solvent (mercury electrode) mechanism. The first wave becomes a two-electron irreversible wave at the expense of the second wave. In aqueous solvents two two-electron, irreversible reduction waves occur. Products of the second absorb and change the mechanism after the first CV scan.
    Notes: Zusammenfassung In aprotischen Lösungsmitteln wird durch Polarographie und cyclische Voltammetrie eine zweistufige Reduktion des Acridizinium-Ions angezeigt. Die erste Stufe ist reversibel und bezieht sich auf ein Elektron, die zweite Stufe umfaßt 2 Elektronen und ist irreversibel. Durch in situ ESR-Elektrolyse beim Potential der ersten Stufe konnte kein Beweis für freie Radikale gefunden werden. Homogene chemische Reduktion durch Titration mit Natriumbiphenylid deutet auf einen einelektronigen Reduktionsmechanismus hin. Durch Zugabe kleiner Wassermengen wird die erste Stufe auf Kosten der zweiten irreversibel und zweielektronig. In wäßrigen Lösungsmitteln treten 2 zweielektronige irreversible Reduktionsstufen auf.
    Type of Medium: Electronic Resource
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