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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Lung 148 (1973), S. 223-226 
    ISSN: 1432-1750
    Keywords: Chemical Mutagens ; Dominant Lethal Mutations ; Host-Mediated Assay ; Mutations ; Point Mutations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Isoniazid erhöhte in der intra-animalen Kultur (host-mediated assay) mit Salmonella typhimurium G 46 als Indicatororganismus die Mutationsfrequenz, löste dagegen nach Applikation an männliche Mäuse keine dominanten Letalmutationen aus. In stärkerem Maß erzeugte Hydrazin Mutationen in der intra-animalen Kultur. Im host-mediated assay werden die Mutationen nur an Mikroorganismen induziert und nachgewiesen; der Befund kann aber nur Hinweis auf eine mögliche mutagene Wirkung am Menschen sein. Da die Substanz jedoch weiten Bevölkerungskreisen verabreicht wird, ist eine gründliche Untersuchung der mutagenen Eigenschaften des INH erforderlich.
    Notes: Abstract Isoniazid showed mutagenic activity in submammalian test systems. If these results were also applicable to man, the mutational load of the population due to isoniazid would be rather large, because this is a widely used agent. We, therefore, carried out mutation experiments in mice, using two different test systems: the dominant lethal test and the host-mediated assay with Salmonella typhimurium G 46 as indicator organism. These methods were chosen because we intended to cover two different spectra of mutations: point mutations and dominant lethal mutations which are thought to be the result of chromosome aberrations. Isoniazid was mutagenic in the host-mediated assay after a total dose of 25–150 mg/kg s. c., but did not induce dominant lethal mutations in mice.In vitro, isoniazid did not show mutagenic activity in this microbial strain, whereas hydrazine was strongly mutagenic in vitro as well as in vivo. The mutagenicity of isoniazid in the host-mediated assay may be explained by the formation of hydrazine in the mouse organism. Although in the host-mediated assay the mammalian metabolism is taken into account, the mutations are induced in microorganisms. Thus we have only indications but no real proof that isoniazid is mutagenic in mammals. These findings do, however, call for profound and critical studies to elucidate the question of whether isoniazid could be mutagenic for man.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 16 (1972), S. 43-48 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 48 (1970), S. 1209-1216 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary The application of 1.13 mM/kg folic acid or xanthopterine causes an acute renal failure in rats which is reversible and connected with changes of the tissue electrolytes. Immediately after application of pteridines an oligo-anuric phase lasting for 15 hours sets in and is followed by a hyposthenuric-diuretic phase. The oligoanuric phase is characterized by a decrease of glomerular filtration rate and by retention of fluid and electrolytes. In the diuretic phase, 4 days after injection of folic acid the sodium and fluid balances are equalized. The inability to concentrate the urine and the increase of rest nitrogen in the serum are normalized 14 days after application of folic acid. 21 days after folic acid a decrease of the GFR can not longer be observed. In the early diuretic phase the changes in the tissue electrolytes consist of a decrease of the extracellular, an increase of the intracellular sodium concentration and a decrease of the extra- and intracellular potassium concentration. The absolute amount of tissue sodium is unchanged while the absolute tissue potassium is decreased. The changes in the electrolytes are partially due to tissue catabolism. The affected reabsorption and secretion after folic acid could be localized in the ascending part of the Henle's loop and in the proximal tubule by experiments with the diuretics furosemide, chlorothiazide and amiloride.
    Notes: Zusammenfassung Die Applikation von 1,13 mM/kg Folsäure bzw. Xanthopterin erzeugt bei Ratten ein akutes Nierenversagen, das reversibel ist und mit Elektrolytveränderungen im Gesamtorganismus einhergeht. Unmittelbar nach der Pteridinverabreichung kommt es zu einer oligoanurischen Phase von 15 Std, der eine hyposthenurisch-diuretische Phase folgt. Die oligoanurische Phase ist gekennzeichnet durch eine Einschränkung der glomerulären Filtration sowie durch Flüssigkeits- und Elektrolytretentionen. In der diuretischen Phase sind die Natrium- und Flüssigkeitsbilanzen nach 4 Tagen ausgeglichen. Eine bestehende Konzentrierungsschwäche und die anfänglich vorhandene Rest-Stickstofferhöhung im Serum sind 14 Tage nach der Folsäuregabe wieder normalisiert. Nach 21 Tagen ist die Senkung der glomerulären Filtration nicht mehr nachweisbar. Die Veränderungen der Gewebselektrolyte in der frühen diuretischen Phase bestehen in einer Verminderung der extracellulären und Erhöhung der intracellulären Natriumkonzentration bei unverändertem Gesamt-Natrium sowie in einer Verminderung der intraund extracellulären Kaliumkonzentration bei erniedrigtem Gesamt-Kalium und sind zum Teil durch Gewebsabbau in den ersten 96 Std nach Folsäuregabe bedingt. Durch Versuche mit den Diuretica Furosemid, Chlorothiazid, Amilorid wurden die durch Folsäure beeinträchtigten reabsorptiven und sekretorischen Tubulusfunktionen in den aufsteigenden Teil der Henleschen Schleife und in den proximalen Tubulus lokalisiert.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 117 (1972), S. 197-209 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A selection of mono- and polyfunctional alkylating agents as well as a folic acid antagonist and an acridine derivate were tested with the host-mediated assay, and as far as not known from the literature, with the dominant lethal test for mutagenic activity in mice. In the host-mediated assay system the indicator organisms Salmonella typhimurium G46 His −, Serratia marcescens a 13 His − and a 21 Leu − were used as back mutation systems and E. coli 343 as a forward mutation system. We found indications that polyfunctional alkylating agents induce dominant lethal mutations to a larger extent, whereas monofunctional alkylating agents revealed more mutagenic activity on the molecular level. No definite mutagenicity could be observed for amethopterine, which is mutagenic in cytogenetic investigations. Trypaflavin which is known to be mutagenic in the dominant lethal test, did not induce point mutations in our indicator strains. We conclude that the spectra of mutations, which can be recognized by these two methods, overlap only partially.
    Type of Medium: Electronic Resource
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