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  • 1
    ISSN: 1432-2072
    Keywords: Acetorphan ; Enkephalinase inhibition ; Opioid withdrawal ; Naloxone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of 60 min pretreatment with the enkephalinase inhibitor acetorphan were assessed on naloxone-precipitated (2.5 mg/kg IP) abstinence in chronically morphinized rats. In addition, the antinociceptive activity of the compound was investigated in mice. Intraperitoneal injection (50 mg/kg) in rats attenuated some aspects of the opioid withdrawal syndrome such as burrowing, wet dog shakes, squeal on touch hostility, tachypnoea, ptosis and rough hair, whereas jumping and escape behaviour were significantly increased in acetorphan-treated animals. No effect was observed on withdrawal hypothermia or acute weight loss. Similarly, chronic dosing with acetorphan after withdrawal produced no significant effect on body weight. Acetorphan (50 mg/kg IP) failed to produce any antinociceptive activity in the mouse tail immersion test, but potentiated the antinociceptive effect of d-Ala2-d-Leu5-enkephalin. These results are discussed in terms of acetorphan crossing the blood-brain barrier before being hydrolysed to thiorphan, thus yielding opioid withdrawal relieving effects.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 71 (1985), S. 26-30 
    ISSN: 1432-2242
    Keywords: Chloroplast ; Ribosomal proteins ; Tobacco ; Interspecific differences
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The large subunits (50S) of chloroplast ribosomes were isolated from Nicotiana tabacum, a species of the Western Hemisphere, and from N. excelsior and N. gossei, Australian species. Their proteins were compared by two-dimensional gel electrophoresis. A pair of proteins (T12 and T12) observed in N. tabacum has electrophoretic mobilities which differ from those of a similarly migrating, and probably homologous, pair of proteins observed in N. excelsior and N. gossei. The species-specific proteins in N. tabacum differ slightly in electrophoretic mobilities based on both charge and molecular weight from those in N. excelsior and N. gossei. Tryptic digests of radioiodinated proteins reveal that the peptide maps of all six proteins are similar. These results suggest that chemically altered forms of one or more proteins of the 50S chloroplast ribosome subunit may exist in vivo.
    Type of Medium: Electronic Resource
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