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  • 11
    ISSN: 1432-0738
    Keywords: Deltamethrin ; In vivo oxidative drug metabolizing activity ; Urinary antipyrine metabolites ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effect of deltamethrin pretreatment on the pharmacokinetics and metabolism of antipyrine was studied in male rats. The total plasma clearance of antipyrine was significantly decreased by deltamethrin pretreatment (20 mg/kg and 40 mg/kg daily for 6 days prior to antipyrine administration), while the elimination half-life at β phase, the area under the concentration-time curve and the mean residence time of antipyrine were significantly increased. The magnitude of the observed changes was dose dependent. The urinary excretion of norantipyrine, 4-hydroxyantipyrine and 3-hydroxymethylantipyrine was decreased by 39%, 32% and 26%, respectively (p〈0.001) in the presence of deltamethrin. In addition, the rate constants for formation of each of these metabolites were significantly decreased by an average of approximately 71%. These results suggest that deltamethrin is capable of inhibiting oxidative metabolism, a finding which could be of clinical and toxicological significance.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: During embryonic tooth formation, interactions between epithelial and mesenchymal cells results in the formation of a metachromatic interface or extracellular matrix. The cervical or germinative region of this epidermal organ system is populated by an increasing gradient of cellular differentiation and an extracellular matrix which is the progenitor for subsequent dentine organic matrix formation. Embryonic rabbit tooth primordia can be maintained in culture enabling kinetic studies of labeled precursor incorporation. Autoradiographs of tooth organ cultures continusly incubated with labeled uridine for periods up to eight hours, demonstrated initial cellular incorporation with subsequent transfer of 2% of the grain density to the extracellular matrix by four hours. The grain density was removed by ribonuclease treatment. No incorporation of tritiated thymidine into the matrix was observed. The incorporation of C14-uridine during organ culture was inhibited by actinomycin D. Micrurgy was employed to isolate the extracellular matrix free of adherent cells. Electron microscopy demonstrated membrane-bound, electron dense bodies within the matrix, presumably cytoplasmic extensions. No cells per se were observed on the isolated matrix. Several experimental criteria suggested that uridine incorporation into the extracellular matrix was regulated by epithelial and mesenchymal cells. Phenol extraction procedures of labeled cervical matrices demonstrated an ultraviolet absorption maximum at 260 μU. Both spectrophotometric determinations and orcinol assays found RNA to be 0.4-0.5% of the cervical extracellular matrix.These results are interpreted to indicate that RNA is a component of the metachromatic extracellular matrix during epithelio-mensenchymal interactions associated with tooth formation. The functional significance of these observations is premature at this time.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The fine structure of the extracellular matrix during epithelio-mesenchymal interactions in the rabbit embryonic tooth germ is described using light and electron microscopy. Observations are restricted to the labial cervical loop region at the bell stage of development in maxillary and mandibular incisor tooth germs. Histochemical methods demonstrate a PAS-positive basement membrane between outer enamel epithelial cells and adjacent undifferentiated mesenchymal cells. The metachromatic region circumscribes the dental papilla region, becoming more intense and wider in association with cells illustrative of more advanced stages of differentiation. Ultrastructural observations of the basal lamina associated with outer enamel epithelial cells, cervical proliferating epithelial and mesenchymal cells, and with inner enamel epithelial cells and pre-odontoblasts are reported. The characteristic mesenchymal filopodia appeared in close proximity to the basal lamina. Microfibrils are seen as depositions on the basal lamina and in association with filopodia. The concentration of intercellular microfibrils is increased when in association with epithelia showing advanced differentiation. Collagen fibrils are frequently noted in peripheral association with mesenchymal cells but not adherent to the basal lamina. Numerous homotypic and heterotypic cell junctions are seen. An understanding of intercellular communication between heterotypic cells may be enhanced by postulating a dual developmental origin for the microfibrils associated with the basal lamina. The under surface of the basal lamina facing the extended mesenchymal filopodia appears to be a significant factor during epithelio-mesenchymal interactions, subsequent extracellular matrix formation, and morphogenesis.
    Type of Medium: Electronic Resource
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