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  • 2000-2004  (1)
  • 1970-1974  (2)
  • 1960-1964
  • Polymer and Materials Science  (2)
  • sympathetic nerve.  (1)
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  • 2000-2004  (1)
  • 1970-1974  (2)
  • 1960-1964
  • 1980-1984  (1)
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  • 1
    ISSN: 1432-0428
    Keywords: Keywords Atropine ; C peptide ; CRF ; footshock ; parasympathetic nerve ; sympathetic nerve.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Aims/hypothesis. To investigate whether proinsulin C peptide influences sympathetic nerve activity directly or indirectly through parasympathetic nerve activity. Methods. The proliferative response of splenic lymphocytes to Concanavalin A (ConA response) which is known to be suppressed by subjection of rats to footshock or intracerebroventricular injection of corticotropin-releasing factor through sympathetic nerve activation was measured. Effect of C peptide alone or before subjection to footshock or injection of corticotropin-releasing factor was examined. Results. Intraperitoneal injection of C peptide was without effect on the basal ConA response, while subjection to footshock or injection of corticotropin-releasing factor lowered it. In contrast, prior injection of C peptide obviated the footshock and corticotropin-releasing factor-induced suppression of the response. When given intracerebroventricularly, C peptide was also effective at much smaller doses. Prior injection of atropine cancelled the C-peptide effects. Conclusion/interpretation. Our results indicate that C peptide counteracts the sympathetic nerve-mediated suppression of splenic lymphocyte proliferation in an atropine-sensitive manner. Thus, C peptide probably activates the parasympathetic nervous system through the afferent mechanism, that in turn antagonizes the sympathetic nerve-mediated suppression of splenic lymphocyte functions. [Diabetologia (2000) 43: 1512–1517]
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 2065-2072 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: For the rapid identification of additives such as antioxidant, ultraviolet absorber, and slipping agent, polypropylene containing such additives was heated in a tube connected directly to the inlet system of a mass spectrometer. The vapor of the additives evaporating out of the polypropylene was led to the reservoir and then submitted to mass spectrometry to give spectra for identification.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 2513-2520 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Gel permeation chromatography, using polystyrene gel and tetrahydrofuran as solvent, has been applied to hydroxybenzophenones, esters of salicylic acid, alkylphenols, alkylated methylenediphenols, and phenol-formaldehyde condensation products. The difference between the calculated molecular volume of these phenolic compounds and that obtained by actual determination with GPC has been ascribed to tetrahydrofuran solvation of the phenolic hydroxyl group. Furthermore, it has become clear that THF solvation is affected by the steric hindrance of ortho-substituted phenol and by inactivation of the phenolic hydroxyl group resulting from internal hydrogen bonding.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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