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  • Polymer and Materials Science  (2)
  • insulin responses  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of mammary gland biology and neoplasia 2 (1997), S. 265-278 
    ISSN: 1573-7039
    Keywords: Pregnancy ; lactation ; glucose metabolism ; insulin responses ; homeorhesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Increased glucose requirements of the gravid uterus during late pregnancy and even greater requirements of the lactating mammary glands necessitate major adjustments in glucose production and utilization in maternal liver, adipose tissue, skeletal muscle, and other tissues. In ruminants, which at all times rely principally on hepatic gluconeogenesis for their glucose supply, hepatic glucose synthesis during late pregnancy and early lactation is increased to accommodate uterine or mammary demands even when the supply of dietary substrate is inadequate. At the same time, glucose utilization by adipose tissue and muscle is reduced. In pregnant animals, these responses are exaggerated by moderate undernutrition and are mediated by reduced tissue sensitivity and responsiveness to insulin, associated with decreased tissue expression of the insulin-responsive facilitative glucose transporter, GLUT4. Peripheral tissue responses to insulin remain severely attenuated during early lactation but recover as the animal progresses through mid lactation. Specific homeorhetic effectors of decreased insulin-mediated glucose metabolism during late pregnancy have yet to be conclusively identified. In contrast, somatotropin is almost certainly a predominant homeorhetic influence during lactation because its exogenous administration causes specific changes in glucose metabolism (and many other functions) of various nonmammary tissues which faithfully mimic normal adaptations to early lactation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 19-30 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyamides of both cis- and trans-1,4-cyclohexanebis(methylamine) with aliphatic dicarboxylic acids and copolyamides of trans-1,4-cyclohexanebis(methylamine) with p-xylene-α,α′-diamine were prepared in order to discover the effect of cycloalkane rings on melting point. Analogous polyamides of p-xylene-α,α′-diamine were prepared for comparison. The polyamides of trans-1,4-cyclohexanebis(methylamine) had higher melting points than the analogous polyamides of p-xylene-α,α′-diamine. This result is believed to be due to the slightly contracted conformation which trans-1,4-cyclohexanebis(methylamine) can adopt in the polymer chain. The polyamides of cis-1,4-cyclohexanebis(methylamine) melted lower than those of the trans isomer. The lower symmetry of the cis-diamine accounts for this result. The melting points of the copolyamides of trans-1,4-cyclohexanebis(methylamine) and p-xylene-α,α′-diamine were higher than expected. It is suggested that these compositions are examples of partially isomorphous copolyamides.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 2115-2125 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of polyesters of trans-1,4-cyclohexanedimethanol was prepared and the melting points compared with those of the analogous series of polyesters prepared from p-xylylene glycol. Only slight differences in melting points were noted between the corresponding pairs of polyesters prepared from a single aliphatic dicarboxylic acid and from the two glycols. However, polyesters derived from aromatic dibasic acids and trans-1,4-cyclohexanedimethanol melt at a higher temperature than the corresponding polymer from p-xylylene glycol. The probable molecular configuration of polyesters based on trans-1,4-cyclohexanedimethanol is discussed. It is suggested that the diol moiety in the polyester can adopt a slightly contracted conformation so that the oxygen-oxygen distance is less than in polyesters derived from p-xylylene glycol. This, together with the similar degree of rigidity and symmetry of the trans-1,4-cyclohexylene and p-phenylene ring systems, is employed to explain the observed melting points. Polyesters prepared from cis-1,4-cyclohexanedimethanol are also described. As expected from the lower degree of symmetry of the diol, these polyesters have lower melting points than the analogous compositions prepared from trans-1,4-cyclohexanedimethanol. Polyesters of cis-1,4-cyclohexanedimethanol and trimethylene glycol have similar melting points. It is suggested that a cis-1,4-cyclohexylene ring and a methylene group have a similar effect on the melting point of a polyester. Copolyesters of cis- and trans-1,4-cyclohexanedimethanol with terephthalic acid do not form a minimum melting composition. Instead, they show a continuous change of melting point from that of the polyester prepared from one stereoisomer to that of the polymer prepared from the other isomer.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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