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  • 1
    ISSN: 1432-0428
    Keywords: Fetal gastrointestinal epithelium ; insulin receptors ; rat fetus ; quantitative autoradiograph
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Purified carrier-free 125I-insulin was injected into the vitelline vein of rat fetuses in utero after 17, 19 or 21 days of a 22-day gestation. Three minutes later, the weight and radioactivity of various organs and the remaining carcass were measured. A radioactivity concentration index was calculated by dividing the specific activity of each organ by that of the whole feto-placental unit. In each of the three age groups studied, the gastrointestinal tract radioactivity concentration indices were 1.7, 2 and 1.9 respectively, indicating that the gastrointestinal tract concentrated the labelled hormone. Three, 9 and 15 min after 125I-insulin injection, the gastrointestinal tract was removed, homogenized and chromatographed on a G-50 fine Sephadex column. At 3 min, 91.4% of gastrointestinal tract radioactivity co-eluted with a standard of 125I-insulin. At the later time intervals studied, the percentage of 125I-insulin decreased while that of low molecular weight degradation products increased. Quantitative autoradiographic study of the fetal gastrointestinal tract indicated that epithelial cells bound 125I-insulin and that this binding was inhibited by co-injection of large amounts of unlabelled insulin. 125I-insulin binding was highest in the proximal small bowel and lowest in the colon. Insulin binding did not appear to depend upon degree of cell maturation or cell type. These results indicate that the epithelium of the gastrointestinal tract is characterized by the presence of numerous insulin receptors and is a potentially important insulin target.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 20 (1981), S. 563-567 
    ISSN: 1432-0428
    Keywords: Rat fetus ; feto-placental units ; placental extract ; glucose ; amino acids ; non esterified fatty acids ; insulin ; glucagon ; corticosterone ; isolated islets ; placento-insular axis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rat pups delivered by caesarian section one day before term, either remained attached to (experimental group) or were separated from their placenta (control group). Both groups were transferred into an incubator and their metabolic parameters studied. In the control group, plasma amino acid concentration fell from 11.2 to 6.9 mmol/l, plasma insulin fell from 151 to 45 μU/ml and blood glucose fell from 3.5 to 2.6 mmol/l during the first hour of extrauterine life. In the breathing feto-placental units, plasma amino acid concentration remained at its birth level, plasma insulin remained high (109 μU/ ml) causing rapid hypoglycaemia (1.63 mmol/l). An immediately postnatal glucagon and corticosterone surge was visible only in the experimental group. A partially purified placental extract (molecular weight 6000 to 30000) stimulated insulin secretion in vivo (fasted adult rats) and in vitro (isolated neonatal islets). It is concluded that the placenta maintains fetal hyperinsulinaemia by creating fetal hyperaminoacidaemia and, possibly, by secreting a beta cytotropic factor.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 26 (1970), S. 759-760 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Zusammenfassung Eine hochmolekulare Verbindung wurde aus Exudaten von Granulombeuteln von Ratten gereinigt. Diese Substanz, i.p. an Ratten verabreicht, hemmt das durch Kaolin oder durch Carrageenin erzeugte Pfotenoedem, nicht dagegen das durch Histamin, Serotonin oder Polyvinylpyrrolidon erzeugte Oedem.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 22 (1976), S. 463-465 
    ISSN: 1432-0827
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Clinica Chimica Acta 73 (1976), S. 481-486 
    ISSN: 0009-8981
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Inorganic Biochemistry 16 (1982), S. 245-252 
    ISSN: 0162-0134
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical & experimental allergy 23 (1993), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Effect of eetirizine. a potent and specific H1 receptor antagonist, was examined on platelet activating factor-induced bronchoconstrietion in 10 patients (5 male, mean [s.e.m.] aged 37 4 [3–6] years) with mild asthma in a placebo controlled, double-blind cross-over study. Airway responses were assessed by measuring specific airway conductance (SGaw). Patients were challenged with a single dose (12–96 μG) of PAF that had previously produced a 35% fall in SGaw. PAF challenges were performed after single dose (15 mg) and I week's treatment (15mg twice daily) of cetirizine. There was no significant difference in pre-and post-treatment baseline values of SGaw on different study days and the percentage changes after cetirizine were 38 7 (701) and 45–6 (5–52) eompared to 50 2 (2–89) and 43–9 (7–26) with placebo respectively. Similarly mean (s.e.m.) area under eurve (AUC-SGaw/time course response) was 391 (143) and 514 (85) with cetirizine compared to 565 (37) and 461 (94) with placebo respectively. The difference was not statistically significant. There was no difference in facial flushing and feeling of warmth between cetirizine and placebo. We conclude that PAF induced bronehoconstriction in humans is not mediated by histamine release and that H1 receptor antagonists do not modify PAF indueed bronehoeonstriction.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical & experimental allergy 23 (1993), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Cetirizine is a potent, selective H1 histamine receptor antagonist. The effect of oral and inhaled eetirizine was assessed on the early bronchoconstrictor response to inhaled allergen in 10 mild atopie asthmatic patients in a double-blind, randomized, plaeebo controlled trial. All were sensitive to Dermatophagoides pleronyssinus and this was used as the provoking allergen. The geometric mean PD20 FEV] values obtained at allergen challenge were measured as cumulative breath units (c.b.u.) and following oral cetirizine, inhaled cetirizine and placebo were 124–5, 75–7 and 76–7 c.b.u. respectively. These did not differ significantly. We conclude that neither oral nor inhaled cetirizine significantly attenuates the early response to inhaled allergen in atopie asthmatic subjects. However, the method of repeated allergen challenge is likely to be relatively insensitive. Clinical and Experimental Allergy, [o]. 23, pp. 528–531.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The effect of a single dose of prednisolone (20 mg) or cetirizine (10 mg) on the immunohistology of the cutaneous late-phase reaction was determined in a double-blind, placebo-controlled, cross-over study in 12 atopic allergic individuals. The subjects were challenged with intradermal allergen (30 BU) 2 hr after ingestion of the drugs or placebo. The magnitude of the cutaneous reactions were determined at 15 min, 6 and 24 hr, and skin biopsies performed at 24 hr. Cetirizine produced a 50% average inhibition of the immediate weal and flare response (P=0.001) and a 27% average inhibition of the 6 hr late-phase induration (NS). Prednisolone reduced the immediate (27%, P=0.03) and significantly inhibited the late-phase reaction (53%, P=0.02). Prednisolone significantly inhibited infiltration of CD45+ (total leucocytes), neutrophil elastase+, EG2+ (activated eosinophils) and CD25+ (IL-2R) cells (P=0.017, 0.005, 0.005 and 0.032 respectively). CD3, CD4, CD8 and HLA-DR expression was also inhibited but this was not significant. Cetirizine also reduced the numbers of EG2+ cells, particularly those with high counts before treatment but the overall results were not significant. No other changes in the cellular infiltrate were demonstrated when cetirizine was compared with placebo. These findings indicate a single dose of prednisolone significantly reduces leucocyte infiltration and activation as well as the magnitude of the cutaneous late-phase reaction.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background Cetirizine is a non-sedating H1 antihistamine which is effective in the treatment of allergic rhinitis and urticaria. It inhibits eosinophil and basophil chemotaxis in late cutaneous allergic reactions in skin windows. Its effect on early (EAR) and late asthmatic reactions (LAR) is less certain.Methods We examined the effect on EAR and LAR of 3 days treatment with oral cetirizine (15mg twice daily) compared with a single dose of inhaled beclomethasone 10min prior to allergen challenge in a placebo-controlled (oral and inhaled) doubleblind cross-over design with three treatment arms separated by 14 days.Results Cetirizine did not significantly inhibit either the EAR or LAR documented by maximum percentage fall in FEV1 (0-3 and 6-9h) or as area under the curve (AUC between 0 and 3 and 6–9 h), Beclomethasone inhibited the LAR compared with placebo (P = 0.02) when expressed as AUC (6–9h). This did not quite reach statistical significance (P = 0.06) when expressed as maximal percentage late fall in FEV1 between 6 and 9h. A greater than twofold increase in airways responsiveness to methacholine was observed 3h after challenge which was significantly reduced by beclomethasone compared with placebo (P 〈 0.02) and cetirizine (P 〈 0.05). The data suggest that oral cetirizine does not significantly inhibit either the EAR or LAR. Beclomethasone inhibited both the early increase in airways responsiveness and the subsequent LAR. Our study also confirms the view that early increases in airway responsiveness precede the late response and suggests that these associated events are not dissociable by the pharmacological treatments employed in this study.
    Type of Medium: Electronic Resource
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