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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 96 (1974), S. 5341-5349 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 93 (1971), S. 6004-6013 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of game theory 2 (1973), S. 129-140 
    ISSN: 1432-1270
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics , Economics
    Notes: Abstract In the present paper we defineψ-stability for theAumann-Peleg theory of cooperative games without side payments, and we prove some theorems which are analogous to the core theorem byAumann andBurger. These theorems provide foundations of the theory ofψ-stability for cooperative games without side payments in addition to being of interest for their own sake. We also consider the composition of two admissible functionsψ 1 andψ 2.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 29 (1973), S. 1094-1096 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Résumé La ligature de l'intestin, particulièrement du duodénum, gêne la sécrétion gastrique chez le Rat à pylore lié avec ou sans fistule fine.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 268 (1971), S. 125-139 
    ISSN: 1432-1912
    Keywords: Experimental Hypertension ; Norepmephrine Turnover ; Heart ; Hypothalamus ; Medulla Oblongata ; Chlorisondamine ; DOCA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In experimental hypertensive rats (DOCA-implantation, 1% saline as drinking-water, encapsulation of the left kidney), the norepinephrine turnover in peripheral sympathetically innervated organs and the central nervous system was determined either by the decay in endogenous norepinephrine after inhibition of tyrosine hydroxylase or by the ecayd in the specific norepinephrine activity after intravenous or intraventricular administration of3H-norepinephrine. In the heart, the norepinephrine turnover was accelerated in proportion to the rise in blood pressure. In hypothalamus and medulla oblongata, the turnover was delayed reciprocally to the acceleration in the heart. No changes were seen in the residual parts of the brain. Administration of chlorisondamine, a quaternary ganglionic blocking agent which does not cross the blood-brain barrier, resulted in a normalization of the increased cardiac norepinephrine turnover, whereas the changes in the brain persisted. Implantation of DOCA alone produced neither a rise in blood pressure nor changes in norepinephrine turnover. The results presented are compatible with the hypothesis that, in this form of experimental hypertension, the delay in norepinephrine turnover in the brain-stem is causally related to the increased activity of the peripheral sympathetic nervous system.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1912
    Keywords: Spontaneous Hypertension ; Norepinephrine Turnover ; Heart ; Salivary Gland ; Brain Stem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In genetically hypertensive rats, the norepinephrine turnover of peripheral and central adrenergic neurons was determined either by the decline in endogenous norepinephrine after inhibition of tyrosine hydroxylase or by the decay in the specific activity of norepinephrine after labelling the stores by intravenous or intraventricular injection of3H-norepinephrine. In the periphery (heart and submaxillary gland), the norepinephrine turnover of genetically hypertensive rats was reduced in proportion to the rise in systolic blood pressure. In the hypothalamus, medulla-pons and the residual parts of the brain, the turnover was unchanged both in the prehypertensive and the hypertensive state. The results indicate that the central adrenergic neurons, involved in the control of blood pressure, may act independently from the activity of peripheral baroreceptors. The elevated blood pressure resulting from an enhanced peripheral vascular reactivity to the physiological neurotransmitter norepinephrine may induce a compensatory inhibition of the activity of the peripheral adrenergic neurons. In the genetically hypertensive rats, neither the peripheral nor the central adrenergic nervous system seems to play a primary role in the development of hypertension.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2072
    Keywords: Intraventricular 6-Hydroxydopamine ; Increased Irritability ; Norepinephrine Turnover ; Benzodiazepines ; Neuroleptics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Intraventricular injection of 2 doses of 300 μg of 6-hydroxydopamine (6-OHDA) into rats induced an increased reactivity to exogenous (non-painful) stimuli. This increased irritability lasted more than 4 months (the longest period studied) and consisted of crying, hissing, urination, defecation, standing in an upright posture, biting and panic jumping. The degree of irritability was inversely correlated with the level of brain norepinephrine (NE). The uptake of 3H-NE into all brain regions studied was decreased after administration of 6-OHDA. The rate of 3H-NE decay from the brain stem (hypothalamus, medulla-pons) was delayed 1 week and accelerated 9 weeks after 6-OHDA administration. The decay of 3H-NE from the residual parts of the brain was enhanced both 1 and 9 weeks after 6-OHDA injection. Diazepam, chlordiazepoxide and meprobamate suppressed the increased irritability at doses which did not cause muscle relaxation. The normalization of the behavior produced by diazepam was accompanied by a normalization of the rate of 3H-NE decay both in the brain stem and the residual parts of the brain. The neuroleptics chlorpromazine and haloperidol were effective in abolishing the increased irritability only at strongly sedative doses.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2072
    Keywords: Morphine-6-Hydroxydopamine ; Analgesia ; Brain Catecholamines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract One week following the intraventricular administration on successive days of two doses of 6-hydroxydopamine (6-OHDA) (0.1–1 mg/kg) to rats, the norepinephrine (NE) and dopamine (DA) contents in the brain were markedly decreased. These treatments potentiated the effect of morphine on the tail-flick latency after intraperitoneal or intraventricular administration of morphine. The intraventricular administration of two doses of 6-OHDA (0.5 mg/ kg) did not change the morphine concentrations in brain or plasma, or the duration of pentobarbital anesthesia. After 6-OHDA (total=20 Μg) had been injected bilaterally into the medial hypothalamic areas at the level of the ventromedial or dorsomedial hypothalamic nuclei, or into the medial forebrain bundle, morphine analgesia was also potentiated and there was marked reduction of the hypothalamic NE levels. The administration of high doses (2 mg/kg) of 6-OHDA into the lateral ventricles decreased the enhanced morphine analgesia and markedly depleted the brain NE and dopamine concentrations. The administration bilaterally of 6-OHDA (total=20 Μg) into caudatus-putamen areas reduced morphine analgesia. In conclusion, 6-OHDA induced depletion of NE content in the hypothalamus potentiates morphine analgesia, whereas depletion of DA in the caudate nucleus decreases morphine analgesia.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 13 (1974), S. 54-59 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 615-623 
    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: Crystallization during melt spinning is studied as an example of the nonisothermal crystallization of polymers. The following equation is derived, taking the temperature distribution within a filament into consideration: \documentclass{article}\pagestyle{empty}\begin{document}$$ \kappa \nabla ^2 T = {\rm V} \cdot {\rm grad } \ T - \frac{{\Delta H}}{{C_p }}{\rm V} \cdot {\rm grad } \ X $$\end{document} where T = temperature, X = crystallinity, κ = thermal diffusivity, V = velocity, ΔH = heat of crystallization, and Cp = specific heat at constant pressure. The assumptions and the procedure for a numerical calculation of crystallinity and temperature within a running filament are described, and some results of calculation are illustrated. The results are compared with those obtained by a simpler calculation in which the radial temperature distribution is neglected. The simpler method proved useful in connection with x-ray measurements.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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