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  • Chemistry  (6)
  • Theoretical, Physical and Computational Chemistry  (3)
  • Antidiuretic hormone  (2)
  • 1
    ISSN: 1432-1106
    Keywords: Antidiuretic hormone ; Osmotic stimulus ; Anteroventral third ventricular region ; Prostaglandins ; Meclofenamate ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This study explored the roles of prostaglandins in the anteroventral third ventricular region, a cerebral osmoreceptor site, in the osmoregulation mechanism of vasopressin release. We injected (1 μl) prostaglandin E2 (12.8 nmol) or meclofenamate (78.3 nmol), an inhibitor of prostaglandin biosynthesis, into the brain region or the lateral cerebral ventricle of conscious rats, examining their effects on plasma vasopressin and its controlling factors in the presence or absence of an osmotic stimulus. The injection of prostaglandin E2 into the anteroventral third ventricular region augmented plasma vasopressin and arterial pressure after 5 min and 15 min, without influencing plasma osmolality, sodium, potassium, or chloride. In contrast, intraventricular injection of prostaglandin E2 did not cause any significant effect on those variables. The i.v. infusion (0.1 ml·kg−1·min−1) of hypertonic saline (2.5 mol/l) enhanced plasma vasopressin after 15 min and 30 min; this was accompanied by increased plasma osmolality, sodium, and chloride, and by unaltered or elevated arterial pressure. Meclofenamate given into the anteroventral third ventricular region 30 min before starting the hypertonic saline infusion abolished the osmotic vasopressin response without significantly changing the responses of the other variables. Histological analysis showed that the injection sites of meclofenamate in these rats were close to those of prostaglandin E2 in the anteroventral third ventricular region and included the organum vasculosum of the lamina terminalis and the surrounding area, the medial preoptic area, and periventricular and median preoptic nuclei. When injection cannulae for meclofenamate deviated from those areas incidentally or when the drug was expressly administered into the cerebral ventricle, the osmotic vasopressin response was not inhibited. Plasma vasopressin and the other variables observed during the i.v. infusion of isotonic saline (0.15 mol/l) were not affected significantly by meclofenamate administration into the anteroventral third ventricular region or the cerebral ventricle. On the basis of these results, we concluded that prostaglandins synthesized in and/or near the anteroventral third ventricular region might contribute to the facilitation of vasopressin release in the hyperosmotic state.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Key words Anteroventral third ventricular region ; Antidiuretic hormone ; Cardiovascular regulation ; Prostaglandins ; Catecholamine receptors ; Dopamine ; Phenylephrine ; Isoproterenol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The aim of this study was to pursue the roles of the catecholamine receptors in the anteroventral third ventricular region (AV3V), a cerebral site engaged in various stress responses, in prostaglandin (PG) E2-evoked vasopressin (AVP) release and cardiovascular action. Experiments were conducted in conscious rats in which cerebral and vascular cannulae had been implanted chronically. Local infusion (0.5 µl, 1 min) of dopamine (150 nmol), a D1-dopaminergic agonist SKF 38393 (17 nmol) and an α-adrenergic agonist phenylephrine (150 nmol), as well as PGE2 (7 nmol), into the AV3V enhanced plasma AVP 5 min later, without affecting plasma osmolality and electrolytes. In contrast to the increases in both arterial pressure and heart rate observed when PGE2 was applied, dopamine and SKF 38393 did not affect these variables, and phenylephrine elevated only arterial pressure. The AV3V infusion of a β-agonist isoproterenol (100 nmol) did not change plasma AVP, although it decreased arterial pressure and increased heart rate. The increase in plasma AVP by dopamine was not blocked by the preinfusion of the D2-antagonist sulpiride (13 nmol) into the AV3V 10 min before, but was abolished by that of the D1-antagonist SCH-23390 (8 nmol). The effects of phenylephrine on both plasma AVP and the blood pressure were prevented by the preadministration of the α-antagonist phenoxybenzamine (13 nmol). However, the pretreatments with phenoxybenzamine, sulpiride or SCH 23390 did not inhibit the responses of AVP, arterial pressure and heart rate caused by PGE2. These antagonists were without significant effect on AVP and other variables when given alone. The infusion sites of PGE2 and the other drugs identified histologically included the AV3V structures such as the organum vasculosum laminae terminalis or its vicinity, median preoptic nucleus, medial preoptic nucleus and periventricular hypothalamic nucleus. Dopamine or phenylephrine administered into the cerebral ventricle at the same dose as used in the AV3V application did not exert a significant effect on plasma AVP, arterial pressure and heart rate. These results suggest that catecholamine receptors in the AV3V may not be involved in the AVP-secreting, tachycardiac and pressor responses evoked by topical action of PGE2 on this area, despite their ability to influence hormone release and cardiovascular function.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2281-2288 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethynylated polystyrene resins were prepared as functionalized polymer supports by the iodination reaction of macroporous polystyrene resins and reacted with transition metal diethynyl complex (Mt = Ni) and metal halides (Mt = Rh, Pd, and Pt) in a basic solvent using cuprous iodide as a catalyst to obtain macroporous polystyrene resins containing organotransition metals. The distribution of the metal acetylide complexes in the modified macroporous resins was determined by an electron probe microanalyzer. A gradient in the transition metal distribution was observed in any case of the modified resins. The stability of the organotransition metal complexes in the polymer matrix could be compared with a low molecular weight analogous complex quantitatively.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 2639-2647 
    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: The radiation-induced polymerization of ethylene was carried out by use of a benchscale plant with a flow-type reactor of 1 liter capacity under the following conditions: pressure, 200-400 kg/cm2; temperature, 30-90°C; irradiation intensity, 3.8 × 105 rad/hr; and ethylene flow rate, 300-3000 nl/hr. The molecular weight of polymer formed was shown to decrease with increasing reaction temperature and to increase with increasing pressure. When the ethylene flow rate increases, the molecular weight decreases in the polymerization at 30-60°C, but it does not change in the polymerization at 75-90°C. Methyl group content, which is a measure of short-chain branching of the polymer, increases with increasing reaction temperature, i.e., ca. 1 CH3/1000 CH2 at 30°C and ca. 9 CH3/1000 CH2 at 90°C. Methyl content is independent of the ethylene flow rate. The changes in the melt index of polymer with reaction conditions corresponds to the change of the molecular weight. The density, crystallinity, and melting point of polymer decrease with the reaction temperature as the short-chain branching increases, and they are almost independent of ethylene flow rate and pressure.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 70 (1998), S. 77-87 
    ISSN: 0020-7608
    Keywords: linear molecular aggregate ; coupled Liouville equation ; hyperpolarizability ; optical retarded field ; optical bistability ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We develop a numerical calculation scheme of a dynamics of the quantum network for linear molecular aggregates under time-dependent electric fields. Each molecule is assumed to be an electric dipole arranged linearly with an arbitrary angle from the longitudinal axis. This approximation is considered to be appropriate for the aggregates with large intermolecular distances and allows us to treat intermediate- and large-size aggregates without enormous direct calculations of the Coulomb interactions. The molecular interactions are taken into account by adding the radiations from these dipoles to the external electric fields. The dynamics is performed by solving the coupled Liouville equation constructed from the Liouville equation for each dipole. The effects of the retarded electric fields are evaluated with numerically exact precision by using the sixth-order Runge-Kutta scheme. As a simple example, we examine the linear aggregates involving two dipoles composed of two-state molecules under the continuous laser fields. The effects of the intensity of external fields, the intermolecular distances, and the angles between the dipole and the longitudinal axis on the population differences are investigated. The linear polarizability spectra are calculated by using the definition of nonperturbative polarizability. An abrupt change like the phase-transition behavior in the variation in the population differences for the applied field intensities is observed for the dimer models. Based on these results, we anticipate the population differences for larger (intermediate)-size aggregates.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 70: 77-87, 1998
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 70 (1998), S. 269-282 
    ISSN: 0020-7608
    Keywords: hyperpolarizability ; hydrogen chain ; bond alternation ; ab initio ; electron correlation ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ab initio calculations of the second hyperpolarizabilities (γ) for one-dimensional hydrogen chains (Hn) with different bond-length alternations and charges are performed. We investigate their signs, magnitudes, and chain-length dependences at various electron correlation levels using an extended basis set. Remarkable differences in the γ are observed for different bond-length alternations and for different charged states. In order to elucidate the differences in γ, spatial contributions of electrons to the γ are analyzed for these short and long Hn chains by using the second hyperpolarizability density plots. The effects of the introduction of charged defects into the linear chains on the γ are also investigated by varying the intercharged defects distance.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 70: 269-282, 1998
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 70 (1998), S. 659-669 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A procedure for the calculation of molecular properties in the full quantum mechanical treatment is presented. We formulate the non-Born-Oppenheimer density functional theory and propose its numerical scheme. We numerically calculate the energy, particle densities, interparticle distance, and (hyper)polarizability of the hydrogen molecule and its isotopes using this method and discuss isotope effects on the physical properties.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 70: 659-669, 1998
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 587-590 
    ISSN: 0887-6266
    Keywords: iodine-doped polystyrene ; charge-transfer (CT) complex ; XPS ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: No abstract.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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