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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 5171-5180 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The configuration statistics for a macromolecule that is sandwiched between and either repelled or adsorbed by a pair of plane parallel surfaces are developed by means of a generating function technique. The theory is based on our previous work [J. Chem. Phys. 85, 5299 (1986)] on the problem of a single plane; it has the advantages of simplicity and flexibility. The generating functions that are constructed are used to evaluate expectation values for the lengths of loops, bridges, and tails as well as the number of bound segments. The canonical partition function for a molecule of n lattice steps is extracted from the generating function by use of numerical integration.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 5299-5305 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The problem of a macromolecule adsorbed on a single surface is treated by means of a generating function technique. The basic method has the virtues of simplicity and flexibility. The statistical weights that appear in the generating functions for tails, trains, and loops can be calculated with use of a variety of models. The essential physics of the adsorption process, and the occurrence of a critical point, are transparent in this treatment. Illustrative calculations are done for the simplest case, in which tails have unit weight, trains have binding energies proportional to their lengths, and loops are weighted by lattice walk statistics. Methods for treating more realistic models for chains, and for handling their interactions when there is multiple chain adsorption, are discussed.
    Materialart: Digitale Medien
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  • 3
    facet.materialart.
    Unbekannt
    London : Periodicals Archive Online (PAO)
    Medical History. 12 (1968) 385 
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  • 4
    facet.materialart.
    Unbekannt
    Terre Haute, Ind. : Periodicals Archive Online (PAO)
    Contemporary Education. 40:6 (1969:May) 321 
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Journal of algebraic combinatorics 1 (1992), S. 5-5 
    ISSN: 1572-9192
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Mathematik
    Materialart: Digitale Medien
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  • 6
    ISSN: 1432-1912
    Schlagwort(e): Bromocriptine ; Dopamine autoreceptors ; Dopamine D1 receptors ; Dopamine D2 receptors ; Motor depression ; Motor stimulation ; Single cell recording ; Substantia nigra pars compacta
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Bromocriptine (BRC) produced a biphasic behavioural effect in mice; an early depressant phase which lasted for about 1 h and a later stimulant phase which lasted from about 1 to 5 h. The stimulation was blocked with SCH23390. Both phases of activity were accompanied by marked striatal DA autoreceptor effects as indicated by reductions in dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) levels and by a reduction in the accumulation of DOPA (after inhibition of nigrostriatal DA nerve firing and DOPA decarboxylase). However, while the autoreceptor effects were still evident during the behavioural stimulant phase, there was a gradual rise in DOPAC and HVA from 1 to 4 h after injection, indicating a gradually increasing DA turnover. We were unable, using a variety of behavioural and biochemical paradigms, to demonstrate any change in DA autoreceptor sensitivity after one dose of BRC. In electrophysiological studies, however, it was found that prior exposure of rats to one dose of BRC rendered them subsensitive to the rate-inhibiting effects of a second dose of BRC, as measured in anaesthetized animals using extracellular single cell recordings of identified DA neurons in the substantia nigra pars compacta. It is concluded firstly, that the stimulant phase of BRC in mice occurs despite continued occupation of the DA autoreceptors by BRC because adequate endogenous DA is available to provide the required D1 receptor stimulation and secondly, that the terminal autoreceptors in the striatum (as assessed in mice using biochemical techniques) may be regulated differently to the somatodendritic autoreceptors (as assessed electrophysiologically in rats).
    Materialart: Digitale Medien
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  • 7
    ISSN: 1432-1912
    Schlagwort(e): Bromocriptine ; Dopamine autoreceptors ; Dopamine D1 receptors ; Dopamine D2 receptors ; Motor depression ; Motor stimulation ; Dialysis Neurotransmitter
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The aim of the present study was to further investigate the behavioural and biochemical pharmacology of the directly acting dopamine (DA) receptor agonist bromocriptine (BRC). BRC produced an initial depression of locomotion followed after about an hour by a weak but significant locomotor stimulation. The stimulation was potentiated by concomitant administration of the D1 agonist SKF38393. Ex vivo biochemical determinations indicated that reductions in dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) levels occurred in the striatum after BRC injection without a significant change in DA levels, indicating a reduced DA turnover. An increase in 5-hydroxytryptamine (5HT) and 5-hydroxyindoleacetic acid (5HIAA) levels occurred in the striatum leading to a significant increase in turnover (i.e. ratio of 5HIAA to 5HT). Noradrenaline concentrations increased in the striatum. In the cortex, sharp falls in HVA and DOPAC levels without a corresponding change in DA were observed. While there was no significant change in noradrenaline levels in this brain region, an increase in 5HIAA, but not in 5HT, levels occurred. These changes indicate an increase in 5HT turnover (ratio of 5HIAA to 5HT). In vivo dialysis indicated that extracellular levels of DA, DOPAC and HVA in the striata of freely moving rats were sharply reduced for at least 6 h after injection. In vitro binding studies showed that BRC exhibited high (Ki values in low nanomolar range) affinities for DA D2A, D2B, D3, α1 and α2 adrenergic receptors together with unexpectedly high affinity (about 1 nM) for 5HT1A receptors. The data indicate that the initial behavioural depression and later locomotor stimulation induced by BRC are accompanied by a sharp monophasic fall in striatal extracellular DA levels as indicated by dialysis studies. Since the behavioural stimulation was augmented by concomitant D1 receptor stimulation, the data suggest that the reduced DA turnover is influencing the amount of DA available to stimulate postsynaptic D1 receptors. However, the biochemical studies indicated that BRC has a high affinity for 5HT1A receptors and affects the turnover of 5HT in the brain. Thus, the behavioural effects of BRC may depend not only on effects on the DA system but also on 5HT systems.[/p]
    Materialart: Digitale Medien
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  • 8
    ISSN: 1432-2072
    Schlagwort(e): d-Amphetamine ; Supersensitivity ; Nucleus accumbens ; Apomorphine ; Chronic
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Treatment of rats with d-amphetamine (5 mg/kg) once daily for 25 days did not change locomotor responses, on day 7 of withdrawal, to dopamine (DA) or d-amphetamine into the nucleus accumbens. Nor was there a change in 3H-spiperone binding of caudate nucleus membranes. There was no effect of treatment on the locomotor response of rats to 1.0, 1.5 or 2.0 mg/kg d-amphetamine IP. However, d-amphetamine-treated rats were significantly less sensitive to 0.5 mg d-amphetamine. Although 1, 2 or 3 mg/kg apomorphine produced the same degree of stereotypy in both treatment groups, there was a significant difference in the response of the two groups to 0.5 mg apomorphine, d-amphetamine-treated animals being less sensitive than vehicle-treated animals. No change was found in brain DA levels with or without synthesis inhibition. The present data do not support the hypothesis that chronic treatment of rats with d-amphetamine can produce supersensitive post-synaptic DA receptors.
    Materialart: Digitale Medien
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  • 9
    ISSN: 1432-2072
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 340 (1989), S. 6-12 
    ISSN: 1432-1912
    Schlagwort(e): Dopamine D-2 receptors ; In vivo binding ; Mouse ; Raclopride ; Striatum
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The kinetic properties of the accumulation of 3H-raclopride, a selective dopamine (DA) D-2 receptor antagonist, in mouse striatum in vivo was examined under various experimental conditions. The accumulation in striatum was saturable in contrast to that in cerebellum, which linearily increased with the dose. The specific binding of 3-Hraclopride in the striatum, defined as the difference in the accumulation in striatum and cerebellum 30 min after the injection was completely inhibited by the D-2 receptor antagonists spiperone and (-I-)-butaclamol [but not (−)butaclamol] and the DA receptor agonist N-n-propylnorapomorphine. The mean B max value of the specific binding was 40.7 ± 2.8 pmol/g tissue and the mean apparent K D value, based on the dose injected, was 87.8 ± 11.5 nmol/kg i. v. (18 different experiments). Pretreatment of the mice with a single injection of reserpine 4 h or 3 days beforehand reduced the apparent K D value which in part seemed to be due to the decreased concentration of synaptic DA. Similarly, γ-butyrolactone injected immediately before raclopride reduced the apparent KD value, whereas amfonelic acid and (−)-amphetamine increased the observed K D values. These findings indicate competition between endogenous DA and raclopride for the D-2 receptors. Both reserpine and γ-butyrolactone increased the apparent B max value by about 50% which indicates a receptor pool of DA for which raclopride does not compete.
    Materialart: Digitale Medien
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