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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 144 (1967), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 178 (1956), S. 981-981 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] For this purpose we had to synthesize carbon-14 -curarine of the highest possible radioactivity by methylation of 2.0 mgm. nor-curarine with an excess of 6.4 mgm. 14CH3I, having the activity of 1 me. After recrystallization we obtained 0-25 mgm. pure carbon-14 - curarine - iodide (biquaternary) ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 86 (1985), S. 270-273 
    ISSN: 1432-2072
    Keywords: Hashish extract ; Δ 9-Tetrahydrocannabinol ; Social learning model ; Submissive behavior ; Retention deficit ; State dependency ; Analgesia ; C3H mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of hashish extract on adaptive behavior of male mice were studied in a paradigm which allows the investigation of learning mechanisms in a social context. Mice of the C3H strain, which were not submissive in a confrontation with a nonaggressive DBA mouse on day 1, were defeated on day 2 over 3 min by aggressive, isolated DBA mice, and showed conditioned submissive behavior upon mere contact with a nonaggressive DBA mouse on day 3. A hashish extract containing 38.6–39.4% Δ 9-tetrahydrocannabinol (Δ 9-THC), 11.6–12.0% cannabinol and 47.7–48.5% cannabidiol was administered orally in all experiments. Hashish extract given 90 min before defeat on day 2, in dosages corresponding to 1, 5, and 10 mg Δ 9-THC/kg, impaired retention of defensive upright, defensive sideways and immobility on day 3 (experiment 1). Experiment 2 showed that the drug (5, and 10 mg Δ 9-THC/kg) had no antinociceptive potency in mice and did not modify defeat-induced analgesia. Experiment 3, with drug (5 mg Δ 9-THC/kg) or solvent administration on day 2 and day 3, showed that the retention deficit was neither due to state-dependent learning, nor to impaired retrieval. It is suggested that hashish extract administered before learning may interfere with memory processing.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1912
    Keywords: 14C-Toxiferine ; Nicotinic acetylcholine receptor ; Motor endplate ; Endplate potential ; Autoradiography ; Saturation of drug binding sites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. To study the quantitative correlation between the stabilizing effect of toxiferine on the postsynaptic membrane and the number of drug binding sites at the motor endplate, experiments were performed on isolated mouse hemidiaphragms using combined electrophysiological and autoradiographic techniques. 2. The membrane stabilizing effect of 14C-toxiferine was investigated over a wide range of concentrations, in order to obtain not only muscle paralysis but the complete abolition of the endplate response to nerve stimulation. 3. Motor endplate activity was recorded intracellularly. For each concentration of the drug the percentage of endplates reacting to nerve stimulation with action potentials (a.p.), or with subliminal endplate potentials (e.p.p.), or being completely blocked, was determined. The mean amplitude of the e.p.p.'s was also calculated. 4. Reduction of the e.p.p. to an undetectable level required a concentration of 14C-toxiferine about 3 times greater than that which induced complete paralysis. 5. Correlation of these data with autoradiographic measurements demonstrated that decreasing e.p.p. amplitude corresponded to increasing values for the number of drug binding sites per endplate. Saturation was reached by that concentration which completely blocked the postsynaptic sensitivity to ACh. 6. It is concluded that at this concentration all the specific drug binding sites are occupied.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 294 (1976), S. 61-68 
    ISSN: 1432-1912
    Keywords: p-Nitrophenyl diazonium fluoroborate ; Cholinergic neurons ; Acetylcholine receptor ; Acetylcholinesterase ; Affinity labelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Electrophysiological experiments were done to investigate the effect of p-nitrophenyl diazonium fluoroborate (p-NPD) on motor endplates of the frog's m. cutaneus pectoris. The compound has no direct depolarizing effect on the postsynaptic membrane and stabilizes it irreversibly when added to the bath. Longtime iontophoretical applications of p-NPD produce a biphasic effect: initially a potentiation of the depolarizations due to acetylcholine (ACh) (both iontophoretically applied and presynaptically liberated), and subsequently an inhibition of the response to ACh. When the acetylcholinesterase (AChE) is inactivated previously, only the inhibiting effect of the compound is demonstrable. The association constant of p-NPD to purified AChE and to membrane fragments of electroplax was determined by biochemical methods. The compound's affinity to the AChE was found to be about 20 times greater than to the acetylcholine receptor (AChR). Iontophoretical application of p-NPD to cholinergic neurons in the hippocampal cortex of the cat also produced the characteristic biphasic effect on ACh-induced activity of these investigated neurons. The results suggest that the biphasic effect depends on the capacity of p-NPD to combine with both the AChE and the AChR. The AChE is first inhibited with low concentrations thereby potentiating the ACh response. At higher concentrations the AChR's are progressively inhibited too, thereby diminishing the excitability of the postsynaptic membrane up to a complete block.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 305 (1978), S. 143-148 
    ISSN: 1432-1912
    Keywords: Serotonin ; Serotonin receptor ; p-Chlorophenylalanine ; Motor activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of p-chlorophenylalanine (PCPA) on the specific binding of 3H-serotonin (5-HT) was investigated in crude membrane preparations of the rat forebrain. The level of cerebral 5-HT and 5-hydroxyindoleacetic acid were concomitantly determined. A single dose of PCPA (300 mg/kg i.p.) increased specific binding at a low concentration of 3H-5-HT within 24 h by more than 100%. The timecourse of the elevation of specific binding was mirrored by the reduction in the 5-HT level. However, 8–10 days after drug administration, specific binding was close to the control level, while 5-HT was still significantly reduced. A Scatchard analysis revealed that the apparent affinity was significantly increased (k D reduced) during the initial period after PCPA administration, whereas the number of binding sites (B Max) was little changed. In contrast, after repeated injections of PCPA (3 injections of 300 mg/kg at 6–8 day intervals, or 100 mg/kg/day for up to 12 days) leading to a prolonged 5-HT depletion, B Max was significantly increased, while k D tended to be restored towards the baseline level. Daily injections of PCPA (100 mg/kg) for 12 days resulted in a transitory increase in day-time motor activity with a maximum on drug day 3, and in a persistent reduction of night-time activity. It is concluded that the initial PCPA-induced decrease in k D was due to a reduced competition for binding sites by the endogenous 5-HT, whereas the increase of B Max after a prolonged 5-HT depletion may reflect a 5-HT receptor supersensitivity.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 266 (1970), S. 101-112 
    ISSN: 1432-1912
    Keywords: Muscle Endplate ; Denervation ; Acetylcholinesterase ; Decamethonium ; Oholinergic Receptor ; Muskelendplatte ; Denervation ; Acetylcholinesterase ; Decamethonium ; cholinergischer Receptor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Using contact-autoradiography of the whole mouse diaphragm, the distribution of14C-labelled decamethonium during the degeneration of the phrenic nerve was investigated, and compared with cholinesterase staining. Four days after denervation uniform radioactivity is found over the whole muscle which is independent of the duration of the denervation, whereas in the control (right half of the diaphragm with intact phrenic nerve) the radioactivity remains concentrated in the endplate area. The distribution of the radioactivity is independent of the cholinesterase concentration. Quantitative densitometer measurements give a higher molecule count per endplate for decamethonium than for curare, which corresponds with the diffuse distribution of the cholinergic receptors in the endplate region.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 42 (1964), S. 51-58 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 31 (1975), S. 1107-1108 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Zusammenfassung Ein Elektrodensystem wird beschrieben, um kleinere und grössere Teile des Elektro-Organs vonTorpedo marmorata direkt in vitro stimulieren und ableiten zu können.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 205 (1965), S. 1190-1191 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] AUTORADIOGRAPHIC methods have not yet found /JL application to thin-layer chromatography of 3H-labelled compounds because of the low tritium energy (Emax = 18-5 keV; Emean = 5-7 keV). The tritium range in a layer of sodium-o-(carboxymethyl) cellulose and in sodium alginate has been determined by ...
    Type of Medium: Electronic Resource
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