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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 84 (1991), S. 211-220 
    ISSN: 1435-1463
    Keywords: Competitive NMDA-antagonists (SDZ EAA-494, CGP 37849) ; dopamine agonists (CI 201-678, SDZ 205-152) ; glutamate ; dopamine ; locomotion ; mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The competitive NMDA-antagonists SDZ EAA-494 and CGP 37849 and the mixed D-1/D-2 dopamine agonists CI 201-678 and SDZ 205-152 reverse akinesia in monoamine-depleted mice in a dose dependent manner. Combination of threshold doses of NMDA-antagonists with dopamine agonists markedly enhances anti-akinetic effects. CI 201-678 which in addition to D-1 and D-2 receptors stimulates α-2 receptors produces a stronger effect than SDZ 205-152 which is devoid of α-2 agonist activity. The results indicate that concomitant blockade of NMDA-receptors and activation of dopamine receptors results in synergistic or at least additive motor stimulatory effects.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-0879
    Keywords: cAMP ; Calcium metabolism ; Parathyroid hormone ; Ion-exchanger ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rats received a diet containing a Cabinding ion exchanger at a dose of 30 and 90 g/kg diet, respectively. Following 10 days of oral administration there was a dose dependent increase in urinary cAMP excretion. However, after 20 days treatment the measured cAMP content in the urine was no longer different from control values. The results suggest that urinary cAMP excretion in the rat is only of value as an indication of acute changes in PTH-activity.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 325 (1984), S. 17-24 
    ISSN: 1432-1912
    Keywords: Cyclic AMP ; Noradrenaline release ; Cerebral noradrenaline neurones ; Forskolin ; Phosphodiesterase inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The role of adenosine 3′,5′-cyclic monophosphate (cAMP) in the release of noradrenaline from central neurones has been investigated by examining the effects of forskolin, 3-isobutyl-1-methylxanthine (IBMX), cis-6-(p-acetamidophenyl)-1,2,3,4,4a,10b-hexahydro-8,9-dimethoxy-2-methylbenzo[c] [1,6]-naphthyridine bis (hydrogenmaleinate) (AH21-132; a new phosphodiesterase inhibitor) and N6, O2′-dibutyryl-adenosine 3′,5′-cyclic monophosphate (dibutyryl-cAMP) on the outflow of tritiated compounds from rat and rabbit cerebral cortex slices preincubated with [3H]-noradrenaline. Forskolin, IBMX, AH21-132 and dibutyryl-cAMP produced a concentration-dependent increase in both basal and electrically-evoked efflux of tritium from rat and rabbit cortex slices. The increase in basal tritium efflux from rabbit cortex slices elicited by forskolin and IBMX could be attributed mainly to an increase in [3H]-DOPEG although a small increase in [3H]-noradrenaline was also observed. Forskolin and (when combined with noradrenaline) IBMX and AH21-132 increased the cAMP content of rat cortex slices at similar or somewhat higher concentrations that they increased tritium efflux. Neither forskolin nor IBMX or AH21-132 had any effect on the cocaine-sensitive uptake of [3H]-noradrenaline into synaptosomes prepared from rat or rabbit cortex. The effects of forskolin, IBMX and dibutyryl-cAMP on electrically-evoked overflow of tritium from rat and rabbit cortex slices were reduced when cocaine (10 μM) was present in the superfusion medium, although forskolin produced a similar increase in cAMP in the absence or presence of cocaine. It is suggested that cAMP may facilitate the normal process of noradrenaline release by nerve stimulation.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1435-1463
    Keywords: SDZ PSD 958 ; D1 receptor antagonist ; catalepsy ; rearing ; stereotypy ; locomotion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary SDZ PSD 958, a novel benzo[g]quinoxaline derivative exhibits the properties of a potent orally active selective D1 receptor antagonist. It has high affinity for D1-like receptors (D1, D5; pKi=9.7–9.8) labelled by [3H]SCH23390 and is at least 400 fold less active at D2-like receptors (i.e. D2, D4) labelled by [3H]spiperone. Effects in functional tests are consistent with d1 receptor antagonist properties. SDZ PSD 958 inhibited apomorphine-induced rearing in mice and prevented prolongation of novelty-induced locomotion in rats elicited by the selective D1 receptor agonist CY 208-243. By contrast, SDZ PSD 958 did not induce catalepsy and only weakly inhibited apomorphine-induced stereotyped gnawing in rats. This suggests that SDZ PSD 958 preferentially inhibits responses mediated by dopamine systems innervating the limbic system.
    Type of Medium: Electronic Resource
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