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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Pharmacology 9 (1969), S. 119-134 
    ISSN: 0362-1642
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 202 (1964), S. 1222-1223 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In the acute spinal cat DOPA inhibits transmission from the flexor reflex afferents (FRA) to primary afferents, motoneurones and ascending pathways6. Further experiment shows that 5-HTP has a similar effect. After intravenous injection of 50-100 mg/kg 5-HTP (DL form) there is a decrease or ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 202 (1964), S. 1344-1345 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1. The records illustrate two experiments on the effect of DOPA on discharges in muscle efferents (A-D) and on dorsal root potentials (E and F). A, C and E were obtained before and J3, Z〉 and F 10 min after intravenous injection of DOPA. The lower traces in A-D are efferent discharges in ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Psychiatric Research 11 (1974), S. 97-104 
    ISSN: 0022-3956
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 43 (1978), S. 11-17 
    ISSN: 1435-1463
    Keywords: noradrenaline receptor ; clonidine ; circulatory changes ; flexor reflex activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of the central noradrenaline receptor stimulating agent clonidine on blood pressure, heart rate, and flexor reflex activity were studied in intact rats and in rats chronically treated with ethanol. The clonidine-induced changes were similar in ethanol-treated animals and in animals never subjected to ethanol. The results suggest that the sensitivity of central noradrenaline receptors involved in the mediation of the circulatory changes and of the flexor reflex activity after clonidine is not altered by chronic administration of ethanol.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 47 (1980), S. 175-180 
    ISSN: 1435-1463
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Metiamide (800μg intracerebroventricularly to rats) enhanced the DOPA accumulation in noradrenaline-predominant brain areas following DOPA decarboxylase inhibition and it accelerated theα-methyltyrosine-induced disappearance of noradrenaline in the brain, both normally and after clonidine (0.1 mg/kg i.p.). These findings indicate that metiamide stimulates the release of noradrenaline. They can explain why metiamide antagonizes the clonidine-induced hypotension.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 61 (1985), S. 21-34 
    ISSN: 1435-1463
    Keywords: GABA ; amino acids ; rat brain ; acute and chronic hemisection ; nerve impulse flow ; glutamic acid decarboxylase inhibitors ; GABA transaminase inhibitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The concentrations of GABA, glutamate, serine, glutamine, threonine, glycine and taurine in the substantia nigra and in the corpus striatum of the rat were determined electrochemically following condensation with o-phthalaldehyde-β-mercaptoethanol and reverse-phase, high performance liquid chromatography. After a frontal hemisection at the level of the caudal hypothalamus, the GABA concentration in the substantia nigra on the operated side decreased to about 20 per cent of the normal value in 4 days, in all probability caused by degeneration of the nerve terminals of the striato-nigral GABA neurons. The concentrations of taurine in the substantia nigra and of GABA in the corpus striatum were initially lowered and later elevated following this lesion. The concentration of glutamate in the substantia nigra was lower on the sectioned side and higher on the intact side at 14 days as compared to 4 hours after a hemisection. Following an acute hemisection, the GABA transaminase inhibitorγ-acetylenic GABA increased the concentration of GABA by 36 % and 79 % in the substantia nigra on the sectioned and intact side, respectively. The glutamate decarboxylase inhibitors 4-deoxypyridoxine and isoniazid lowered the concentration of GABA in the substantia nigra by about 50% on both the sectioned and intact side. The results indicate that the synthesis, but not the utilization of GABA in the substantia nigra is dependent on the normal nerve impulse flow. The concentration of glutamine was changed in directions contrary to that of GABA following a chronic hemisection or treatment withγ-acetylenic GABA, in agreement with the suggestion that glutamine is a precursor of the GABA transmitter pool.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1435-1463
    Keywords: Noradrenaline ; dopamine ; cell body region ; axon terminals ; nerve impulses ; synthesis ; utilization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The nerve impulse flow to the noradrenaline nerve cell body region of the superior cervical ganglion and to the noradrenaline nerve terminals of the salivary glands was decreased and increased by decentralization and preganglionic electrical stimulation, respectively. The concentrations of dopamine, noradrenaline, and their primary deaminated metabolites (DOPAC, DOPEG) in the ganglion were not changed during the first day after the decentralization but were increased following preganglionic stimulation, particularly that of DOPAC. The disappearances of dopamine and noradrenaline afterα-methyltyrosine and the disappearance of noradrenaline after inhibition of the dopamine-β-hydroxylase were not changed by decentralization or stimulation. The accumulation of dopamine following inhibition of the dopamine-β-hydroxylase was somewhat lowered by decentralization and was markedly enhanced by stimulation. In the noradrenaline nerve terminals of the salivary glands, preganglionic sympathetic stimulation decreased and increased the concentration of noradrenaline and dopamine, respectively. Thus, nerve impulses stimulated the tyrosine hydroxylase activity in the cell body region and the axon terminals of the noradrenaline neurons but they increased the utilization of noradrenaline only in the terminals.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 33 (1972), S. 211-222 
    ISSN: 1435-1463
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Treatment with the monoamine oxidase inhibitor nialamide (500 mg/kg i.p., 2.5 and 5 h) produced in the caudal and cranial half of the spinal cord an increase in 5-hydroxytryptamine which was of the same magnitude in intact rats and in rats acutely spinalized midthoracically. Similar results were obtained after reserpine pretreatment. The nialamide-induced increase in 5-hydroxytryptamine caudal to a transection was slightly reduced after 2 days and completely inhibited after 3 weeks. Treatment with the tryptophan hydroxylase inhibitorp-chlorophenylalanine (319 mg/kg i.p., 24 h) or its methylester HCl (400 mg/kg i.p., 24 h) reduced the concentration of 5-hydroxytryptamine in the spinal cord by about 70 per cent in both halves of the intact cord and in the cranial half of the cut cord but by only about 30 per cent caudal to an acute transection. The nialamide-induced increase in 5-hydroxytryptamine of a transected spinal cord was inhibited to the same extent cranial and caudal to the lesion 24 h after treatment withp-chlorophenylalanine. In conclusion, the changes in 5-hydroxytryptamine concentrations induced byp-chlorophenylalanine are dependent on nerve impulses in contrast to those induced by nialamide. Thep-chlorophenylalanine does not have to be incorporated into newly synthesized tryptophan hydroxylase in order to inhibit the enzyme.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 34 (1973), S. 93-100 
    ISSN: 1435-1463
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of the dopamine-β-hydroxylase inhibitor bis-(4-methyl-1-homopiperazinylthiocarbonyl)-disulphide (FLA-63) on the release of dopamine and noradrenaline was studied in regions of the rat central nervous system rich in dopamine or noradrenaline nerve terminals. The release was investigated by analyzing the accumulation of the 3-0-methylated catecholamines after inhibition of the monoamine oxidase by nialamide. In the dopamine-rich corpus striatum, the concentration of dopamine was unchanged but its release was enhanced after treatment with FLA-63. The noradrenaline concentration and release were markedly reduced. In the areas containing mainly noradrenaline nerve terminals, dopamine accumulated but did not stoichiometrically replace the missing noradrenaline. There was a pronounced release of dopamine from the noradrenaline nerves after the dopamine-β-hydroxylase inhibiticn. This release may, at least partly, explain why noradrenaline is not stoichiometrically replaced by dopamine.
    Type of Medium: Electronic Resource
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