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  • Dopamine  (171)
  • Springer  (171)
  • 1980-1984  (171)
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  • Springer  (171)
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  • 1
    ISSN: 1435-1463
    Keywords: Dopamine ; N-methyl-4-phenyl-l, 2, 3, 6-tetrahydropyridine ; mice ; 3-methoxytyramine ; motor activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The acute effects of N-methyl-4-phenyl-l, 2, 3, 6-tetrahydropyridine (NMPTP) on mouse central monoaminergic neurons were investigated. In striatum, two hours after the injection of NMPTP (50 mg/kg s.c.) there was a seven-fold increase in 3-methoxytyramine that coincided with a 55 % decrease in dopamine. In addition, the same dose of NMPTP caused an acute increase in mouse motor activity; this effect was antagonized by haloperidol or by pretreatment with reserpine. These data indicate that NMPTP initially causes a pronounced release of dopamine into the extraneuronal space.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 57 (1983), S. 129-137 
    ISSN: 1435-1463
    Keywords: Dopamine ; autoreceptors ; agonist ; antagonist ; utilization ; rat brain regions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Theα-methyltyrosine-induced disappearance of dopamine was inhibited by the selective dopamine autoreceptor agonist B-HT 920 in the corpus striatum, the nucleus accumbens, the olfactory tubercle, the limbic cortex, and the rostral part of the cerebral cortex of the rat. These inhibitory actions of B-HT 920 were almost completely reversed by the dopamine receptor antagonist haloperidol, indicating that they were caused by a stimulation of dopamine autoreceptors. In the caudal cortex and the cerebellum, the effects of B-HT 920 and haloperidol were less clear, perhaps due to a low concentration of dopamine and to the occurrence of this dopamine in both dopamine and noradrenaline neurons. In the hypothalamus, B-HT 920 and haloperidol did not change theα-methyltyrosine-induced disappearance of dopamine in agreement with previous findings that the tubero-infundibular dopamine neurons are not regulated via dopamine receptors.
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  • 3
    ISSN: 1435-1463
    Keywords: Dopamine ; autoreceptors ; rat brain regions ; B-HT 920 ; gammabutyrolactone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Following interruption of the nerve impulse flow in the dopamine neurons by treatment with gammabutyrolactone, the selective dopamine autoreceptor agonist B-HT 920 reduced the DOPA accumulation after DOPA decarboxylase inhibition and the 3,4-dihydroxyphenylacetic acid concentration in the corpus striatum, the nucleus accumbens, the olfactory tubercle, the limbic cortex and the rostral part of the cerebral cortex of rats. The effects were completely inhibited by the dopamine receptor antagonist haloperidol, indicating that they were caused by stimulation of dopamine autoreceptors. In the caudal part of the cerebral cortex and the cerebellum, B-HT 920 somewhat reduced the concentration of dihydroxyphenylacetic acid via a haloperidol-sensitive mechanism, suggesting that there are a few dopamine neurons with autoreceptors in these regions. No evidence was obtained for the presence of autoreceptors on the dopamine neurons in the hypothalamus. The gammabutyrolactone-induced elevation of the dopamine concentration was not reduced by B-HT 920 in any region, suggesting that this effect of gammabutyrolactone was caused by decreased release rather than increased synthesis of dopamine under our experimental circumstances.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 50 (1981), S. 179-184 
    ISSN: 1435-1463
    Keywords: Dopamine ; cyclic AMP ; anterior pituitary
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Effects of different concentrations of dopamine on the cyclic AMP concentration in the rat anterior pituitary gland were investigated in vitro. Low concentrations of dopamine (10−9–10−8 mol/l) were found to decrease, whereas the high concentration (10−5 mol/l) increased the cyclic AMP concentration in pituitaries collected from ovariectomized and estradiol-treated females. In contrast, dopamine had no effect on the anterior pituitary cAMP concentration when pituitaries were collected from ovariectomized rats which had not received estrogen replacement. These data show that the action of dopamine on the anterior pituitary cAMP largely depends on the dopamine concentration and the hormonal state of animals.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 314 (1980), S. 177-182 
    ISSN: 1432-1912
    Keywords: Dopamine ; Renal vasodilation ; Metoclopramide ; Competitive antagonism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The interaction of metoclopramide with renal dopamine receptors has been characterized in anesthetized dogs surgically prepared with arterial blood pressure catheters and renal artery blood flowprobes. In normal dogs, i. v. dopamine (3 μg/kg) produced consistent and selective decrements in renal vascular resistance (RVR) and increments in renal blood flow over a 220 min test period; mean arterial blood pressure and cardiac rate were minimally affected. Pretreatment with metoclopramide, 1 and 10 mg/kg i. v., resulted in dose-related inhibition (maximum inhibition 44% and 94%, respectively) of the renal vasodilator activity of dopamine without altering baseline parameters. The duration of antagonism produced by 1 mg/kg of metoclopramide was approximately 30 min, while 10 mg/kg resulted in significant attenuation for the entire test period. Decreases in RVR produced by prostaglandin A1 (0.03 and 0.3 μg/kg, i. v.) and bradykinin (3 and 15 μg/kg, i. v.) that were comparable to those of dopamine were unaltered by metoclopramide. Furthermore, metoclopramide did not affect the diastolic blood pressure responses to noradrenaline (0.1–3 μg/kg, i. v.) or isoproterenol (0.03–0.3 μg/kg, i. v.), nor did it alter dopamine-induced vasoconstriction of the iliac vasculature. In phenoxybenzamine (3 mg/kg, i. v.) treated dogs, dopamine (0.3–30 μg/kg, i. v.) produced dose-related reductions in RVR. Administration of metoclopramide (10 mg/kg, i. v.) resulted in a 10-fold parallel displacement, to the right, of the RVR dose-response curve to dopamine. These findings demonstrate that metoclopramide is an effective antagonist of renal dopamine receptors following systemic administration in the dog. The results are not consistent with the classification of metoclopramide as a selective antagonist of D-2 receptors.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of gynecology and obstetrics 233 (1983), S. 259-262 
    ISSN: 1432-0711
    Keywords: Dopamine ; Uterine blood flow ; Placental insufficiency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The systemic and uterine hemodynamic effects of dopamine were studied in six near-term pregnant Texel sheep. Dopamine was administered by i.v. infusion in doses ranging from 2 to 16 μg per kilogram per minute. After administration of 2 and 4 μg/kg/min, Dopamine produced a statistically significant increase in uterine blood flow (p 〈 0.02). The mean value of the increase was 68.3 ml/min. When doses of 8 and 16 μg/kg/min were given, the responses were variable. Systolic and diastolic arterial pressure remained unchanged up to dopamine dosages of 8 μg/kg/min. Heart rate also showed no significant increase but a trend in this direction was seen. Low-dosages of dopamine could be used in the treatment of patients with placental insufficiency.
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  • 7
    ISSN: 1432-0827
    Keywords: Isoproterenol ; Dopamine ; Propranolol ; PTH ; Calcitonin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Available evidencein vitro andin vivo suggests that pharmacologic doses of isoproterenol stimulate the secretion of parathyroid hormone (PTH) and calcitonin (CT) and propranolol inhibits secretion. However, the findings in man are either quite modest or inconsistent. In view of this controversy, we examined the effects of isoproterenol, 0.15 µg intradermally (i.d.), dopamine, 5 µg/kg body weight over 60 min intravenously (i.v.), and propranolol, 1 mg over 5 min followed by 60 µg per min for 2 i.v. in normal human subjects. It was found that these agents did not alter serum calcium, serum immunoreactive PTH, or plasma immunoreactive CT. The findings do not support a physiologic role for biogenic amines in the control and regulation of PTH or CT secretion in normal man.
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  • 8
    ISSN: 1432-2072
    Keywords: Cyclazocine ; Acute treatment ; Dopamine ; Noradrenaline ; Serotonin ; Monoamine metabolites ; Brain regional assay ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of cyclazocine on the metabolism of dopamine (DA), noradrenaline (NA) and 5-hydroxytryptamine (5-HT) in regions of rat brain were studied by measuring changes in the levels of the monoamines and their major metabolites. Doses ranging from 4–32 mg/kg were tested. Rats were sacrificed 1 or 2 h after administration of the drug, according to the experiment. Administration of cyclazocine significantly decreased DA concentration and increased the levels of DOPAC and HVA in striatum. Cyclazocine decreased the levels of NA, and markedly increased the levels of MHPG-SO4 and 5-HIAA in cortex, hypothalamus, midbrain and pons-medulla, while little change in 5-HT concentration, except a decrease after the highest dose, was observed. These changes in the metabolism of the monoamines differed in their amplitude and temporal nature. The possible roles of dopaminergic, noradrenergic and serotoninergic neurons in different brain regions are discussed in relation to modifications of locomotor activity and the induction of bizarre behavior resulting from cyclazocine administration in rats. These investigations may add to the understanding of the mechanism of psychotomimetic effects produced in man by this drug.
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  • 9
    ISSN: 1432-2072
    Keywords: Ethanol tolerance ; Serotonin ; Norepinephrine ; Dopamine ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats were permanently depleted of brain dopamine (DA), serotonin (5-HT), 5-HT+norepinephrine (NE), or NE +DA by intraventricular injection of either 5,7-dihydroxytryptamine (5,7-DHT) or 6-hydroxydopamine (6-OHDA) with or without pretreatment with desmethylimipramine (DMI). Following 1 week of recovery from surgery, daily treatment with ethanol (5 g/kg, PO) or isocaloric sucrose was carried out for a period of 20–25 days. Testing at 5-day intervals showed that chronic ethanol treatment produced tolerance to the hypothermic and motor impairing effects of ethanol. Depletion of 5-HT alone retarded tolerance, while depletion of NE or DA alone produced no effect. Combined depletion of both NE and 5-HT, however, completely inhibited tolerance development. The inhibition of tolerance development by combined depletion of both NE and 5-HT is dicussed in terms of a reciprocal relationship between these two systems.
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  • 10
    ISSN: 1432-2072
    Keywords: Conditioned avoidance response ; α-Methyl-p-tyrosine ; Suppression ; Dopamine ; Reversal ; Nucleus accumbens
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract These experiments sought to determine whether dopamine (DA) could reverse the depressive effects of α-methyl-p-tyrosine (AMPT) on a conditioned avoidance response (CAR). Rats were randomly allocated to shocked groups (CAR-trained) and non-shocked (CAR-naive) groups. The CAR-trained rats, conditioned to avoid an electric shock, were administered AMPT (150 mg/kg at-24 h and 50 mg/kg at-1 h, both IP), nialamide (80 mg/kg IP at-1 h) and saline (1 μl) or DA (5 or 10 μg/μl, dissolved in 1 μl saline, at time 0) directly into the nucleus accumbens. The rats were then tested for CAR at 0.5, 1, 2, 3, 4, 8, 12, 24 and 48 h. The CAR-naive rats, conditioned to the behavioural environment without electric shock being presented, were administered AMPT, nialamide and DA or saline as above. Both doses of DA antagonised the AMPT-induced suppression of the CAR in the CAR-trained rats, reaching a maximum 2–4 h after its local application. In the CAR-naive rats, DA produced a ‘pseudo-CAR’ that lasted about 4 h, but which completely disappeared at 8 h when the DA effect had worn off. These CAR-naive rats did not learn a CAR under the influence of DA. In a third group of rats, DA produced locomotor activation which, in its time course, resembled the effect of DA on CAR. It is concluded that the ability of DA to antagonise AMPT-induced depression of CAR is, in all likelihood, dependent upon DA-induced locomotor excitation, rather than upon an effect of DA on associative learning.
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