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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 280 (1973), S. 363-371 
    ISSN: 1432-1912
    Keywords: Dopamine ; Cardiovascular Action ; Desipramine ; 6-Hydroxydopamine ; Reserpine ; Indirect Mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In rats anaesthetized with urethane the pressor effect of dopamine was not significantly altered by treatment with desipramine, which enhanced the action of noradrenaline on blood pressure and heart rate and abolished that of tyramine. Chemical sympathectomy with 6-hydroxydopamine in rats potentiated responses to noradrenaline and prevented the action of tyramine on blood pressure but did not significantly modify the pressor effects of dopamine. Furthermore, pretreatment with reserpine shifted the dose-response curves for dopamine and for tyramine on heart rate to the right. The dose-response curve for dopamine like that for noradrenaline on blood pressure was unaltered or shifted slightly to the left by reserpine. It is concluded that also in the rat an indirect, tyramine-like component contributes substantially to the cardiovascular action of dopamine.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 284 (1974), S. 1-13 
    ISSN: 1432-1912
    Keywords: 6-Hydroxydopamine ; Chemical Sympathectomy ; Spontaneous Hypertension ; Adrenergic Nervous System
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In order to evaluate the role of the sympathetic nervous system in the development and maintenance of spontaneous hypertension, spontaneously hypertensive and normotensive rats were give 6-hydroxydopamine (6-OH-dopamine). A single i.v. dose of 6-OH-dopamine (100 mg/kg) caused a biphasic rise in blood pressure in both hypertensive and normotensive rats. During long-term treatment the first dose of 6-OH-dopamine (25 or 50 mg/kg i.v.) lowered the blood pressure, measured 24 h after injection, two or three times more in hypertensive than in normotensive rats. As a result, the blood pressure reached the same level in both groups, i.e. 90–100 mm Hg. Within three days this hypotension subsided. After repeated weekly administration of 6-OH-dopamine the depressor effect declined gradually and after 4 weeks it was no longer significant. When this stage was reached, adrenal demedullation as such neither lowered the basal blood pressure, nor prevented the development of tolerance to 6-OH-dopamine. Accordingly, the adrenal medulla is not decisive in maintaining the blood pressure and in the development of tolerance to the depressor effect of 6-OH-dopamine in spontaneously hypertensive and normotensive animals. After treatment with 8 weekly doses of 6-OH-dopamine, the pressor response to noradrenaline increased in both hypertensive and normotensive rats, while the response to tyramine decreased. When, on the second day after birth, new-born rats of the hypertensive strain were given a single dose of 6-OH-dopamine (50 mg/kg i.p.) the development of hypertension was inhibited to some degree. This inhibition was more marked when the animals were given weekly doses of 6-OH-dopamine (50 mg/kg i.p.) during 5 weeks. On the other hand, when pregnant rats of the same strain received 6-OH-dopamine (50 mg/kg i.v.) twice during the last week before delivery, the offsprings did develop hypertension. It is evident that the adrenergic nervous system plays an important part in the development of hypertension in rats of a spontaneously hypertensive strain, but it is no longer of essential importance once the hypertension is established.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 284 (1974), S. 115-131 
    ISSN: 1432-1912
    Keywords: Dopamine ; l-dopa ; 6-Hydroxydopamine ; Metabolic Effects ; Adrenoceptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In male rats some metabolic effects of l-dopa and dopamine were compared with those of noradrenaline, adrenaline and tyramine by measuring the changes of plasma free fatty acids (FFA), plasma glycerol and plasma glucose as well as those of blood lactate and blood pyruvate. After intravenous injection of dopamine lactate and pyruvate concentrations were elevated maximally already within 5 min and returned to control levels after 10–20 min, i.e. at a time, when the levels of FFA, glycerol and glucose were maximally elevated in plasma. l-dopa had about 1/8 to 1/6 the potency of dopamine in producing these metabolic effects. The effects of dopamine were similar to those obtained with 1/20 the dose of noradrenaline, while adrenaline produced a more pronounced hyperglycaemic response than dopamine did when given in lipolytically equieffective doses. Pretreatment of the animals with phentolamine completely prevented the hyperglycaemic response to dopamine or noradrenaline without clearcut effects on the lipolytic effect of these catecholamines. Also, pretreatment with dihydroergotamine antagonized the hyperglycaemic effect of adrenaline and prevented that of dopamine and noradrenaline, while the effect of catecholamines on plasma glycerol concentration was not affected. However, the elevation in plasma FFA level induced by catecholamines was clearly antagonized by dihydroergotamine. The β-adrenolytic drug Kö 592 had no effect on the hyperglycaemic effect of dopamine or noradrenaline, but antagonized the lipolytic effect of these amines. Pargyline enhanced the elevation of FFA and glycerol induced by dopamine or noradrenaline but reduced their hyperglycaemic effect. Chemical sympathectomy induced by pretreatment with 6-hydroxydopamine prevented the hyperglycaemic and lipolytic effects of tyramine, antagonized those of dopamine and potentiated the lipolytic response to noradrenaline. The effect of syrosingopine on the metabolic responses to the catecholamines was similar to that of 6-hydroxydopamine. Since the metabolic effects of dopamine were clearly antagonized by various α- and β-receptor-blocking agents and by chemical sympathectomy, we conclude that dopamine exerts its metabolic effects through a stimulation of α- and β-adrenoceptors and that part of this effect is mediated by a tyramine-like action of dopamine.
    Type of Medium: Electronic Resource
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