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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 27 (1984), S. 375-377 
    ISSN: 1432-1041
    Keywords: sulpiride ; TRH ; PRL unresponsiveness
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The mechanisms of prolactin (PRL) unresponsiveness to repeated sulpiride (SUL) injections were investigated in 7 normal males. The experimental protocol consisted of two phases, separated by a 5 day interval. In both phases the administration of 1 mg/kg i. m. of SUL was followed 24 hours later, by the administration of the same dose of SUL together with either placebo (PL, 2 ml saline i. v.) or TRH (200 mcg i. v.). A control TRH test (200 mcg i. v.) was also performed. PRL showed a significant increase after the administration of SUL alone in both phases. Twenty-four hours later plasma PRL was still higher than the basal level and it was not significantly modified by administration of SUL+PL, or by SUL+TRH. The data seem to show that the lack of responsiveness of PRL to repeated administration of SUL is not due to refractoriness of dopaminergic receptors but probably to exhaustion of the hypophyseal PRL pool.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-7241
    Keywords: naloxone ; captopril ; hypertensives ; blood pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary It has been reported that naloxone, an opiate receptor antagonist, blunts the hypotensive effect of captopril in normotensives. However, our previous data did not show any interaction between captopril given acutely and naloxone (0.1 mg/kg) in hypertensives. To test whether a greater naloxone dose could interfere with the hemodynamic effect of chronically administered captopril, 12 male hypertensives were studied: Six of them had been under captopril treatment (50 mg tid) for at least 1 month, whereas the others had been drug free for the same time. Both groups randomly received a saline or naloxone (0.2 mg/kg) infusion for 1 hour, and blood pressure, heart rate, PRA, plasma aldosterone, adrenaline, and noradrenaline were measured at regular intervals before, during, and after naloxone infusion. In drug-free hypertensives, naloxone tended to reduce blood pressure slightly and did not modify heart rate, PRA, plasma aldosterone, adrenaline, or noradrenaline. In captopril-treated hypertensives, naloxone did not blunt the hypotensive effect of captopril, but rather enhanced it, without changing the heart rate, adrenaline, and noradrenaline. Moreover, naloxone increased the renin-stimulating action and did not modify the aldosterone-inhibiting effect of captopril. Our results show that the hemodynamic action of captopril given chronically is not influenced by opioid receptor blockade and therefore that the antihypertensive effect of this drug seems to be unrelated to the activation of the opioidergic system.
    Type of Medium: Electronic Resource
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