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  • Caudate nucleus  (1)
  • Key words Bremazocine  (1)
  • Sarcoidosis  (1)
  • 1
    ISSN: 1432-1912
    Keywords: Acetylcholine-release ; Caudate nucleus ; Dopamine-receptor ; Receptorsupersensitivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of a number of dopamine-receptor agonists on depolarization-induced (26 mM K+) release of 3H-acetylcholine from slices of rat caudate nucleus were examined with a superfusion method. Apomorphine (10−6 M) and N,N-dipropyliso-ADTN (10−7 M) inhibited acetylcholine-release in vitro by about 50% and these inhibitory effects were antagonized by haloperidol. For N,N-dipropyl-iso-ADTN an EC50 of approximately 3×10−9 M was estimated from its dose-response curve. However, dopamine (10−6 M) itself and bromocriptine (10−6 M) inhibited acetylcholine-release less. Presumably: the weak effect of exogenous dopamine is due to its (partial) uptake in dopaminergic nerve terminals and to the fact that released endogenous dopamine already partially activates the receptors involved in the inhibition of acetylcholine-release. Pretreatment of young rats with 6-hydroxydopamine (+ desipramine) increased the inhibitory effects of dopamine-receptor agonists, including dopamine itself, on acetylcholine-release from caudate slices, indicating dopamine-receptor supersensitivity. This was corroborated by the finding that apomorphine-induced stereotyped behavior was significantly higher in rats lesioned with 6-hydroxydopamine than in controls. It is suggested that K+-induced release of radiolabelled acetylcholine from caudate nucleus slices provides a functional model to study the characteristics of post-synaptic dopamine-receptors in vitro. The concentrations of dopamine-receptor agonists needed to inhibit acetylcholine-release appear to be in the nanomolar range, in agreement with their affinities as determined in dopamine-receptor binding studies. In contrast, these concentrations are much lower than those required for stimulation of dopamine-sensitive adenylate cyclase activity.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: Key words Bremazocine ; U50 ; 488H ; Naltrexone ; Ethanol ; Sucrose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract It has been postulated that opioid systems in the brain may play a role in ethanol reinforcement. In this respect, μ- and δ-opioid receptors may mediate the rewarding effects whereas κ receptors are thought to mediate the aversive effects of opioids. Accordingly, long-acting benzomorphans such as bremazocine, that simultaneously act as μ and δ receptor antagonists and κ receptor agonists may be particularly effective in reducing ethanol self-administration. Therefore, we studied the effect of bremazocine on oral ethanol self-administration in rats using a paradigm [unrestricted free-choice drinking of 10% (v/v) ethanol], previously shown to cause long-term neuroadaptations in the nucleus accumbens and caudate putamen. Bremazocine (0.1 mg/kg, once daily for five consecutive days) reduced ethanol drinking by about 50% during the active period of the animals, whereas the intake of sucrose (3–10% w/v) was affected neither in naive nor in ethanol-experienced rats. This effect of bremazocine appeared not to be secondary to its acute sedative effect or the slight increase in total fluid consumption. Unlike bremazocine, the selective κ-opioid receptor agonist U50,488H (10 mg/kg, once daily) inhibited ethanol drinking only during the first of 5 treatment days and the opioid receptor antagonist naltrexone (0.3–10 mg/kg, once daily) only caused a modest (about 20%) suppression of ethanol drinking during the first hours after drug injection. Thus, bremazocine appears to be far more potent than the clinically applied drug naltrexone in this respect. Our data further support the role of opioid receptors in ethanol reinforcement and indicate that long-acting mixed-action opioids such as bremazocine may be useful as adjuvants for the clinical management of ethanol addiction.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1619-7089
    Keywords: Scintigraphy ; Somatostatin ; Sarcoidosis ; Tuberculosis ; Wegener's granulomatosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Normal as well as activated lymphocytes and macrophages have previously been shown by radioreceptor analysis to express somatostatin receptors (SS-R). The somatostatin (SS) analogue [111In-DTPA-d-Phe1]octreotide (111In-octreotide) is already used successfully in the visualization of a variety of neuro-endocrine tumours and malignant lymphomas. In the present study 20 consecutive patients were investigated, 12 with sarcoidosis, one with both sarcoidosis and aspergillosis, four with tuberculosis and three with Wegener's granulomatosis. For in vivo SS-R imaging, total-body scintigraphy was performed 24 and 48 h after the administration of 111In-octreotide. Granuloma localizations could be visualized in all patients studied; additional sites were found in nine patients with sarcoidosis and in two patients with tuberculosis. In vitro autoradiography of fresh tissue biopsies, using the SS analogue [125I-Tyr3]octreotide, showed binding at sites that were microscopically identified as granulomatous inflammation. These observations demonstrate the expression of SS-R by human granulomas. This scintigraphy procedure may contribute to a more precise staging and evaluation of granulomatous diseases, but more importantly it may be a sensitive indicator of the efficacy of glucocorticoid and/or immunosuppressive therapy.
    Type of Medium: Electronic Resource
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