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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    European journal of neuroscience 8 (1996), S. 0 
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Native kainate receptors expressed by cultured hippocampal cells were studied in the whole-cell configuration of the patch-clamp technique by using a fast perfusion system. About 80% of the neurons expressed kainate receptors independently of the time in culture (0–4 days), which coincided with the number of cells immunoreactive for a monoclonal antibody against the GluR5/6/7 subunits. Three types of cells were considered: neurons in which the rapid application of kainate induced a rapidly desensitizing current, cells in which kainate induced a more slowly rising, non-desensitizing, response and those in which a mixture of both responses was apparent. Steady responses induced by 300 μM kainate were inhibited by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) in a dose-dependent manner (IC50= 0.92 μM). CNQX was less potent in blocking transient kainite-induced responses (IC50= 6.1 μM). Responses to kainate, whether steady or transient, were also inhibited by NS102, showing poor selectivity for the transient response (IC50= 4.1 and 2.2 μM respectively). The new α-amino-3-hydroxy-5-methyl-4-isoxazole (AMPA) receptor antagonist NS394 was very potent in inhibiting steady kainate-induced currents (IC50= 0.45 μM), but was even more effective in preventing peak responses (IC50= 0.13 μM). In contrast, cyclothiazide did not affect transient kainate-induced responses but did potentiate current induced by activation of AMPA receptors by AMPA or kainate. These results demonstrate the lack of complete selectivity amongst some available competitive antagonists for AMPA and kainate receptors, and indicate that kainate receptors expressed by hippocampal cells lack the cyclothiazide modulatory site present at AMPA receptors. In addition, the present data support the idea that low-affinity kainate binding sites in the brain correspond to receptor channels selectively activated by kainate.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1360-0443
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine , Psychology
    Notes: To evaluate the use of L-type calcium channel blockers (CaCB) in out-patient opiate detoxification.〈section xml:id="abs1-3"〉〈title type="main"〉DesignControlled trial with sequential allocation of patients to groups.〈section xml:id="abs1-4"〉〈title type="main"〉MethodsThree groups of individuals subject to opiate detoxification were involved: (1) the experimental group (n = 30) received a course of nimodipine and dextropropoxiphen; (2) one control group (n = 20) was detoxified with a course of dextropropoxiphen and benzodiazepine; and (3) a second control group (n = 30) was treated with a standard course of α-2-adrenergic agents and naltrexone. In all cases, the detoxification course was scheduled to last 7 days.〈section xml:id="abs1-5"〉〈title type="main"〉ResultsAll the groups showed a significant opiate withdrawal syndrome (OWS) during detoxification (follow-up effect: Λ = 0.04; F6.52 = 201.89; P 〈 0.001), but from the first day the group treated with CaCB manifested fewer symptoms than the control groups (treatment effect: F2.57 = 97.99; P 〈 0.001). From the start, the intensity of the OWS was reduced by half in the CaCB group (M = 6.67) compared with that manifested by the two other groups (M ≈ 13). The clinical impression of the evolution of the detoxification was that it was comfortable and free of complications (significant side-effects were not observed).〈section xml:id="abs1-6"〉〈title type="main"〉ConclusionsThe results of the study suggest that the use of calcium channel blockers (CaCB) may be an effective method in opiate detoxification. Full randomized trials are warranted.
    Type of Medium: Electronic Resource
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