首页> 美国卫生研究院文献>other >Clozapine Reconstructed: Haloperidol’s Ability To Reduce Alcohol Intake In The Syrian Golden Hamster Can Be Enhanced Through Noradrenergic Modulation By Desipramine And Idazoxan
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Clozapine Reconstructed: Haloperidol’s Ability To Reduce Alcohol Intake In The Syrian Golden Hamster Can Be Enhanced Through Noradrenergic Modulation By Desipramine And Idazoxan

机译:氯氮平重建:氟哌啶醇减少叙利亚黄金仓鼠中酒精摄入的能力可通过去甲肾上腺素和依达唑烷的去甲肾上腺素能调节而增强。

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摘要

BackgroundAlcohol use disorder commonly occurs in patients with schizophrenia. Most antipsychotic drugs do not lessen alcohol use; although the atypical antipsychotic clozapine has been shown to reduce alcohol use in patients with schizophrenia, its toxicity severely limits its use in patients. With an eye toward creation of a safer clozapine-like drug, we have investigated the pharmacological basis of the clozapine’s effects on alcohol drinking in the Syrian golden hamster. In this animal, as in patients with schizophrenia, clozapine reduces alcohol drinking while the typical antipsychotic haloperidol does not. We have suggested that clozapine decreases alcohol drinking due to its weak dopamine D2 receptor blockade, its potent norepinephrine α-2 receptor antagonism, as well as its ability to elevate plasma norepinephrine.
机译:背景饮酒障碍通常发生在精神分裂症患者中。大多数抗精神病药不会减少饮酒;尽管已证明非典型抗精神病药氯氮平可减少精神分裂症患者的酒精使用量,但其毒性严重限制了其在患者中的使用。为了开发一种安全的类氯氮平类药物,我们研究了氯氮平对叙利亚金仓鼠饮酒的影响的药理基础。在这种动物中,像精神分裂症患者一样,氯氮平减少了饮酒,而典型的抗精神病药物氟哌啶醇却没有。我们已经提出,氯氮平因其对多巴胺D2受体的弱阻滞作用,对去甲肾上腺素α-2受体的强效拮抗作用以及其升高血浆去甲肾上腺素的能力而减少了饮酒。

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