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Chronic antipsychotic treatment exerts limited effects on the mania-like behavior of dopamine transporter knockdown mice

机译:慢性抗精神病药治疗对多巴胺转运蛋白敲低小鼠的躁狂症行为产生有限的影响

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Background: Bipolar disorder is a life-threatening disorder linked to dopamine transporter (DAT) polymorphisms, with reduced DAT levels seen in positron emission tomography and postmortem brains. Aims: The purpose of this study was to examine the effects of approved antipsychotics on DAT dysfunctionmediated mania behavior in mice. Methods: DAT knockdown mice received either D2-family receptor antagonist risperidone or asenapine and mania-related behaviors were assessed in the clinically-relevant behavioral pattern monitor to assess spontaneous exploration. Results: Chronic risperidone did not reverse mania-like behavior in DAT knockdown mice. Chronic asenapine reduced mania behavior but this effect was more pronounced in wild-type littermates than in DAT knockdown mice. Conclusion: Taken together, these findings suggest that while acute antipsychotic treatment may be beneficial in management of bipolar mania, more targeted therapeutics may be necessary for long-term treatment. Specific investigation into DAT-targeting drugs could improve future treatment of bipolar mania.
机译:背景:双相情感障碍是一种与多巴胺转运体(DAT)多态性有关的危及生命的疾病,在正电子发射断层扫描和死后大脑中可以看到DAT水平降低。目的:本研究的目的是检测经批准的抗精神病药物对小鼠DAT功能障碍介导的躁狂行为的影响。方法:对接受D2家族受体拮抗剂利培酮或阿塞那平治疗的DAT基因敲除小鼠进行临床相关行为模式监测,以评估其自发探索行为。结果:慢性利培酮不能逆转DAT基因敲除小鼠的躁狂样行为。慢性阿塞那平降低了躁狂行为,但这种效应在野生型同窝小鼠中比在DAT基因敲除小鼠中更为明显。结论:综上所述,这些发现表明,虽然急性抗精神病药物治疗可能有助于双相躁狂症的治疗,但长期治疗可能需要更多的靶向治疗。对DAT靶向药物的具体研究可以改善双相躁狂症的未来治疗。

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