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长期使用左旋多巴无法减轻长期使用氟哌啶醇后自我刺激的反弹增强现象。

Chronic l-dopa fails to lessen rebound enhancement of self-stimulation after chronic haloperidol.

作者信息

Rose I C, Mintz M, Herberg L J

机构信息

Institute of Neurology, Queen Square, London, England.

出版信息

Pharmacol Biochem Behav. 1988 Jul;30(3):585-8. doi: 10.1016/0091-3057(88)90069-x.

Abstract

Chronic treatment with haloperidol (approximately 4.8 mg/rat/day PO for 18 days) severely impaired variable-interval hypothalamic self-stimulation. Cessation of treatment was followed by a strong rebound increase in response rates at submaximal currents, to well above pretreatment rates. The rebound increase in responding was not prevented (and at submaximal currents was actually enhanced) by treatment with l-dopa plus benserazide (respectively 240 and 60 mg/kg/day PO) for 6 days after withdrawal of haloperidol. This result is at variance with previously reported findings.

摘要

用氟哌啶醇进行长期治疗(约4.8毫克/大鼠/天,口服,持续18天)严重损害了可变间隔下丘脑自我刺激。停止治疗后,在次最大电流下反应率出现强烈的反弹增加,远高于治疗前的水平。在停用氟哌啶醇后用左旋多巴加苄丝肼(分别为240和60毫克/千克/天,口服)治疗6天,并没有阻止反应的反弹增加(在次最大电流下实际上还增强了)。这一结果与先前报道的发现不一致。

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