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氯丙嗪后胆碱能反弹加重锂诱导的大鼠边缘系统毒蕈碱样癫痫发作:对精神科治疗的启示

Cholinergic rebound after chlorpromazine exacerbates lithium muscarinic-induced limbic seizures in rats: implications for psychiatric treatment.

作者信息

Bureau Y R, Persinger M A

机构信息

Laurentian University, Sudbury, Ontario, Canada.

出版信息

Psychol Rep. 1991 Aug;69(1):171-6. doi: 10.2466/pr0.1991.69.1.171.

Abstract

When lithium serum levels were within the (human) therapeutic range, young and old adult male and female rats (housed singly or in groups) all displayed faster limbic seizure onset times in response to a muscarinic cholinergic agonist (pilocarpine 20 mg/kg) if a single systemic dosage of chlorpromazine was injected 24 hours previously. The effect was comparable to injecting an additional 10 mg/kg of pilocarpine. These results strongly suggest that cholinergic rebound from chlorpromazine administrations during lithium treatment could facilitate subclinical electrical lability and very localized neuronal necrosis within the limbic system of clinical patients, resulting in normalization of psychiatric symptoms.

摘要

当锂血清水平处于(人类)治疗范围内时,如果在24小时前单次全身注射氯丙嗪,无论年轻或年老的成年雄性和雌性大鼠(单独或成组饲养)在给予毒蕈碱胆碱能激动剂(毛果芸香碱20mg/kg)后,边缘系统癫痫发作的起始时间均会加快。这种效应与额外注射10mg/kg毛果芸香碱相当。这些结果强烈表明,锂治疗期间氯丙嗪给药引起的胆碱能反弹可能会促进临床患者边缘系统内亚临床电不稳定和非常局部的神经元坏死,从而导致精神症状的正常化。

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