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监测抗精神病药物的血浆浓度。

Monitoring plasma concentrations of neuroleptics.

作者信息

Lader M

出版信息

Pharmakopsychiatr Neuropsychopharmakol. 1976 Jul;9(4):170-7. doi: 10.1055/s-0028-1094491.

Abstract

Among the neuroleptics chlorpromazine has been the most extensively studied despite its complex metabolic pathways. Several metabolites, in particular 7-hydroxychlorpromazine, are psychotropically active. Oral phenothiazines are extensively metabolised "first-pass" through the liver. The relationship between clinical response and plasma concentrations of neuroleptics is tenous. The reasons for the lack of correlation include spontaneous remission in some patients, problems with flexible dosage schedules, the type of patient studied, differences in metabolic patterns, induction of metabolism in the liver, interactions with other drugs, and variations in plasma protein binding. Alternative research strategies might be to study metabolically less complex drugs such as haloperidol or to relate clinical response to autonomic, extrapyramidal, EEG, biochemical or endocrine measures.

摘要

在抗精神病药物中,尽管氯丙嗪的代谢途径复杂,但它仍是研究最为广泛的药物。它有几种代谢产物,尤其是7-羟基氯丙嗪,具有精神活性。口服吩噻嗪类药物在肝脏中会经历广泛的“首过”代谢。抗精神病药物的临床反应与血浆浓度之间的关系并不紧密。缺乏相关性的原因包括一些患者的自发缓解、灵活给药方案的问题、所研究患者的类型、代谢模式的差异、肝脏代谢的诱导、与其他药物的相互作用以及血浆蛋白结合的变化。替代的研究策略可能是研究代谢复杂性较低的药物,如氟哌啶醇,或者将临床反应与自主神经、锥体外系、脑电图、生化或内分泌指标联系起来。

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