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奥氮平:姑息医学的最新进展。

Olanzapine: palliative medicine update.

作者信息

Prommer Eric

机构信息

Mayo Clinic Arizona, Phoenix, AZ 85054, USA.

出版信息

Am J Hosp Palliat Care. 2013 Feb;30(1):75-82. doi: 10.1177/1049909112441241. Epub 2012 Apr 10.

Abstract

Olanzapine is an atypical antipsychotic agent of the thienobenzodiazepine class. Olanzapine blocks multiple neurotransmitter receptors, including dopaminergic (D(1), D(2), D(3), and D(4)), serotonergic (5-hydroxytryptamine 2A [5-HT(2A)], 5-HT(2C), 5-HT(3), and 5-HT(6)), adrenergic (α(1)), histaminic (H(1)), and muscarinic (M(1), M(2), M(3), and M(4)) receptors. Olanzapine has a high affinity for the 5HT(2A) receptor, which is up to 5 times greater than the dopamine receptor, resulting in less propensity to the development of extrapyramidal side effects. The affinity of olanzapine for multiple receptors has lead to the identification of olanzapine as an important agent in the treatment of delirium, nausea, and vomiting. Olanzapine has been demonstrated to have opioid-sparing properties. Olanzapine is principally metabolized by glucuronidation, with a smaller metabolic contribution from the cytochrome oxidase system. Adverse effects of olanzapine include somnolence, postural hypotension, constipation, dizziness, restlessness, and weight gain. The purpose of this article is to outline the pharmacodynamics, pharmacology, and evidence for the use of olanzapine in palliative care.

摘要

奥氮平是一种噻吩并苯二氮䓬类非典型抗精神病药物。奥氮平可阻断多种神经递质受体,包括多巴胺能受体(D(1)、D(2)、D(3)和D(4))、5-羟色胺能受体(5-羟色胺2A [5-HT(2A)]、5-HT(2C)、5-HT(3)和5-HT(6))、肾上腺素能受体(α(1))、组胺能受体(H(1))和毒蕈碱能受体(M(1)、M(2)、M(3)和M(4))。奥氮平对5HT(2A)受体具有高亲和力,其亲和力比多巴胺受体高5倍,导致锥体外系副作用的发生倾向较低。奥氮平对多种受体的亲和力已使其被认定为治疗谵妄、恶心和呕吐的重要药物。奥氮平已被证明具有节省阿片类药物的特性。奥氮平主要通过葡萄糖醛酸化代谢,细胞色素氧化酶系统的代谢贡献较小。奥氮平的不良反应包括嗜睡、体位性低血压、便秘、头晕、烦躁不安和体重增加。本文的目的是概述奥氮平在姑息治疗中的药效学、药理学及应用证据。

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