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左美丙嗪在人脑的受体结合情况——对难治性精神分裂症治疗的启示

Levomepromazine receptor binding profile in human brain--implications for treatment-resistant schizophrenia.

作者信息

Lal S, Nair N P, Cecyre D, Quirion R

机构信息

McGill Center for Research in Schizophrenia, Douglas Hospital, Verdun, Quebec, Canada.

出版信息

Acta Psychiatr Scand. 1993 Jun;87(6):380-3. doi: 10.1111/j.1600-0447.1993.tb03391.x.

Abstract

The receptor binding profile of levomepromazine (LMP) in human brain was compared with that of clozapine (CLOZ) and chlorpromazine (CPZ). LMP showed significantly greater binding affinity for both alpha-1 and serotonin-2 binding sites than either CLOZ or CPZ, and significantly greater binding to alpha-2 sites than CPZ. A potent pharmacological effect at these receptor sites may explain the beneficial effect of LMP on psychotic symptoms and akathisia in treatment-resistant schizophrenia recently described in 2 open studies. LMP requires further appraisal as a potentially useful neuroleptic in the management of treatment-resistant schizophrenia.

摘要

将左美丙嗪(LMP)在人脑中的受体结合情况与氯氮平(CLOZ)和氯丙嗪(CPZ)进行了比较。LMP对α-1和血清素-2结合位点的结合亲和力显著高于CLOZ或CPZ,且对α-2位点的结合显著高于CPZ。在这些受体位点产生的强效药理作用可能解释了LMP对难治性精神分裂症的精神病性症状和静坐不能的有益作用,这在最近两项开放研究中已有描述。LMP作为难治性精神分裂症治疗中一种潜在有用的抗精神病药物,需要进一步评估。

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