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新型抗精神病化合物的药理特性。

Pharmacological properties of new neuroleptic compounds.

作者信息

Coscia L, Causa P, Giuliani E, Nunziata A

出版信息

Arzneimittelforschung. 1975 Sep;25(9):1436-42.

PMID:25
Abstract

RMI 61 140, RMI 61 144 and RMI 61 280 are newly synthetized N-[8-R-dibenzo(b,f)oxepin-10-yl]-N'-methyl-piperazine-maleates which show interesting psychopharmacologic effects. This work contains the results of a study performed with these three compounds, in order to demonstrate their neuropsycholeptic activity in comparison with chloropromazine (CPZ) and chlordiazepoxide (CPD). The inhibition of motility observed in mice shows that the compounds reduce the normal spontaneous motility as well as the muscle tone. The central-depressant activity is evidenced by increased barbiturate-induced sleep and a remarkable eyelid ptosis can also be observed. Our compounds do not show any activity on electroshock just as do CPZ and CPD. As to the antipsychotic outline, our compounds show strong reduction of lethality due to amphetamine in grouped mice and a strong antiapomorphine activity. They show also an antiaggressive effect and an inhibitory activity on avoidance behaviour much stronger than CPZ. We have also found extrapyramidal effects, as catalepsy, common to many tranquillizers of the kind of the standards used by us. As for vegetative phenomena, the compounds show hypotensive dose related action ranging from moderate to strong, probably due to an a-receptor inhibition. Adrenolytic activity against lethal doses of adrenaline, antiserotonin and antihistaminic effects, as well as other actions (hypothermia, analgesia, etc.) confirm that RMI 61 140, RMI 61 144 and RMI 61 280 are endowed with pharmacologic properties similar and more potent than those of CPZ. Studies on the metabolism of brain catecholamines show that they are similar to CPZ, although with less effect on dopamine level.

摘要

RMI 61 140、RMI 61 144和RMI 61 280是新合成的N-[8-R-二苯并(b,f)氧杂卓-10-基]-N'-甲基-哌嗪马来酸盐,具有有趣的精神药理作用。这项工作包含了对这三种化合物进行研究的结果,以便与氯丙嗪(CPZ)和氯氮卓(CPD)相比,证明它们的抗精神病活性。在小鼠中观察到的运动抑制表明,这些化合物降低了正常的自发运动以及肌张力。巴比妥酸盐诱导的睡眠时间增加证明了其中枢抑制活性,并且还可以观察到明显的眼睑下垂。我们的化合物对电休克没有任何活性,CPZ和CPD也是如此。至于抗精神病概况,我们的化合物在群居小鼠中显示出因苯丙胺导致的致死率大幅降低以及很强的抗阿扑吗啡活性。它们还显示出抗攻击作用以及对回避行为的抑制活性,比CPZ强得多。我们还发现了锥体外系效应,如僵住症,这在我们所使用的这类标准镇静剂中很常见。至于植物神经系统现象,这些化合物显示出与剂量相关的降压作用,范围从中度到强烈,可能是由于α受体抑制。对致死剂量肾上腺素的抗肾上腺素活性、抗血清素和抗组胺作用以及其他作用(体温过低、镇痛等)证实,RMI 61 140、RMI 61 144和RMI 61 280具有与CPZ相似且更有效的药理特性。对脑儿茶酚胺代谢的研究表明,它们与CPZ相似,尽管对多巴胺水平的影响较小。

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