Pharmacological properties of AF 1161, a new psychotropic drug

B. Silvestrini, V. Cioli, S. Burberi, B. Catanese
{"title":"Pharmacological properties of AF 1161, a new psychotropic drug","authors":"B. Silvestrini,&nbsp;V. Cioli,&nbsp;S. Burberi,&nbsp;B. Catanese","doi":"10.1016/0028-3908(68)90069-5","DOIUrl":null,"url":null,"abstract":"<div><p>A series of pharmacological trials conducted on AF 1161 are described. AF 1161 explicates, at doses much lower than toxic ones, certain effects on behaviour characterized by a picture of sedation and diminished reactivity to external stimuli. Even at very high doses, the drug does not provoke catatonia, paralysis, or a true hypnotic state. Death is preceded by a state of prostration, overtaken by clonic convulsion. The conditioned avoidance reflex in rats and reactions to different types of painful stimuli are inhibited at doses that scarcely influence general behaviour. Duration of sleep induced by hexobarbital is increased immediately after AF 1161 administration, but returns to normal after 24 hr. No significant hypothermic effect in normal animals was noted. Toxicity of amphetamine in grouped mice is inhibited. A depressant action on the linguomandibular reflex and, no a slight extent, on the knee jerk has been observed. AF 1161 possesses a very slight anti-histamine action, a moderate adrenolytic action and a powerful anti-serotonin action. Convulsions due to pentetrazol, electroshock and strychnine are not inhibited. A local anesthetic effect was also observed.</p><p>These results are discussed, and possible therapeutic use in man of AF 1161 is postulated.</p></div>","PeriodicalId":14111,"journal":{"name":"International journal of neuropharmacology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1968-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0028-3908(68)90069-5","citationCount":"64","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of neuropharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0028390868900695","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 64

Abstract

A series of pharmacological trials conducted on AF 1161 are described. AF 1161 explicates, at doses much lower than toxic ones, certain effects on behaviour characterized by a picture of sedation and diminished reactivity to external stimuli. Even at very high doses, the drug does not provoke catatonia, paralysis, or a true hypnotic state. Death is preceded by a state of prostration, overtaken by clonic convulsion. The conditioned avoidance reflex in rats and reactions to different types of painful stimuli are inhibited at doses that scarcely influence general behaviour. Duration of sleep induced by hexobarbital is increased immediately after AF 1161 administration, but returns to normal after 24 hr. No significant hypothermic effect in normal animals was noted. Toxicity of amphetamine in grouped mice is inhibited. A depressant action on the linguomandibular reflex and, no a slight extent, on the knee jerk has been observed. AF 1161 possesses a very slight anti-histamine action, a moderate adrenolytic action and a powerful anti-serotonin action. Convulsions due to pentetrazol, electroshock and strychnine are not inhibited. A local anesthetic effect was also observed.

These results are discussed, and possible therapeutic use in man of AF 1161 is postulated.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
新型精神药物af1161的药理性质
描述了对af1161进行的一系列药理试验。af1161表明,在剂量远低于毒性剂量的情况下,对以镇静和对外部刺激反应减弱为特征的行为产生某些影响。即使在非常高的剂量下,该药也不会引起紧张症、麻痹或真正的催眠状态。死亡之前是一种萎靡不振的状态,随后是阵挛性抽搐。大鼠的条件回避反射和对不同类型的痛苦刺激的反应在几乎不影响一般行为的剂量下被抑制。六巴比妥诱导的睡眠时间在给药后立即增加,但在24小时后恢复正常。在正常动物中未发现明显的低温效应。安非他明对分组小鼠的毒性受到抑制。对下颌反射有抑制作用,对膝跳也有一定程度的抑制作用。AF 1161具有非常轻微的抗组胺作用,中度的肾上腺素溶解作用和强大的抗血清素作用。戊四唑、电击和士的宁引起的惊厥不受抑制。局部麻醉作用也被观察到。对这些结果进行了讨论,并对AF 1161在男性中的可能治疗用途进行了假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Experimental alteration of tryptophan metabolism by methionine: Neuropharmacologic implications Noradrenaline sensitive cells in cat cerebral cortex Alteration of centrally mediated cardiovascular manifestations by intraventricular pronethalol and phentolamine Evidence for biogenic amine receptors in toad sciatic nerves Comparative study of the actions of nicotine and succinylcholine on the monosynaptic reflex and spindle afferent activity
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1