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取代苯丙胺衍生物。II. 与单胺能神经元相关的小鼠行为效应。

Substituted amphetamine derivatives. II. Behavioural effects in mice related to monoaminergic neurones.

作者信息

Ogren S O, Ross S B

出版信息

Acta Pharmacol Toxicol (Copenh). 1977 Oct;41(4):353-68. doi: 10.1111/j.1600-0773.1977.tb02674.x.

Abstract

The effects of the amphetamine derivatives (+/-)-amphetamine (A), 2-, 3- and 4-chloroamphetamine (CA), 4-methylamphetamine (MA) and chlorphentermine (CP) in producing central stimulation (increase in motor activity), antagonism of the reserpine syndrome, potentiation of 1-dopa and 5-hydroxytryptophan (5HTP) responses in mice were investigated. The inhibitors of the membrane amine uptake despramine (DMI) and chlorimipramine (CI) were also included in the study. It was found that the order in central stimulating potency was A greater than 3-CA = 4-CA greater than MA greater than CP. 2-CA, DMI and CI decreased the motor activity. All the compounds potentiated the 1-dopa response with the order of activity: 4-MA greater than A greater than 2-CA = 3-CA = 4-CA = CI greater than or equal to DMI greater than CP. The decrease in motor activity (sedation) produced by reserpine was only reversed by A greater than or equal to 3-CA greater than 2-CA. alpha-Methyltyrosine but not parachlorophenylalanine, antagonized the reversal effect. Three of the compounds (3-CA, 4-CA and MA) produced head-twitches in the reserpinized mice. The 5-HTP syndrome was potentiated in order of potency by MA = 4-CA greater than CI greater than CP greater than 3-CA whereas A, 2-CA and DMI had no effect.

摘要

研究了苯丙胺衍生物(±)-苯丙胺(A)、2-、3-和4-氯苯丙胺(CA)、4-甲基苯丙胺(MA)和氯苯丁胺(CP)在小鼠中产生中枢兴奋(运动活动增加)、拮抗利血平综合征、增强左旋多巴和5-羟色氨酸(5HTP)反应的作用。膜胺摄取抑制剂去甲丙咪嗪(DMI)和氯米帕明(CI)也纳入了该研究。结果发现,中枢兴奋效力顺序为A大于3-CA = 4-CA大于MA大于CP。2-CA、DMI和CI降低了运动活动。所有化合物均增强了左旋多巴反应,活性顺序为:4-MA大于A大于2-CA = 3-CA = 4-CA = CI大于或等于DMI大于CP。利血平引起的运动活动降低(镇静)仅被A大于或等于3-CA大于2-CA所逆转。α-甲基酪氨酸而非对氯苯丙氨酸拮抗了这种逆转作用。其中三种化合物(3-CA、4-CA和MA)在利血平化小鼠中引起了头部抽搐。MA = 4-CA大于CI大于CP大于3-CA按效力顺序增强了5-HTP综合征,而A、2-CA和DMI则无作用。

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