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慢性给予阿米替林可抑制大鼠对喹哌嗪的头部抽搐反应,而氟伏沙明或西酞普兰则无此作用。

Inhibition of head twitch response to quipazine in rats by chronic amitriptyline but not fluvoxamine or citalopram.

作者信息

Pawłowski L, Melzacka M

出版信息

Psychopharmacology (Berl). 1986;88(3):279-84. doi: 10.1007/BF00180825.

Abstract

Chronic (twice daily/14 days), but not acute, treatment with 10 mg/kg PO amitriptyline reduced the number of quipazine (5 mg/kg)-induced head twitches in rats, measured 2 h (but not 72 h) after the last administration of the drug. Similar treatment with fluvoxamine or citalopram, which are more potent and much more specific serotonin uptake inhibitors than amitriptyline, did not affect the quipazine-induced response. In acute experiments, fluvoxamine (10 mg/kg PO) and citalopram (10 mg/kg PO) potentiated the head twitch reaction induced by L-5-hydroxytryptophan (50 mg/kg IP) given together with Ro 4-4602 (25 mg/kg IP), a peripheral decarboxylase inhibitor. Amitriptyline (10 mg/kg PO) slightly decreased the number of L-5-hydroxytryptophan (5-HTP)-induced head twitches. Higher doses of amitriptyline (20-40 mg/kg PO) also inhibited the quipazine-induced head twitch reaction. The brain level of amitriptyline measured 0.5-24 h after the last oral administration of the chronic dose of 10 mg/kg was always much higher than that observed at the same time intervals after an acute oral dose of 20 or 40 mg/kg. The results obtained indicate that a postsynaptic rather then presynaptic mechanism is responsible for the development of subsensitivity of the central serotonin receptors in the course of chronic treatment with amitriptyline.

摘要

连续14天每天两次口服10mg/kg阿米替林进行慢性治疗(而非急性治疗)可减少大鼠中由5mg/kg喹哌嗪诱导的头部抽搐次数,在最后一次给药后2小时(而非72小时)测量。用氟伏沙明或西酞普兰进行类似治疗,它们比阿米替林更有效且更具特异性的5-羟色胺摄取抑制剂,并未影响喹哌嗪诱导的反应。在急性实验中,氟伏沙明(10mg/kg口服)和西酞普兰(10mg/kg口服)增强了由L-5-羟色氨酸(50mg/kg腹腔注射)与外周脱羧酶抑制剂Ro 4-4602(25mg/kg腹腔注射)一起给药诱导的头部抽搐反应。阿米替林(10mg/kg口服)略微减少了L-5-羟色氨酸(5-HTP)诱导的头部抽搐次数。更高剂量的阿米替林(20 - 40mg/kg口服)也抑制了喹哌嗪诱导的头部抽搐反应。在最后一次口服10mg/kg慢性剂量后0.5 - 24小时测量的阿米替林脑内水平始终远高于急性口服20或40mg/kg后相同时间间隔观察到的水平。所得结果表明,在阿米替林慢性治疗过程中,中枢5-羟色胺受体亚敏感性发展的原因是突触后而非突触前机制。

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