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一项关于去甲肾上腺素在拟精神病药物所致大鼠行为变化中作用的研究。

A study of the role of noradrenaline in behavioral changes produced in the rat by psychotomimetic drugs.

作者信息

Sugrue M F

出版信息

Br J Pharmacol. 1969 Feb;35(2):243-52. doi: 10.1111/j.1476-5381.1969.tb07983.x.

Abstract
  1. LSD-25, psilocybin and JB-329 reduced the noradrenaline content of the rat hypothalamus.2. All three drugs affected the acquisition of a conditioned avoidance response, LSD-25 and psilocybin retarding and JB-329 enhancing the acquisition. With the exception of JB-329, doses affecting the acquisition of a conditioned avoidance response were lower than those required to decide hypothalamic noradrenaline concentrations. The time of peak drug effect on the acquisition of a conditioned avoidance response occurred approximately 1.5 hr after injection as opposed to 3 hr in the case of noradrenaline content.3. The amount of LSD-25, psilocybin and JB-329 necessary to elicit gross behavioural excitation was similar to the dose producing noradrenaline depletion. Here also the peak behavioural effect was detected earlier.4. Pretreatment with reserpine and alpha-MT had no effect on the intensity of gross behavioural excitation induced by LSD-25 and psilocybin but shortened the duration of the response. The excitation induced by JB-329 was abolished by reserpine pretreatment and was markedly reduced both in intensity and duration by the prior injection of alpha-MT.
摘要
  1. LSD - 25、裸盖菇素和JB - 329降低了大鼠下丘脑的去甲肾上腺素含量。

  2. 这三种药物均影响条件性回避反应的习得,LSD - 25和裸盖菇素延缓其习得,而JB - 329则增强其习得。除JB - 329外,影响条件性回避反应习得的剂量低于改变下丘脑去甲肾上腺素浓度所需的剂量。药物对条件性回避反应习得产生最大效应的时间约在注射后1.5小时,而去甲肾上腺素含量方面则为3小时。

  3. 引发明显行为兴奋所需的LSD - 25、裸盖菇素和JB - 329的量与导致去甲肾上腺素耗竭的剂量相似。此处行为效应的峰值也更早出现。

  4. 用利血平和α - MT预处理对LSD - 25和裸盖菇素诱导的明显行为兴奋强度没有影响,但缩短了反应持续时间。利血平预处理可消除JB - 329诱导的兴奋,而预先注射α - MT则使其强度和持续时间均显著降低。

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本文引用的文献

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STUDIES ON BIOGENIC AMINES AND PSYCHOACTIVE DRUG ACTIONS, WITH SPECIAL REFERENCE TO LYSERGIC ACID DIETHYL AMIDE.
Trans N Y Acad Sci. 1964 Jan;26:369-76. doi: 10.1111/j.2164-0947.1964.tb01258.x.
4
Psychotomimetic drugs and brain biogenic amines.
Am J Psychiatry. 1963 Mar;119:843-50. doi: 10.1176/ajp.119.9.843.
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