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与尼古丁相关的化合物对小鼠的一些中枢效应。

Some central effects in mice of compounds related to nicotine.

作者信息

Barlow R B, Oliverio A, Satta M, Thompson G M

出版信息

Br J Pharmacol. 1970 Jul;39(3):647-52. doi: 10.1111/j.1476-5381.1970.tb10372.x.

Abstract
  1. Some hydroxy-, amino-, and methoxy- phenylalkyltrimethylammonium compounds, beta-pyridylmethyl- dimethylamine and pyrrolidine, and beta-pyridylethyltrimethylammonium, were tested on avoidance learning in mice and their effects were compared with those of (-)-nicotine.2. The o- and m- hydroxybenzyl-, o-hydroxyphenethyl- and m-hydroxyphenylpropyl- trimethylammonium compounds improved performance; (-)-nicotine, in one-quarter of the dose, had similar effects. The m- and p-hydroxyphenethyl-, o-hydroxyphenylpropyl- and o- and p- aminobenzyl, and o-, m-, and p- aminophenethyl-trimethylammonium compounds impaired performance.3. (-)-Nicotine and m-hydroxyphenylpropyltrimethylammonium appeared also to enhance memory consolidating processes.4. The central actions of some of the compounds suggest that the possibility that they can penetrate into the central nervous system should not be ruled out even though they are quaternary salts.5. No correlation was found between the effects of the compounds on avoidance learning and on the frog rectus muscle. Though the differences may be due to differences in access to the central nervous system, it is also possible that the receptors associated with learning processes are different from those in the frog rectus and possibly more specialized.
摘要
  1. 对一些羟基、氨基和甲氧基苯基烷基三甲基铵化合物、β-吡啶基甲基二甲胺和吡咯烷以及β-吡啶基乙基三甲基铵进行了小鼠回避学习实验,并将其效果与(-)-尼古丁的效果进行了比较。

  2. 邻羟基苄基、间羟基苄基、邻羟基苯乙基和间羟基苯丙基三甲基铵化合物提高了实验表现;(-)-尼古丁在四分之一剂量时具有类似效果。间羟基苯乙基、对羟基苯乙基、邻羟基苯丙基、邻氨基苄基、间氨基苄基、对氨基苄基以及邻氨基苯乙基、间氨基苯乙基、对氨基苯乙基三甲基铵化合物则损害了实验表现。

  3. (-)-尼古丁和间羟基苯丙基三甲基铵似乎也能增强记忆巩固过程。

  4. 某些化合物的中枢作用表明,即使它们是季铵盐,也不能排除其穿透进入中枢神经系统的可能性。

  5. 未发现这些化合物对回避学习的影响与对青蛙直肌的影响之间存在相关性。虽然差异可能是由于进入中枢神经系统的途径不同,但也有可能与学习过程相关的受体与青蛙直肌中的受体不同,并且可能更具特异性。

相似文献

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Effects of oxiracetam-nicotine combinations on active and passive avoidance learning in mice.
Pharmacol Biochem Behav. 1991 May;39(1):197-200. doi: 10.1016/0091-3057(91)90421-w.

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