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咖啡因的致焦虑作用:大鼠实验研究

Anxiogenic action of caffeine: an experimental study in rats.

作者信息

Bhattacharya S K, Satyan K S, Chakrabarti A

机构信息

Department of Pharmacology, Banaras Hindu University, Varanasi, India.

出版信息

J Psychopharmacol. 1997;11(3):219-24. doi: 10.1177/026988119701100304.

Abstract

The anxiogenic action of caffeine (10, 25 and 50 mg/kg, i.p.) was investigated in rats and compared with that of yohimbine (2 mg/kg, i.p.). The experimental methods used were the open-field, elevated plus-maze, social interaction and novelty-suppressed feeding latency tests. Caffeine produced a dose-related profile of behavioural changes, which were qualitatively similar to those induced by yohimbine and which indicate an anxiogenic activity in rodents. Thus, both the drugs reduced ambulation and rears, and increased immobility and defaecation in the open-field test. They decreased the number of entries and time spent on the open arms of the elevated-plus maze, reduced social interaction in paired rats and increased the feeding latency in an unfamiliar environment in 48-h food-deprived rats. Lorazepam, a well known benzodiazepine anxiolytic agent, attenuated the anxiogenic effects of caffeine and yohimbine. Subchronic administration of caffeine (50 mg/kg, i.p.) for 21 days, in different groups of animals, induced a significant degree of tolerance in the elevated plus-maze test, which was statistically significant after 14 and 21 days' treatment. Yohimbine, however, did not induce similar tolerance. When caffeine (50 mg/kg, i.p.) was withdrawn after 21 days' administration, to a separate group of rats, significant withdrawal anxiety was observed 48 h later as noted in the elevated plus-maze test. The investigations support clinical evidence of caffeine-induced anxiety, tolerance to anxiety on continued use, and withdrawal anxiety in chronic caffeine-containing beverage users.

摘要

研究了咖啡因(腹腔注射,剂量为10、25和50mg/kg)对大鼠的致焦虑作用,并与育亨宾(腹腔注射,剂量为2mg/kg)进行了比较。所采用的实验方法包括旷场试验、高架十字迷宫试验、社交互动试验和新奇抑制摄食潜伏期试验。咖啡因产生了与剂量相关的行为变化,这些变化在性质上与育亨宾诱导的变化相似,表明在啮齿动物中具有致焦虑活性。因此,在旷场试验中,两种药物均减少了大鼠的走动和站立次数,增加了不动时间和排便次数。它们减少了进入高架十字迷宫开放臂的次数和在开放臂上停留的时间,减少了成对大鼠之间的社交互动,并增加了48小时未进食的大鼠在陌生环境中的摄食潜伏期。众所周知的苯二氮䓬类抗焦虑药劳拉西泮减弱了咖啡因和育亨宾的致焦虑作用。在不同组动物中,亚慢性给予咖啡因(腹腔注射,50mg/kg)21天,在高架十字迷宫试验中诱导了显著程度的耐受性,在治疗14天和21天后具有统计学意义。然而,育亨宾并未诱导出类似的耐受性。在21天给药后,将咖啡因(腹腔注射,50mg/kg)撤去,给予另一组大鼠,48小时后观察到明显的戒断焦虑,如在高架十字迷宫试验中所示。这些研究支持了咖啡因诱导焦虑、持续使用后对焦虑产生耐受性以及慢性饮用含咖啡因饮料者出现戒断焦虑的临床证据。

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