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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Intravenous cocaine precipitates panic-like flight responses and lasting hyperdefensiveness in laboratory rats.
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Intravenous cocaine precipitates panic-like flight responses and lasting hyperdefensiveness in laboratory rats.

机译:静脉注射可卡因可在实验室大鼠中引起惊恐样的飞行反应和持久的超防御作用。

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There is an emerging body of clinical evidence that cocaine use in humans can result in serious fear or panic-related emotional disturbances. The present study evaluated the effects of intravenous cocaine administration upon defensive responses of rats to a threatening conspecific in a test situation, an oval runaway, permitting the display of the full range of the rat defensive repertoire. A battery of tests was employed to evaluate avoidance/escape, flight, freezing, defensive upright and defensive attack behaviors. In the first experiment male Long-Evans rats implanted with a chronic indwelling jugular catheter were placed in the runway and tested immediately after administration of either 0, 1, or 4 mg/kg of cocaine hydrochloride. The 4-mg/kg dose produced a dramatic flight response, the direction of which depended upon the direction of the approaching threat source. The same dose produced increased defensive upright postures during forced contact with the stimulus animal. Experiment 2 examined the time course for cocaine-induced hyperdefensiveness. Rats were administered either saline or 4 mg/kg cocaine intravenously and were tested following a delay of either 0, 5, 15, or 30 min following infusion. Cocaine-treated rats again displayed high levels of flight, which declined with increased time between infusion and testing. However, increased defensiveness persisted even at the 30 min delay for several defensive measures including avoidance, freezing, and defensive upright posture. Thus, following an initial period of rapid flight with intravenous cocaine administration, there was a lasting hyperdefensiveness in cocaine-treated rats. The present results suggest that cocaine may exert its panic-producing effects by acting upon neurobehavioral systems subserving defensive behavior, and that understanding of these systems is critical for understanding the neurobiology of panic disorder.
机译:有大量的临床证据表明,在人类中使用可卡因会导致严重的恐惧或与恐慌相关的情绪障碍。本研究评估了在试验情况下椭圆形失控的情况下,静脉注射可卡因对大鼠对威胁性种的防御反应的影响,从而可以显示整个大鼠防御性谱系。使用一系列测试来评估避让/逃生,逃跑,冻结,防御性直立和防御性攻击行为。在第一个实验中,将植入了慢性留置颈静脉导管的雄性Long-Evans大鼠放在跑道上,并在施用0、1或4 mg / kg的可卡因盐酸盐后立即进行测试。 4 mg / kg剂量产生了戏剧性的飞行响应,其方向取决于接近威胁源的方向。在与刺激动物强迫接触期间,相同剂量会产生增加的防御性直立姿势。实验2检验了可卡因诱发的高防御反应的时程。给大鼠静脉内注射盐水或4 mg / kg可卡因,并在输注后延迟0、5、15或30分钟进行测试。用可卡因治疗的大鼠再次表现出高水平的飞行,随输注和测试之间时间的增加而下降。但是,即使在延迟30分钟后采取一些防御措施(包括避免,冻结和防御直立姿势),防御能力仍然持续存在。因此,在通过静脉注射可卡因开始快速飞行的最初阶段之后,可卡因治疗的大鼠出现了持久的防御过度。目前的结果表明,可卡因可能通过作用于保护防御行为的神经行为系统而发挥其惊恐产生作用,而对这些系统的理解对于理解惊恐症的神经生物学至关重要。

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