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A Single Exposure to Amphetamine Is Sufficient to Induce Long-Term Behavioral Neuroendocrine and Neurochemical Sensitization in Rats

机译:苯丙胺的单次暴露足以诱导大鼠的长期行为神经内分泌和神经化学增敏作用

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Repeated treatment with psychostimulant drugs causes long-lasting behavioral sensitization and associated neuroadaptations. Although sensitization induced by a single psychostimulant exposure has also been reported, information on the behavioral and neurochemical consequences of a single psychostimulant exposure is sparse. Therefore, to evaluate whether behavioral sensitization evoked by single and repeated psychostimulant pretreatment regimens represent the same neurobiological phenomenon, the time-dependent expression of behavioral, neurochemical, and neuroendocrine sensitization after a single exposure to amphetamine was investigated in rats. A single exposure to amphetamine (5 mg/kg, i.p.) caused context-independent sensitization of the locomotor effects of amphetamine, which intensified over time. Thus, sensitization to amphetamine was marginal at 3 d after treatment and more evident after 1 week, whereas 3 weeks after treatment, profound sensitization, as well as cross-sensitization, to cocaine was observed. Amphetamine pretreatment caused an increase in the electrically evoked release of [3H]dopamine from nucleus accumbens, caudate putamen, and medial prefrontal cortex slices and of [14C]acetylcholine from accumbens and caudate slices. The hyperreactivity of dopaminergic nerve terminals appeared to parallel the development of locomotor sensitization, i.e., whereas hyperreactivity of accumbens dopaminergic terminals increased between 3 d and 3 weeks after treatment, the hyperreactivity of medial prefrontal dopaminergic terminals decreased. Pre-exposure to amphetamine also sensitized the hypothalamus–pituitary–adrenal axis response to amphetamine at 1 and 3 weeks, but not at 3 d after treatment. Because these data closely resemble those reported previously for repeated amphetamine pretreatment, it is concluded that a single exposure to amphetamine is sufficient to induce long-term behavioral, neurochemical, and neuroendocrine sensitization in rats.
机译:反复使用精神刺激药物治疗会导致长期的行为敏化和相关的神经适应。尽管也曾报道过一次单一的精神兴奋剂暴露引起的致敏作用,但是关于一次单一的精神兴奋剂暴露的行为和神经化学后果的信息很少。因此,为了评估单一和重复的精神刺激剂预处理方案引起的行为敏化是否代表相同的神经生物学现象,研究了大鼠一次接触苯丙胺后行为,神经化学和神经内分泌敏化的时间依赖性表达。一次接触苯丙胺(5 mg / kg,腹膜内)会引起与环境无关的苯丙胺运动效应的敏化作用,随着时间的推移会加剧。因此,对苯丙胺的致敏作用在治疗后3 d很小,而在1周后更为明显,而在治疗3周后,观察到对可卡因的深刻致敏作用以及交叉致敏作用。苯丙胺预处理引起伏伏核,尾状壳核和内侧前额叶皮层切片中的[ 3 H]多巴胺的电诱发释放增加,以及[ 14 C]乙酰胆碱的电诱发释放增加伏状和尾状切片。多巴胺能神经末梢的高反应性似乎与运动性敏化的发展平行,即,伏隔多巴胺能末梢的高反应性在治疗后3 d至3周之间升高,内侧前额叶多巴胺能末梢的高反应性下降。苯丙胺暴露前也可在治疗后1周和3周而不是3天后使下丘脑-垂体-肾上腺轴对苯丙胺敏感。由于这些数据与先前报道的重复安非他明预处理的数据非常相似,因此得出的结论是,单次接触安非他明足以引起大鼠的长期行为,神经化学和神经内分泌致敏。

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