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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Cocaine dose and self-administration history, but not initial cocaine locomotor responsiveness, affects sensitization to the motivational effects of cocaine in rats
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Cocaine dose and self-administration history, but not initial cocaine locomotor responsiveness, affects sensitization to the motivational effects of cocaine in rats

机译:可卡因的剂量和自我给药史,但不影响初始可卡因的运动反应,会影响对可卡因对大鼠动力作用的敏感性

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Cocaine addiction is a significant and complex disease. Part of this complexity is caused by the variability of the drug experience early in drug use (initial responsiveness, amount of use, etc.). In rats, individual differences in initial cocaine responsiveness and cocaine self-administration history both predict the development of cocaine sensitization, a putative mechanism contributing to the development of cocaine addiction. Here, we sought to determine the role of these factors and cocaine dose on the development of sensitization to cocaine's motivational effects during the earliest stages of self-administration. Rats were classified as either low or high cocaine responders (LCRs or HCRs, respectively) based on acute cocaine-induced locomotor activity (10 mg/kg i.p.) before learning to self-administer cocaine (0.6 mg/kg/infusion i.v.) under a fixed ratio 1 (FR1) schedule of reinforcement. After acquisition, rats self-administered cocaine (0.6 or 1.2 mg/kg/infusion) under a progressive ratio (PR) schedule of reinforcement either immediately or after an additional five FR1 sessions (0.6 or 1.2 mg/kg/infusion). No LCR/HCR differences in sensitization were observed. However, regardless of LCR/HCR classification, exposure to the higher dose of cocaine produced sensitization to cocaine's motivational effects on the PR schedule (i.e., increased break points) and an escalation of consumption on the FR schedule. Thus, our results reveal a novel model for studying escalation and sensitization very early after acquisition and suggest that sensitization may be important in the earliest stages of the cocaine addiction process.
机译:可卡因成瘾是一种重大而复杂的疾病。这种复杂性的部分原因是药物使用早期的药物体验变化(初始反应性,使用量等)引起的。在大鼠中,初始可卡因反应能力和可卡因自我给药史的个体差异均预示了可卡因致敏的发展,这是导致可卡因成瘾发展的一种推测机制。在这里,我们试图确定这些因素和可卡因剂量在自我管理的最早阶段对可卡因的动机作用致敏性发展中的作用。根据急性可卡因诱导的自发活动(10 mg / kg ip),将大鼠分为可卡因反应低或高(分别为LCRs或HCR),然后在以下条件下学会自我给药可卡因(0.6 mg / kg /滴注)。固定比例1(FR1)的加固时间表。采集后,大鼠立即或在另外五次FR1疗程(0.6或1.2 mg / kg /滴注)后按递增比例(PR)强化方案自行施用可卡因(0.6或1.2 mg / kg /滴注)。在敏化方面未观察到LCR / HCR差异。但是,无论LCR / HCR的分类如何,暴露于较高剂量的可卡因都会对可卡因对PR时间表的激励作用(即增加的断点)产生敏感性,并在FR时间表上增加消费量。因此,我们的结果揭示了一种新的模型,用于在获取后很早就研究升级和致敏性,并表明致敏性在可卡因成瘾过程的最早阶段可能很重要。

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