首页> 外文期刊>Neurochemical research >Intra-accumbal Cannabinoid Agonist Attenuated Reinstatement but not Extinction Period of Morphine-Induced Conditioned Place Preference; Evidence for Different Characteristics of Extinction Period and Reinstatement
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Intra-accumbal Cannabinoid Agonist Attenuated Reinstatement but not Extinction Period of Morphine-Induced Conditioned Place Preference; Evidence for Different Characteristics of Extinction Period and Reinstatement

机译:宫内大麻加毒剂激动剂减毒恢复但不会消灭吗啡诱导的条件偏好; 灭绝时期不同特点的证据和恢复

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Abstract The brain reward system consists of the ventral tegmental area that sends its dopaminergic projections to the forebrain, cortical areas, amygdala and largely to the nucleus accumbens (NAc). The present study aims were to investigate the effects of bilateral intra-accumbal microinjection of WIN55,212-2, a CB1 receptor agonist, on the duration of extinction period and reinstatement to morphine by the conditioned place preference (CPP) paradigm in the rat. Forty-six adult male albino Wistar rats received intra-accumbal WIN55,212-2 [p0.5, 1 and 2?mM/0.5?μl dimethyl sulfoxide (DMSO)] injections bilaterally. To induce CPP, morphine (5?mg/kg) was injected subcutaneously over three consecutive days. The results showed that intra-NAc administration of WIN55,212-2 during the extinction period had no effect on its duration but single administration of the1?mM/0.5?μl DMSO dose just before the reinstatement phase significantly attenuated its conditioning score. This is the first time that interactions of opioid and cannabinoid systems by local activation of CB1 receptors in the NAc during extinction and morphine-induced reinstatement were investigated. The CB1 agonist can inhibit and eliminate the reward-associated memory of morphine and the conditioning score in reinstatement but not in the extinction period. Our findings suggest that the extinction period and reinstatement could occur through different mechanisms.
机译:摘要脑奖励系统由腹侧三脑,将其多巴胺能突出突出到前脑,皮质区域,杏仁菌,并且主要用于核心腺(NAC)。本研究旨在探讨双侧腹腔内微注射Win55,212-2的影响,CB1受体激动剂在消灭时期的持续时间和通过大鼠的条件偏好(CPP)范例恢复对吗啡的持续时间。四十六个成年白醇Wistar大鼠接受了两侧宫颈内的宫内Win55,212-2 [P0.5,1和2?mm / 0.5×0.5·μl二甲基磺氧化物(DMSO)]。为了诱导CPP,将吗啡(5?Mg / kg)皮下注射在连续三天内注射。结果表明,在消灭期间,NAC内部施用Win55,212-2在其持续时间内没有影响,但在恢复相比之前,单次施用1μlαmm/ 0.5?μldmso剂量。研究是首次通过在消灭和吗啡诱导的恢复过程中通过局部激活NAC局部激活CB1受体的阿片类药物和大麻素系统的相互作用。 CB1激动剂可以抑制并消除吗啡的奖励相关记忆,并在恢复时进行调理得分,但不在消除期间。我们的研究结果表明,消化期和恢复可能通过不同的机制发生。

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