Laboratory of Behavioral Neuroscience, Department of Psychology, School of Social Science, University of Crete, Rethymno, Crete, Greece.
Addict Biol. 2013 Mar;18(2):286-96. doi: 10.1111/j.1369-1600.2012.00483.x. Epub 2012 Aug 2.
Cannabidiol is a non-psychotomimetic constituent of Cannabis sativa, which induces central effects in rodents. It has been shown that cannabidiol attenuates cue-induced reinstatement of heroin seeking. However, to the best of our knowledge, its effects on brain stimulation reward and the reward-facilitating effects of drugs of abuse have not yet been examined. Therefore, we investigated the effects of cannabidiol on brain reward function and on the reward-facilitating effect of morphine and cocaine using the intracranial self-stimulation (ICSS) paradigm. Rats were prepared with a stimulating electrode into the medial forebrain bundle (MFB), and a guide cannula into the dorsal raphe (microinjection experiments), and were trained to respond for electrical brain stimulation. A low dose of cannabidiol did not affect the reinforcing efficacy of brain stimulation, whereas higher doses significantly elevated the threshold frequency required for MFB ICSS. Both cocaine and morphine lowered ICSS thresholds. Cannabidiol inhibited the reward-facilitating effect of morphine, but not cocaine. This effect was reversed by pre-treatment with an intra-dorsal raphe injection of the selective 5-HT1A receptor antagonist WAY-100635. The present findings indicate that cannabidiol does not exhibit reinforcing properties in the ICSS paradigm at any of the doses tested, while it decreases the reward-facilitating effects of morphine. These effects were mediated by activation of 5-HT1A receptors in the dorsal raphe. Our results suggest that cannabidiol interferes with brain reward mechanisms responsible for the expression of the acute reinforcing properties of opioids, thus indicating that cannabidiol may be clinically useful in attenuating the rewarding effects of opioids.
大麻二酚是大麻的一种非致幻成分,它会在啮齿类动物中引起中枢效应。已经表明,大麻二酚可以减弱线索诱导的海洛因寻求的复燃。然而,据我们所知,它对大脑刺激奖励和滥用药物的奖励促进作用的影响尚未被研究过。因此,我们使用颅内自我刺激(ICSS)范式研究了大麻二酚对大脑奖励功能的影响,以及对吗啡和可卡因的奖励促进作用的影响。将刺激电极插入内侧前脑束(MFB)中,并将引导套管插入中缝背核(微注射实验),然后对大鼠进行电刺激反应训练。低剂量的大麻二酚不会影响大脑刺激的强化效果,而较高剂量则显著提高了 MFB ICSS 的阈值频率。可卡因和吗啡都降低了 ICSS 的阈值。大麻二酚抑制了吗啡的奖励促进作用,但不抑制可卡因的奖励促进作用。这种作用可被预先注射中缝背核的 5-HT1A 受体拮抗剂 WAY-100635 逆转。本研究结果表明,大麻二酚在任何测试剂量下在 ICSS 范式中均不表现出强化特性,而它降低了吗啡的奖励促进作用。这些作用是通过中缝背核 5-HT1A 受体的激活介导的。我们的结果表明,大麻二酚干扰了大脑奖励机制,负责表达阿片类药物的急性强化特性,因此表明大麻二酚可能在减轻阿片类药物的奖励作用方面具有临床应用价值。