Maj Institute of Pharmacology, Polish Academy of Sciences, Department of Drug Addiction Pharmacology, Kraków, Poland.
Maj Institute of Pharmacology, Polish Academy of Sciences, Department of Drug Addiction Pharmacology, Kraków, Poland.
Pharmacol Rep. 2019 Oct;71(5):870-878. doi: 10.1016/j.pharep.2019.05.001. Epub 2019 May 7.
Several studies strongly support the role of the dopamine D-like and glutamate mGlu receptors in psychostimulant reward and relapse.
The present study employed cocaine or MDMA self-administration with yoked-triad procedure in rats to explore whether extinction training affects the drug-seeking behavior and the D-like and mGlu receptor B and K values in several regions of the animal brain.
Both cocaine and MDMA rats developed maintenance of self-administration, but MDMA evoked lower response rates and speed of self-administration acquisition. During reinstatement tests, cocaine or MDMA seeking behavior was produced by either exposure to the drug-associated cues or drug-priming injections. The extinction training after cocaine self-administration did not alter significantly D-like receptor expression the in the limbic and subcortical brain areas, while MDMA yoked rats showed a decrease of the Dlike binding density in the nucleus accumbens and increase in the hippocampus and a rise of affinity in the striatum and hippocampus. Interestingly, in the prefrontal cortex a reduction in the mGlu receptor density in cocaine- or MDMA-abstinent rats was demonstrated, with significant effects being observed after previous MDMA exposure. Moreover, rats self-administered cocaine showed a rise in the density of mGlu receptor for the nucleus accumbens.
This study first time shows that abstinence followed extinction training after cocaine or MDMA self- or passive-injections changes the D-like and mGlu density and affinity. The observed changes in the expression of both receptors are brain-region specific and related to either pharmacological and/or motivational features of cocaine or MDMA.
多项研究有力地支持多巴胺 D 样和谷氨酸 mGlu 受体在精神兴奋剂奖励和复吸中的作用。
本研究采用可卡因或 MDMA 自我给药与偶联三联体程序在大鼠中进行,以探讨消退训练是否会影响觅药行为以及动物大脑中几个区域的 D 样和 mGlu 受体 B 和 K 值。
可卡因和 MDMA 大鼠均维持自我给药,但 MDMA 诱发的反应率和自我给药获得速度较低。在复吸测试中,可卡因或 MDMA 的觅药行为是通过暴露于药物相关线索或药物引发注射引起的。可卡因自我给药后的消退训练并没有显著改变边缘和皮质下脑区的 D 样受体表达,而 MDMA 偶联大鼠显示出伏隔核 D 样结合密度降低,海马体增加,纹状体和海马体亲和力增加。有趣的是,在前额皮质中,可卡因或 MDMA 戒断大鼠的 mGlu 受体密度降低,而先前暴露于 MDMA 后则出现显著影响。此外,自我给予可卡因的大鼠显示出伏隔核 mGlu 受体密度增加。
这项研究首次表明,可卡因或 MDMA 自我给药或被动注射后,戒断后消退训练会改变 D 样和 mGlu 受体的密度和亲和力。两种受体表达的观察到的变化具有脑区特异性,与可卡因或 MDMA 的药理学和/或动机特征有关。