Pomierny-Chamiolo Lucyna, Miszkiel Joanna, Frankowska Malgorzata, Bystrowska Beata, Filip Malgorzata
Department of Toxicology, Faculty of Pharmacy, Jagiellonian University, Medical College, Medyczna 9, PL 30-688 Kraków, Poland.
Institute of Pharmacology Polish Academy of Sciences, Laboratory of Drug Addiction Pharmacology, Smętna 12, PL 31-343 Kraków, Poland.
Brain Res. 2017 Jan 15;1655:66-76. doi: 10.1016/j.brainres.2016.11.014. Epub 2016 Nov 18.
Several behavioral findings highlight the importance of glutamatergic transmission and its metabotropic receptor type 5 (mGlu) in the controlling of cocaine reward and seeking behaviors. The molecular or neurochemical nature of such interactions is not well recognized, so in the present paper we determine if cocaine self-administration and extinction/reinstatement models with the yoked triad control procedure alter mGlu receptor density in rats. [³H]MPEP was used to evaluate mGlu receptors density and affinity in selected brain structures, while immunofluorescence analysis was used to detect changes in mGlu receptors' brain location. Cocaine self-administration and yoked cocaine delivery evoked a significant elevation in mGlu receptors' density in the dorsal striatum, while receptor protein expression was importantly elevated in the substantia nigra and reduced in the nucleus accumbens shell. Cocaine administration followed by 10 extinction training sessions resulted in biphasic mGlu receptor density changes in the prefrontal cortex-nucleus accumbens pathway. mGlu receptors' up-regulation was noted for cocaine self-administration and extinction training in the hippocampus and in yoked cocaine controls following drug abstinence in the dorsal striatum. A cocaine priming dose (but not a saline priming) resulted in a significant decrease of mGlu receptors' density in the nucleus accumbens of rats previously treated with the drug and in the hippocampus of rats previously self-administered cocaine. The latter decrease in mGlu receptors' density and protein expression in the hippocampus was parallel to an increase in [³H]MPEP affinity and opposite to a rise observed after single cocaine administration (ip) to drug-naïve yoked saline controls. Additionally, we also observed a significant elevation in the protein expression of the tested receptors in the limbic cortex in both cocaine groups. The present results shown modality dependent and brain-region specific changes in mGlu receptors' localization and membrane specific binding.
多项行为学研究结果凸显了谷氨酸能传递及其代谢型受体5(mGlu)在控制可卡因奖赏和觅药行为中的重要性。此类相互作用的分子或神经化学本质尚未得到充分认识,因此在本文中,我们研究了采用配对三联体对照程序的可卡因自身给药及消退/复吸模型是否会改变大鼠体内mGlu受体的密度。利用[³H]MPEP评估选定脑区结构中mGlu受体的密度和亲和力,同时采用免疫荧光分析检测mGlu受体在脑内位置的变化。可卡因自身给药和配对给予可卡因可使背侧纹状体中mGlu受体的密度显著升高,而黑质中受体蛋白表达显著升高,伏隔核壳中的表达则降低。给予可卡因后进行10次消退训练,导致前额叶皮质-伏隔核通路中mGlu受体密度出现双相变化。在海马体中,可卡因自身给药和消退训练以及背侧纹状体戒断后的配对可卡因对照组中,mGlu受体出现上调。给予可卡因引发剂量(而非生理盐水引发剂量)可使先前接受过药物治疗的大鼠伏隔核以及先前自身给药可卡因的大鼠海马体中mGlu受体的密度显著降低。海马体中mGlu受体密度和蛋白表达的后者降低与[³H]MPEP亲和力增加平行,且与单次腹腔注射可卡因后给予初用配对生理盐水对照组大鼠所观察到的升高相反。此外,我们还观察到两个可卡因组边缘皮质中受试受体的蛋白表达均显著升高。目前的结果显示了mGlu受体定位和膜特异性结合的方式依赖性和脑区特异性变化。