Bakhtazad Atefeh, Vousooghi Nasim, Garmabi Behzad, Zarrindast Mohammad Reza
Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran; Genetics Laboratory, Iranian National Center for Addiction Studies (INCAS), Iranian Institute for Reduction of High-Risk Behaviors, Tehran University of Medical Sciences, Tehran, Iran; Research Center for Cognitive and Behavioral Sciences, Tehran University of Medical Sciences, Tehran, Iran.
Eur J Pharmacol. 2017 May 5;802:52-59. doi: 10.1016/j.ejphar.2017.02.040. Epub 2017 Feb 24.
The importance of Cocaine- and amphetamine-regulated transcript (CART) peptide in reinforcing effects of addictive drugs specially alcohol and psychostimulants has been stablished. Involvement of CART peptide in rewarding effects of opioids in brain has recently been reported. Here we have studied the expression of CART mRNA and peptide in the reward pathway in morphine-induced sensitization phenomenon and also evaluated the peptide level fluctuations in CSF and plasma. Male Wistar rats received 7-day morphine injection (20mg/kg) and then after a 7-day washout period, a challenge dose of 10mg/kg morphine was administered and locomotor activity and oral stereotypical behaviors were recorded. Besides, the expression level of CART mRNA and peptide in four important areas of the mesocorticolimbic reward pathway including nucleus accumbens, striatum, prefrontal cortex, and hippocampus were measured by real-time PCR and western blotting, respectively. The level of the peptide in CSF and plasma was measured by Elisa method. The expression level of CART mRNA and protein in brain regions and also the peptide level in CSF and plasma were significantly down-regulated after 7-day morphine administration. These reduced levels returned to nearly normal rates after 7-day wash-out period. Administration of morphine challenge dose led to significant upregulation of CART gene expression (both mRNA and peptide) in the brain, and elevation of peptide level in CSF and plasma in morphine-sensitized rats. It can be concluded that CART is released in the framework of reward pathway and may serve as an important neurotransmitter in the process of morphine dependence and sensitization.
可卡因和苯丙胺调节转录物(CART)肽在成瘾药物尤其是酒精和精神兴奋剂的强化作用中的重要性已得到确立。最近有报道称CART肽参与了大脑中阿片类药物的奖赏效应。在此,我们研究了吗啡诱导的敏化现象中奖赏通路中CART mRNA和肽的表达,并评估了脑脊液和血浆中肽水平的波动。雄性Wistar大鼠接受7天的吗啡注射(20mg/kg),然后在7天的洗脱期后,给予10mg/kg的吗啡激发剂量,并记录其运动活性和口腔刻板行为。此外,分别通过实时PCR和蛋白质印迹法测量中脑边缘奖赏通路四个重要区域(伏隔核、纹状体、前额叶皮质和海马体)中CART mRNA和肽的表达水平。通过酶联免疫吸附测定法测量脑脊液和血浆中肽的水平。给予吗啡7天后,脑区中CART mRNA和蛋白质的表达水平以及脑脊液和血浆中肽的水平均显著下调。在7天的洗脱期后,这些降低的水平恢复到几乎正常的速率。给予吗啡激发剂量导致吗啡致敏大鼠大脑中CART基因表达(mRNA和肽)显著上调,以及脑脊液和血浆中肽水平升高。可以得出结论,CART在奖赏通路的框架内释放,可能在吗啡依赖和敏化过程中作为一种重要的神经递质。