Sun Dongxiao, Huang Weihua, Hwang Yoon Y, Zhang Yuan, Zhang Qin, Li Ming D
Section of Neurobiology, Department of Psychiatric Medicine, University of Virginia, Charlottesville, VA 22911, USA.
Neuropsychopharmacology. 2007 Jan;32(1):110-6. doi: 10.1038/sj.npp.1301134. Epub 2006 Jun 21.
Our previous genetic studies demonstrated that variants of the gamma-Aminobutyric acid B receptor subunit 2 (GPR51) and neurotrophic tyrosine kinase receptor type 2 (NTRK2) genes are significantly associated with nicotine dependence (ND) in smokers. However, whether such genetic associations lead to changes in the expression of the two genes in response to nicotine remains undetermined. In this study, we investigated the regulatory effect of nicotine on the expression of Gpr51 and Ntrk2 in seven rat brain regions during the administration of nicotine in a daily dose of 3.15 mg/kg for 7 days. With quantitative real-time RT-PCR, we found that nicotine increased the mRNA of Gpr51 by 70, 78, and 32% in the amygdala, striatum, and prefrontal cortex (PFC), respectively, but decreased by 54% in the nucleus accumbens (NA). The Gpr51 protein was upregulated by nicotine in the amygdala (26%), striatum (73%), PFC (28%), and medial basal hypothalamus (MBH; 19%) but downregulated in the NA (-72%). Similarly, the mRNA level of Ntrk2 was enhanced by nicotine in the striatum (86%) and PFC (38%), but decreased in the NA (-46%) and ventral tegmental area (VTA; -49%). A significant change in protein expression was also obtained for Ntrk2 in the PFC (24%), MBH (33%), NA (-33%), and VTA (-70%). Interestingly, these two genes showed a closely coordinated expression pattern in response to nicotine in most of the brain regions examined. In summary, our results demonstrate that the expression of Gpr51 and Ntrk2 is significantly regulated by nicotine at both the mRNA and protein levels in various brain regions, which provides further evidence that these two genes are involved in the etiology of ND, as reported in our previous genetic association studies in humans.
我们之前的遗传学研究表明,γ-氨基丁酸B受体亚基2(GPR51)基因和神经营养性酪氨酸激酶受体2(NTRK2)基因的变体与吸烟者的尼古丁依赖(ND)显著相关。然而,这种基因关联是否会导致这两个基因在尼古丁作用下表达发生变化仍未确定。在本研究中,我们以每日3.15 mg/kg的剂量给大鼠注射尼古丁,持续7天,研究尼古丁对大鼠七个脑区中Gpr51和Ntrk2表达的调节作用。通过定量实时RT-PCR,我们发现尼古丁使杏仁核、纹状体和前额叶皮质(PFC)中的Gpr51 mRNA分别增加了70%、78%和32%,但在伏隔核(NA)中降低了54%。尼古丁使杏仁核(26%)、纹状体(73%)、PFC(28%)和内侧基底下丘脑(MBH;19%)中的Gpr51蛋白上调,但在NA中下调(-72%)。同样,尼古丁使纹状体(86%)和PFC(38%)中的Ntrk2 mRNA水平升高,但在NA(-46%)和腹侧被盖区(VTA;-49%)中降低。Ntrk2在PFC(24%)、MBH(33%)、NA(-33%)和VTA(-70%)中的蛋白表达也有显著变化。有趣的是,在大多数检测的脑区中,这两个基因在对尼古丁的反应中表现出密切协调的表达模式。总之,我们的结果表明,在各个脑区中,Gpr51和Ntrk2的表达在mRNA和蛋白水平上均受到尼古丁的显著调节,这为这两个基因参与尼古丁依赖的病因提供了进一步证据,正如我们之前在人类中的遗传关联研究所报道的那样。