Pickering Chris, Bergenheim Veronica, Schiöth Helgi B, Ericson Mia
University of Gothenburg, Institute of Neuroscience and Physiology, Section of Psychiatry and Neurochemistry, PO Box 410, SE-40530 Göteborg, Sweden.
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Aug 1;32(6):1521-6. doi: 10.1016/j.pnpbp.2008.05.011. Epub 2008 May 20.
This study investigated GABA signaling following induction of behavioural sensitization to nicotine. Rats were repeatedly injected with saline, nicotine or hexamethonium for 18 days and gene expression was measured with qPCR. Nicotine upregulated GABAA alpha1 subunit expression in the nucleus accumbens (p<0.05) while no changes were observed for GABAA alpha3, alpha4 or alpha5. In the medial prefrontal cortex, no change in expression of the GABAA subunits was observed. We found that nicotine significantly decreased expression of the transporter GAT-1/SLC6A1 (p<0.05) in the medial prefrontal cortex while the expression of the GAT-3/SLC6A11 (p<0.05) transporter was increased in the nucleus accumbens. This provides the first evidence of neuroadaptive changes in the GABA system after nicotine sensitization and the first demonstration of an effect on GAT-1 or GAT-3 transporters in the addiction field. The GAT-1 findings also provide evidence for an alternative theory of why most schizophrenic individuals also use tobacco products.
本研究调查了尼古丁行为敏化诱导后的γ-氨基丁酸(GABA)信号传导。大鼠连续18天反复注射生理盐水、尼古丁或六甲铵,并用定量聚合酶链反应(qPCR)测量基因表达。尼古丁上调了伏隔核中GABAAα1亚基的表达(p<0.05),而GABAAα3、α4或α5未观察到变化。在内侧前额叶皮质,未观察到GABAA亚基表达的变化。我们发现,尼古丁显著降低了内侧前额叶皮质中转运体GAT-1/SLC6A1的表达(p<0.05),而伏隔核中GAT-3/SLC6A11转运体的表达增加(p<0.05)。这为尼古丁敏化后GABA系统的神经适应性变化提供了首个证据,也是成瘾领域中对GAT-1或GAT-3转运体产生影响的首次证明。GAT-1的研究结果也为为何大多数精神分裂症患者也使用烟草制品的另一种理论提供了证据。