Iwamoto Kazuya, Bundo Miki, Yamamoto Megumi, Ozawa Hiroki, Saito Toshikazu, Kato Tadafumi
Laboratory for Molecular Dynamics of Mental Disorders, Brain Science Institute, RIKEN, Wako, Saitama 351-0198, Japan.
Neurosci Res. 2004 Aug;49(4):379-85. doi: 10.1016/j.neures.2004.04.002.
Patients with alcoholism exhibit behavioral adaptations to ethanol such as tolerance, dependence, and addiction. Molecular mechanisms that underlie these altered behavioral responses to ethanol are largely unclear. We have performed oligonucleotide microarray analysis in postmortem prefrontal cortices of alcoholics. Among about 12,000 genes represented on microarray, a total of 79 genes showed differential expression changes in alcoholics compared with control subjects, consisting of 54 up- and 25 down-regulated genes. Altered expressions in alcoholics were observed in genes having a wide range of biological functions. The remarkable findings were up-regulation of myelin-related genes and molecular chaperones in alcoholics. Among the genes identified, decreased expressions of NEFH and PCP4/PEP19 were further examined. NEFH encodes a component of neurofilament protein in neurons. PCP4/PEP19 encodes protein involved in calcium signaling and neuronal apoptosis. Observation of their down-regulations in alcoholics in microarray analysis was confirmed by real-time quantitative RT-PCR, and was also confirmed in the independent set of postmortem brains of alcoholics. The present results may provide some insights into understanding the mechanism of ethanol-induced altered behavioral responses at the molecular level.
酗酒患者表现出对乙醇的行为适应性,如耐受性、依赖性和成瘾性。这些对乙醇改变的行为反应背后的分子机制在很大程度上尚不清楚。我们对酗酒者死后的前额叶皮质进行了寡核苷酸微阵列分析。在微阵列上代表的约12000个基因中,与对照受试者相比,共有79个基因在酗酒者中表现出差异表达变化,其中包括54个上调基因和25个下调基因。在具有广泛生物学功能的基因中观察到酗酒者的表达改变。显著的发现是酗酒者中髓鞘相关基因和分子伴侣的上调。在鉴定出的基因中,进一步研究了NEFH和PCP4/PEP19的表达降低情况。NEFH编码神经元中神经丝蛋白的一个成分。PCP4/PEP19编码参与钙信号传导和神经元凋亡的蛋白质。微阵列分析中观察到它们在酗酒者中的下调通过实时定量RT-PCR得到证实,并且在另一组独立的酗酒者死后大脑中也得到了证实。目前的结果可能为在分子水平上理解乙醇诱导的行为反应改变的机制提供一些见解。