Dodd Peter R, Buckley S Tracey, Eckert Allison L, Foley Philomena F, Innes David J
School of Molecular and Microbial Science, University of Queensland, Brisbane 4072, Australia.
Ann N Y Acad Sci. 2006 Aug;1074:104-15. doi: 10.1196/annals.1369.010.
Chronic alcohol misuse by human subjects leads to neuronal loss in regions such as the superior frontal cortex (SFC). Propensity to alcoholism is associated with several genes. gamma-Aminobutyric acid (GABA)(A) receptor expression differs between alcoholics and controls, whereas glutamate receptor differences are muted. We determined whether genotype differentiated the regional presentation of GABA(A) and glutamate-NMDA (N-methyl-d-aspartate) receptors in SFC. Autopsy tissue was obtained from alcoholics without comorbid disease, alcoholics with liver cirrhosis, and matched controls. ADH1C, DRD2B, EAAT2, and APOE genotypes modulated GABA(A)-beta subunit protein expression in SFC toward a less-effective form of the receptor. Most genotypes did not divide alcoholics and controls on glutamate-NMDA receptor pharmacology, although gender and cirrhosis did. Genotype may affect amino acid transmission locally to influence neuronal vulnerability.
人类长期滥用酒精会导致前额叶皮质(SFC)等区域的神经元丢失。酗酒倾向与多个基因有关。酗酒者和对照组之间γ-氨基丁酸(GABA)(A)受体的表达存在差异,而谷氨酸受体的差异则不明显。我们确定了基因型是否区分了SFC中GABA(A)和谷氨酸-N-甲基-D-天冬氨酸(NMDA)受体的区域表现。尸检组织取自无合并症的酗酒者、患有肝硬化的酗酒者以及匹配的对照组。乙醇脱氢酶1C(ADH1C)、多巴胺受体D2B(DRD2B)、兴奋性氨基酸转运体2(EAAT2)和载脂蛋白E(APOE)基因型将SFC中GABA(A)β亚基蛋白的表达调节为受体的低效形式。尽管性别和肝硬化会影响,但大多数基因型在谷氨酸-NMDA受体药理学方面并不能区分酗酒者和对照组。基因型可能会局部影响氨基酸传递,从而影响神经元的易损性。