Böhm C, Newrzella D, Herberger S, Schramm N, Eisenhardt G, Schenk V, Sonntag-Buck V, Sorgenfrei O
AXARON Bioscience AG, Heidelberg, Germany.
J Neurochem. 2006 Apr;97 Suppl 1:44-9. doi: 10.1111/j.1471-4159.2006.03750.x.
A gene expression study of mice treated with the tricyclic antidepressant amitriptyline was performed. To enable the detection of cell type-specific expression changes, laser-microdissected nucleus accumbens was analysed after 4 and 28 days of treatment. After 4 days of treatment no significantly regulated genes could be detected in this study. In contrast, 95 genes exhibited different expression levels in animals treated for 28 days with amitrityline compared with sham animals. This observation reflects the long-term effects and adaptation processes observed in patients treated with this drug. Among the regulated genes are receptors belonging to the dopamine-dependent signalling cascade, ion channels (mainly voltage-dependent potassium and calcium channels) potentially involved in signalling cascades and neuropeptides. The results support the hypothesis that the therapeutic effect of this antidepressant is much more complex and not confined to a reuptake inhibition of neurotransmitters. Paradigms inducing only weak expression changes, which may be limited to certain cell types within the highly complex brain structure, can therefore be reliably investigated by applying a cell type-specific expression profiling technique based on laser microdissection and subsequent RNA amplification followed by DNA microarray analysis.
对用三环类抗抑郁药阿米替林治疗的小鼠进行了基因表达研究。为了能够检测细胞类型特异性的表达变化,在治疗4天和28天后,对激光显微切割的伏隔核进行了分析。在本研究中,治疗4天后未检测到明显受调控的基因。相比之下,与假手术动物相比,用阿米替林治疗28天的动物中有95个基因表现出不同的表达水平。这一观察结果反映了在用该药物治疗的患者中观察到的长期效应和适应过程。受调控的基因包括属于多巴胺依赖性信号级联反应的受体、可能参与信号级联反应的离子通道(主要是电压依赖性钾通道和钙通道)和神经肽。这些结果支持了这样一种假说,即这种抗抑郁药的治疗效果要复杂得多,并不局限于神经递质的再摄取抑制。因此,通过应用基于激光显微切割、随后的RNA扩增以及DNA微阵列分析的细胞类型特异性表达谱技术,可以可靠地研究仅诱导微弱表达变化的模式,这些变化可能仅限于高度复杂的脑结构内的某些细胞类型。