The Age-Related Effect of Nicotine on the Expression of Neuroprotective Genes in Ventral Tegmental Area and Substantia Nigra

Pinar Kanlikilicer;Andrei Dragomir;Die Zhang;Yasemin Akay;Metin Akay
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引用次数: 1

Abstract

Selective degeneration of dopaminergic neurons, which are predominantly located in the substantia nigra (SN) of the midbrain, is one of the hallmarks of Parkinson's disease (PD). Large-scale microarray experimental data revealed several genes with significantly differential expression between the ventral tegmental area (VTA) and the SN dopamine (DA) neurons. Several epidemiological studies have additionally indicated nicotine-mediated neuroprotection in PD patients. Based on the strong evidence implicating lipoprotein lipase (LPL), pituitary adenylate cyclase-activating polypeptide and gastrin-releasing peptide genes in neuroprotection, this letter investigates areaand age-specific nicotine regulation of these genes' expression in the VTA and SN of different age groups (3 months, 12 months, and 24 months) in an in vivo animal model. Our in vivo rat model results suggest that out of these genes, only the LPL gene has significantly differential expression between the VTA and SN in the senior age group (24 months). Nicotine treatment did not upregulate the neuroprotective genes in adult and senior groups (12 and 24 months). Differential expression of the LPL gene in the senior population may contribute to the different survival rates of DA neurons within the VTA and SN. However, downregulation by nicotine suggests that these genes may not be related to the nicotine-mediated neuroprotection known to reduce the risks of PD. Our results suggest that nicotine may not play an important role in the regulation of neuroprotective gene expressions, while providing new insights into the role of nicotine in PD.
尼古丁对腹节区和黑质神经保护基因表达的年龄相关性影响
多巴胺能神经元的选择性变性是帕金森病(PD)的特征之一,多巴胺能神经元主要位于中脑黑质(SN)。大规模微阵列实验数据显示,腹侧被盖区(VTA)和SN多巴胺(DA)神经元之间有几个基因表达显著差异。一些流行病学研究还表明,尼古丁介导的帕金森病患者的神经保护作用。基于脂蛋白脂酶(LPL)、垂体腺苷酸环化酶激活多肽和胃泌素释放肽基因参与神经保护的有力证据,本文在体内动物模型中研究了这些基因在不同年龄组(3个月、12个月和24个月)的VTA和SN中表达的区域和年龄特异性尼古丁调节。我们的体内大鼠模型结果表明,在这些基因中,只有LPL基因在老年组(24个月)的VTA和SN之间具有显著差异表达。尼古丁治疗未上调成年组和老年组(12个月和24个月)的神经保护基因。LPL基因在老年人群中的差异表达可能导致VTA和SN中DA神经元的存活率不同。然而,尼古丁的下调表明,这些基因可能与已知的尼古丁介导的降低PD风险的神经保护作用无关。我们的研究结果表明,尼古丁可能在神经保护基因表达的调节中不起重要作用,同时为尼古丁在帕金森病中的作用提供了新的见解。
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