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

机译:尼古丁与年龄相关的影响在腹侧被盖区和黑质中神经保护基因的表达

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摘要

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.
机译:多巴胺能神经元的选择性变性主要位于中脑的黑质(SN)中,是帕金森氏病(PD)的标志之一。大规模微阵列实验数据揭示了几个基因,在腹侧被盖区(VTA)和SN多巴胺(DA)神经元之间表达明显不同。几项流行病学研究还表明,PD患者中尼古丁介导的神经保护作用。基于有力的证据表明脂蛋白脂肪酶(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作用,这封信调查了这些基因在不同年龄段的VTA和SN中表达的区域和年龄特异性尼古丁调节(3个月,12个月和24个月)在体内动物模型中。我们的体内大鼠模型结果表明,在这些基因中,只有LPL基因在高龄组(24个月)中VTA和SN之间具有明显的差异表达。尼古丁治疗并没有上调成人和老年人组(12和24个月)的神经保护基因。 LPL基因在老年人口中的差异表达可能有助于VTA和SN中DA神经元的不同存活率。但是,尼古丁的下调表明这些基因可能与已知可降低PD风险的尼古丁介导的神经保护作用无关。我们的结果表明,尼古丁可能在神经保护性基因表达的调节中不发挥重要作用,同时为尼古丁在PD中的作用提供了新见解。

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