Bliźniewska-Kowalska Katarzyna, Gałecki Piotr, Su Kuan-Pin, Halaris Angelos, Szemraj Janusz, Gałecka Małgorzata
Department of Adult Psychiatry, Medical University of Lodz, 91-229 Lodz, Poland.
College of Medicine, China Medical University, Taichung 404, Taiwan.
J Clin Med. 2022 Jun 9;11(12):3321. doi: 10.3390/jcm11123321.
Taking into account the role of oxidative stress in neurodegeneration, we sought to evaluate the expression of genes for select enzymes with antioxidant properties (paraoxonases PON1, PON2 and PON3 and myeloperoxidase MPO) at the mRNA and protein levels in patients with depressive disorders. We further sought to determine the impact of oxidative stress in the etiopathogenesis of this group of mood disorders. A total of 290 subjects (190 depressed patients, 100 healthy controls) took part in the study. Sociodemographic and clinical data were collected. The severity of depressive symptoms was assessed using the Hamilton Depression Rating Scale (HDRS). Venous blood was collected. RT-PCR was used to assess gene expression at the mRNA level, while enzyme-linked immunosorbent assay (ELISA) was used to assess gene expression at the protein level. The expression of the PON2 and PON3 genes at the protein level was significantly higher in depressive patients than in healthy controls. mRNA expression of the PON1, PON2 and PON3 genes was slightly higher in patients with depressive disorders than in the control group, however, this relationship was not statistically significant. On the other hand, the expression of the MPO gene at both mRNA and protein levels was significantly lower in patients with depressive disorder than in the control group. Our results are not in agreement with many studies on enzymes involved in maintaining oxidative balance. Our findings may not support the utility of paraoxonases (PON) or myeloperoxidase (MPO) as promising biomarker candidates of depression pending larger and well controlled studies.
考虑到氧化应激在神经退行性变中的作用,我们试图评估具有抗氧化特性的特定酶(对氧磷酶PON1、PON2和PON3以及髓过氧化物酶MPO)的基因在抑郁症患者mRNA和蛋白质水平的表达。我们进一步试图确定氧化应激在这组情绪障碍病因学中的影响。共有290名受试者(190名抑郁症患者,100名健康对照)参与了该研究。收集了社会人口统计学和临床数据。使用汉密尔顿抑郁量表(HDRS)评估抑郁症状的严重程度。采集静脉血。RT-PCR用于评估mRNA水平的基因表达,而酶联免疫吸附测定(ELISA)用于评估蛋白质水平的基因表达。抑郁症患者中PON2和PON3基因的蛋白质水平表达显著高于健康对照。抑郁症患者中PON1、PON2和PON3基因的mRNA表达略高于对照组,然而,这种关系无统计学意义。另一方面,抑郁症患者中MPO基因的mRNA和蛋白质水平表达均显著低于对照组。我们的结果与许多关于参与维持氧化平衡的酶的研究不一致。在进行更大规模且严格对照的研究之前,我们的发现可能不支持将对氧磷酶(PON)或髓过氧化物酶(MPO)作为有前景的抑郁症生物标志物候选物。