The role of urokinase, T-cadherin and adiponetin in the development of endogenous depressive disorders

D. Sheleg, M. Karagyaur, A. Primak, E. A. Neyfeld
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Abstract

Introduction The prevalence of depression averages approximately 6 % of the total population. The heritability of depression ranges from 28 % to 44 %. Genetic predisposition may be due to polymorphisms of genes involved in the processes of functioning and morphogenesis of the brain: the balance of monoamines, the action of navigational molecules and their receptors.Purpose of the study To determine the role of genes that regulate the processes of nerve cell migration and directed growth of nerve fibers of navigation receptors (PLAUR and CDH13) or their ligands (PLAU, PLAT, ADIPOQ) in the development of endogenous depression and schizophrenia in the Russian population.Materials and methods At the first stage of the study, the scientific literature was searched in the MEDLINE database. The primary prevalence of genomic variants will be established using whole genome sequencing of 20 patients with severe forms of schizophrenia and endogenous depression. Further, at least 100 patients in each group and 100 healthy donors will take part in the study.Results and discussion The urokinase receptor (uPAR) is involved in neurogenesis by regulating the trajectory of axonal growth. The level of suPAR in blood plasma can act as a biomarker of mild inflammation underlying the etiology of depression. The level of suPAR in plasma can be considered a predictor of the effectiveness of combination therapy with antidepressants and anti-inflammatory drugs. Molecules of the cadherin superfamily are involved in the development of the nervous system, the transmission of intercellular signals, and the regulation of neuronal plasticity. Polymorphisms of the CDH7, CDH9, CDH13, CDH17 genes demonstrate a correlation with the presence of depression. Adiponectin is a hormone secreted by adipose tissue. One of the adiponectin receptors, AdipoR2, stimulates neuronal plasticity and inhibits inflammation and oxidative stress. Plasma concentrations of adiponectin are reduced in depressed patients.Conclusion The results accumulated by researchers testify in favor of the important role of uPAR and T-cadherin in the processes of brain development, and most importantly, in the pathogenesis of the development of endogenous depressions.
尿激酶、t -钙粘蛋白和脂联素在内源性抑郁症发展中的作用
抑郁症的患病率平均约占总人口的6%。抑郁症的遗传率从28%到44%不等。遗传易感性可能是由于参与大脑功能和形态发生过程的基因多态性:单胺的平衡,导航分子及其受体的作用。研究目的探讨俄罗斯人群内源性抑郁症和精神分裂症发生过程中调节神经细胞迁移过程和导航受体(PLAUR和CDH13)或其配体(PLAU、PLAT、ADIPOQ)神经纤维定向生长的基因的作用。材料和方法在研究的第一阶段,在MEDLINE数据库中检索科学文献。基因组变异的主要流行率将通过对20例重度精神分裂症和内源性抑郁症患者的全基因组测序来确定。此外,每组至少有100名患者和100名健康捐赠者将参与这项研究。结果与讨论尿激酶受体(uPAR)通过调节神经轴突生长轨迹参与神经发生。血浆中suPAR的水平可以作为抑郁症病因的轻度炎症的生物标志物。血浆中suPAR的水平可以被认为是抗抑郁药和抗炎药联合治疗有效性的一个预测指标。钙粘蛋白超家族的分子参与神经系统的发育、细胞间信号的传递和神经元可塑性的调节。CDH7、CDH9、CDH13、CDH17基因多态性与抑郁症存在相关性。脂联素是一种由脂肪组织分泌的激素。其中一种脂联素受体AdipoR2可以刺激神经元的可塑性,抑制炎症和氧化应激。抑郁症患者血浆脂联素浓度降低。结论研究人员积累的结果支持了uPAR和T-cadherin在大脑发育过程中的重要作用,最重要的是在内源性抑郁症的发病机制中发挥了重要作用。
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