Modulation of c-Jun N-terminal kinase signaling and specific glucocorticoid receptor phosphorylation in the treatment of major depression

被引:12
作者
Jovicic, Milica J. [1 ]
Lukic, Iva [2 ]
Radojcic, Marija [2 ]
Adzic, Miroslav [2 ]
Maric, Nadja P. [1 ,3 ]
机构
[1] Univ Belgrade, Sch Med, Belgrade 11001, Serbia
[2] Univ Belgrade, Dept Mol Biol & Endocrinol, VINCA Inst Nucl Sci, Belgrade 11001, Serbia
[3] Clin Ctr Serbia, Psychiat Clin, Belgrade 11000, Serbia
关键词
TARGET GENE-EXPRESSION; HPA AXIS; JNK PATHWAY; KAPPA-B; STRESS; INFLAMMATION; ACTIVATION; APOPTOSIS; DISORDER; MECHANISMS;
D O I
10.1016/j.mehy.2015.05.015
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glucocorticoid resistance is a common finding in major depressive disorder. Increased glucocorticoid receptor (GR) phosphorylation at serine 226 is associated with increased glucocorticoid resistance. Previously we have demonstrated that depressed patients exhibit higher levels of GR phosphorylated at serine 226 compared to healthy controls. The enzyme that is involved in this specific GR phosphorylation is c-Jun N-terminal kinase (JNK). We propose that modulation of glucocorticoid phosphorylation at serine 226, by targeting JNK signaling pathway, could be a potential strategy for antidepressant treatment. We base this assumption on the results of previous research that examined GR phosphorylation and JNK signaling in animal models and human studies. We also discuss the potential challenges in targeting JNK signaling pathway in depression. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:291 / 294
页数:4
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