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Serum claudin-5 levels among patients with unipolar and bipolar depression in relation to the pro-inflammatory cytokine tumor necrosis factor-alpha levels

肿瘤坏死因子α 细胞因子 双相情感障碍 重性抑郁障碍 克洛丹 白细胞介素6 萧条(经济学) 炎症 血脑屏障 医学 促炎细胞因子 内科学 免疫学 紧密连接 内分泌学 生物 中枢神经系统 宏观经济学 经济 细胞生物学 扁桃形结构 锂(药物)
作者
Eldar Hochman,Michal Taler,Reut Flug,Shay Gur,Shira Dar,Gil Bormant,Dori Blattberg,Uri Nitzan,Amir Krivoy,Abraham Weizman
出处
期刊:Brain Behavior and Immunity [Elsevier]
卷期号:109: 162-167 被引量:15
标识
DOI:10.1016/j.bbi.2023.01.015
摘要

Accumulating evidence indicates that inflammation and neurovascular unit (NVU) dysfunction contribute to depression via disrupted blood-brain barrier (BBB) integrity. Claudin-5, an endothelial tight-junction protein expressed in the NVU and contributing to BBB integrity, has been implicated in psychiatric disorders, including major depressive disorder (MDD) and schizophrenia. In an animal model of depressive-like behavior, the pro-inflammatory cytokine tumor necrosis factor-alpha (TNF-α) was found to affect BBB permeability and claudin-5 expression of NVU endothelial cells. To the best of the authors' knowledge, this study is the first to assess the relationship between serum claudin-5 and TNF-α levels, during major depressive episodes (MDEs). Serum levels of claudin-5 and TNF-α of 40 patients diagnosed with current MDE [19 with MDD and 21 with bipolar disorder (BD)] and 28 matched healthy controls (HCs) were analyzed. Claudin-5 and TNF-α serum levels in the MDE group were significantly higher than in the HC one. Discrete analysis according to MDE type indicated significantly increased claudin-5 serum levels in BD but not in MDD patients, compared to HCs, even after controlling for confounders. In the MDE group, a significant positive correlation was found between claudin-5 and TNF-α serum levels. In complementary analysis, serum levels of the pro-inflammatory cytokine interleukin-6 were significantly higher among MDE patients compared to HCs, however, no significant correlation was found with claudin-5 levels. In conclusion, as indicated by preclinical studies, our clinical study suggests a possible specific interaction between the NVU/BBB marker claudin-5 and the inflammatory marker TNF-α in the pathogenesis of depression.
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