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炎症性肠病中选定的睡眠参数、抑郁、抗肿瘤坏死因子治疗与脑源性神经营养因子通路之间的关系

Relation between Selected Sleep Parameters, Depression, Anti-Tumor Necrosis Factor Therapy, and the Brain-Derived Neurotrophic Factor Pathway in Inflammatory Bowel Disease.

作者信息

Sochal Marcin, Ditmer Marta, Binienda Agata, Gabryelska Agata, Białasiewicz Piotr, Talar-Wojnarowska Renata, Fichna Jakub, Małecka-Wojciesko Ewa

机构信息

Department of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, 90-419 Lodz, Poland.

Department of Biochemistry, Medical University of Lodz, 90-419 Lodz, Poland.

出版信息

Metabolites. 2023 Mar 19;13(3):450. doi: 10.3390/metabo13030450.

Abstract

Inflammatory bowel disease (IBD) patients often have sleep and mood disorders. Brain-derived neurotrophic factor (BDNF) and proBDNF were shown to modulate interactions between the central nervous system and the gastrointestinal tract, possibly contributing to psychological issues. Anti-tumor necrosis factor (TNF) therapy in IBD can alter BDNF expression and further affect the brain-gut axis. Eighty IBD patients and 44 healthy controls (HCs) were enrolled and divided into subsets based on disease activity and condition (ulcerative colitis (UC)/Crohn's disease (CD)). Questionnaires evaluating sleep parameters and depression as well as venous blood were collected. The IBD group had a lower expression of BDNF mRNA, but higher proBDNF and BDNF protein concentration than HCs. The UC group had a higher BDNF protein concentration than the CD. BDNF protein was positively correlated to sleep efficiency in the IBD group. Depression severity was associated positively with BDNF mRNA and negatively with BDNF protein in the remission group. Anti-TNF therapy enhanced BDNF mRNA expression. The BDNF pathway might be disturbed in IBD, linking it to sleep disorders and depression. Systemic inflammation could be the main cause of this disruption. BDNF mRNA is a more reliable parameter than protein due to numerous post-translational modifications.

摘要

炎症性肠病(IBD)患者常伴有睡眠和情绪障碍。脑源性神经营养因子(BDNF)和前体BDNF已被证明可调节中枢神经系统与胃肠道之间的相互作用,这可能是导致心理问题的原因之一。IBD患者接受抗肿瘤坏死因子(TNF)治疗可改变BDNF表达,并进一步影响脑-肠轴。本研究纳入了80例IBD患者和44例健康对照(HC),并根据疾病活动度和病情(溃疡性结肠炎(UC)/克罗恩病(CD))将其分为不同亚组。收集了评估睡眠参数和抑郁情况的问卷以及静脉血样。IBD组BDNF mRNA表达较低,但前体BDNF和BDNF蛋白浓度高于HC组。UC组BDNF蛋白浓度高于CD组。IBD组中BDNF蛋白与睡眠效率呈正相关。在缓解期组中,抑郁严重程度与BDNF mRNA呈正相关,与BDNF蛋白呈负相关。抗TNF治疗可增强BDNF mRNA表达。BDNF信号通路在IBD中可能受到干扰,从而导致睡眠障碍和抑郁。全身炎症可能是这种干扰的主要原因。由于存在大量翻译后修饰,BDNF mRNA比蛋白更可靠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddc/10056410/a368e0cbfe63/metabolites-13-00450-g001.jpg

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