酸枣仁汤通过抑制TLR4/NFκB/NLRP3炎症信号通路调节微生物群肠脑轴,改善抑郁样行为。

IF 2.7 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yiyang Du, Bosai He, Bo Wu, Tingxu Yan, Ying Jia
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引用次数: 0

摘要

抑郁症是一种常见但严重的疾病,给个人和社会带来巨大负担。最近,抑郁症的发生与微生物群-肠-脑轴有关。toll样受体4(TLR4)/核因子κB激酶(NFκB)/NOD样受体热蛋白结构域相关蛋白3(NLRP3)通路与微生物群-肠-脑轴的调节密切相关。酸枣仁汤是汉代《金龟要略》中记载的一种治疗失眠、抑郁的药物,长期以来一直被人们广泛使用。然而,SZRD通过TLR4/NFκB/NLRP3通路调节抑郁症的作用机制尚不清楚。在本研究中,首次在慢性不可预测轻度应激(CUMS)小鼠模型上进行SZRD。行为测试结果表明,SZRD治疗能有效改善CUMS小鼠的抑郁样行为。根据我们以往对SZRD成分的体内外研究,采用超高效液相色谱-四极杆飞行时间质谱法对抑郁症模型大鼠血清代谢产物的鉴定进行了进一步的定性分析。鉴定出27个原型和44个代谢产物。代谢反应主要有葡萄糖醛酸化、硫酸化等。然后,利用免疫组织化学和蛋白质印迹法监测小鼠大脑和结肠中TLR4/NFκB/NLRP3信号通路激活的差异。结果表明,SZRD处理可降低相关因子的表达水平。此外,SZRD治疗还可以抑制海马和结肠通路形态的组织病理学损伤。16SrRNA检测结果表明,SZRD能减轻抑郁小鼠肠道菌群的失调。上述结果为研究SZRD通过抑制TLR4/NFκB/NLRP3通路调节微生物群肠脑轴治疗抑郁症的作用机制提供了重要信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Suanzaoren decoction improves depressive-like behaviors by regulating the microbiota-gut-brain axis via inhibiting TLR4/NFκB/NLRP3 inflammation signal pathway

Suanzaoren decoction improves depressive-like behaviors by regulating the microbiota-gut-brain axis via inhibiting TLR4/NFκB/NLRP3 inflammation signal pathway

Depression is a common but serious sickness which causes a considerable burden on individuals and society. Recently, it has been well established that the occurrence of depression was related to the microbiota-gut-brain axis. The toll-like receptor 4 (TLR4)/ nuclear factor kappa-B kinase (NFκB)/ NOD-like receptor thermal protein domain associated protein 3 (NLRP3) pathway is closely associated with the regulation of microbiota-gut-brain axis. Suanzaoren Decoction (SZRD), which recorded in Jin Gui Yao Lve in Han dynasty, has been used for treating insomnia and depression for a long time. However, the action mechanism of the depression regulation through the TLR4/NFκB/NLRP3 pathway by SZRD was still unclear. In this study, SZRD was firstly performed on a chronic unpredictable mild stress (CUMS) mice model. The results of behavioral tests showed that SZRD treatment could ameliorate the depressive-like behaviors of CUMS mice effectively. According to our previous researches about the components of SZRD in vitro and in vivo, the identification of serum metabolites in depression model rats was further analyzed qualitatively using ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry. 27 prototypes and 44 metabolites were identified. The main types of metabolic reactions are glucuronization, sulfation, and so on. Then, using immunohistochemistry and western blotting to monitor the difference in activation of TLR4/NFκB/NLRP3 signaling pathway in mice brain and colon. The results showed that SZRD treatment could reduce expression levels of related factors. Additionally, the SZRD treatment could also inhibit the histopathological damage in the path morphology of the hippocampus and colon. The results of 16SrRNA demonstrated that SZRD could reduce the dysbiosis of the intestinal flora of depressive mice. The above results provided important information for studying the action mechanism of SZRD in treating depression by regulating microbiota-gut-brain axis via inhibiting TLR4/NFκB/NLRP3 pathway.

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来源期刊
Journal of chemical neuroanatomy
Journal of chemical neuroanatomy 医学-神经科学
CiteScore
4.50
自引率
3.60%
发文量
87
审稿时长
62 days
期刊介绍: The Journal of Chemical Neuroanatomy publishes scientific reports relating the functional and biochemical aspects of the nervous system with its microanatomical organization. The scope of the journal concentrates on reports which combine microanatomical, biochemical, pharmacological and behavioural approaches. Papers should offer original data correlating the morphology of the nervous system (the brain and spinal cord in particular) with its biochemistry. The Journal of Chemical Neuroanatomy is particularly interested in publishing important studies performed with up-to-date methodology utilizing sensitive chemical microassays, hybridoma technology, immunocytochemistry, in situ hybridization and receptor radioautography, to name a few examples. The Journal of Chemical Neuroanatomy is the natural vehicle for integrated studies utilizing these approaches. The articles will be selected by the editorial board and invited reviewers on the basis of their excellence and potential contribution to this field of neurosciences. Both in vivo and in vitro integrated studies in chemical neuroanatomy are appropriate subjects of interest to the journal. These studies should relate only to vertebrate species with particular emphasis on the mammalian and primate nervous systems.
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