Based on SIRT1/NF-κB/NLRP3 Signal Pathway to Explore the Effect of Yiqi Huatan Huoxue Recipe on Inflammatory Injury in AIT Mice by Pyroptosis.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Zhuo Zhao, Ziyu Liu, Nan Song, Huimin Cao, Yiran Chen, Si Chen, Zhimin Wang, Zhe Jin, Xiao Yang
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引用次数: 0

Abstract

Objective: Autoimmune thyroiditis (AIT) is the most common autoimmune thyroid disease. In recent decades, its incidence and prevalence have sharply increased. Yiqi Huatan Huoxue recipe is a traditional Chinese medicine formula we use to treat AIT. Its clinical efficacy is clear, but the specific mechanism remains unclear. This study aims to explore whether pyroptosis mediated by the SIRT1/NF-κB/NLRP3 signaling pathway is one of the therapeutic mechanisms of Yiqi Huatan Huoxue recipe.

Methods: Forty 8-week-old female NOD.H-2h4 mice were randomly divided into four groups: the normal group (NG), model group (MG), Yiqi Huatan Huoxue recipe group (YG), and western medicine group (selenium yeast tablet, SeG). The normal group was gavaged with distilled water, while the remaining groups were gavaged with 0.05% sodium iodide (NaI) solution for 8 weeks. After the AIT animal model formed naturally, the mice were euthanized by gavage after 8 weeks. Hematoxylin-eosin staining was used to observe thyroid tissue changes, and enzymelinked immunosorbent assay (ELISA) was used to detect serum anti-thyroglobulin antibodies (TGAb) and mouse anti-thyroid peroxidase antibodies (TPOAb). Real-time quantitative PCR (qRT-PCR), Western blot, and immunohistochemistry were used to detect the expression of sirtuin 1 (SIRT1), nuclear factor κB p65 (NF-κB p65), nod-like receptor protein 3 (NLRP3), apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), caspase- 1, gasdermin D (GSDMD), and interleukin (IL)-1β in thyroid tissue.

Results: Compared with the NG group, the thyroid structure of rats in the MG group was severely damaged, with significant lymphocyte infiltration, significantly increased serum TGAb and TPOAb levels, and significantly increased expression levels of SRIT1, NF-κB p65, NLRP3, ASC, Caspase-1, GSDMD, IL-1β mRNA, and protein. Compared with the MG group, the thyroid structure damage and lymphocyte infiltration in rats of each treatment group were improved, and the serum TGAb, TPOAb, SRIT1, NF-κB p65, NLRP3, ASC, Caspase-1, GSDMD, IL-1β mRNA, and protein expression levels were significantly reduced.

Conclusion: Yiqi Huatan Huoxue recipe can alleviate thyroid structural damage in AIT mice, and its mechanism may be related to the upregulation of SIRT1, NF-κB deacetylation, and inhibition of NLRP3-mediated pyroptosis.

基于SIRT1/NF-κB/NLRP3信号通路探讨益气化痰方对AIT小鼠炎症损伤的热休克作用
目的:自身免疫性甲状腺炎(AIT)是最常见的自身免疫性甲状腺疾病:自身免疫性甲状腺炎(AIT)是最常见的自身免疫性甲状腺疾病。近几十年来,其发病率和患病率急剧上升。益气化痰汤是我们用来治疗自身免疫性甲状腺炎的传统中药配方。其临床疗效明确,但具体机制尚不清楚。本研究旨在探讨SIRT1/NF-κB/NLRP3信号通路介导的热蛋白沉积是否是益气化瘀方的治疗机制之一:将40只8周龄雌性NOD.H-2h4小鼠随机分为四组:正常组(NG)、模型组(MG)、益气化瘀方(YG)和西药组(硒酵母片,SeG)。正常组用蒸馏水灌胃,其余各组用 0.05% 碘化钠(NaI)溶液灌胃 8 周。AIT 动物模型自然形成后,小鼠在 8 周后被灌胃安乐死。采用苏木精-伊红染色观察甲状腺组织变化,酶联免疫吸附试验(ELISA)检测血清抗甲状腺球蛋白抗体(TGAb)和小鼠抗甲状腺过氧化物酶抗体(TPOAb)。采用实时定量 PCR(qRT-PCR)、Western 印迹和免疫组织化学方法检测甲状腺组织中 sirtuin 1(SIRT1)、核因子 κB p65(NF-κB p65)、类结节受体蛋白 3(NLRP3)、含 caspase 招募结构域的凋亡相关斑点样蛋白(ASC)、caspase-1、gasdermin D(GSDMD)和白细胞介素(IL)-1β的表达。结果与NG组相比,MG组大鼠甲状腺结构受损严重,淋巴细胞浸润明显,血清TGAb和TPOAb水平显著升高,SRIT1、NF-κB p65、NLRP3、ASC、Caspase-1、GSDMD、IL-1β mRNA和蛋白表达水平显著升高。与MG组相比,各治疗组大鼠的甲状腺结构损伤和淋巴细胞浸润均得到改善,血清TGAb、TPOAb、SRIT1、NF-κB p65、NLRP3、ASC、Caspase-1、GSDMD、IL-1β mRNA和蛋白表达水平均显著降低:结论:益气化痰方能缓解AIT小鼠甲状腺结构损伤,其机制可能与上调SIRT1、NF-κB去乙酰化、抑制NLRP3介导的热蛋白沉积有关。
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来源期刊
CiteScore
3.10
自引率
5.60%
发文量
327
审稿时长
7.5 months
期刊介绍: Combinatorial Chemistry & High Throughput Screening (CCHTS) publishes full length original research articles and reviews/mini-reviews dealing with various topics related to chemical biology (High Throughput Screening, Combinatorial Chemistry, Chemoinformatics, Laboratory Automation and Compound management) in advancing drug discovery research. Original research articles and reviews in the following areas are of special interest to the readers of this journal: Target identification and validation Assay design, development, miniaturization and comparison High throughput/high content/in silico screening and associated technologies Label-free detection technologies and applications Stem cell technologies Biomarkers ADMET/PK/PD methodologies and screening Probe discovery and development, hit to lead optimization Combinatorial chemistry (e.g. small molecules, peptide, nucleic acid or phage display libraries) Chemical library design and chemical diversity Chemo/bio-informatics, data mining Compound management Pharmacognosy Natural Products Research (Chemistry, Biology and Pharmacology of Natural Products) Natural Product Analytical Studies Bipharmaceutical studies of Natural products Drug repurposing Data management and statistical analysis Laboratory automation, robotics, microfluidics, signal detection technologies Current & Future Institutional Research Profile Technology transfer, legal and licensing issues Patents.
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