Revealing the Mechanism of Buzhong Yiqi Tang in Ameliorating Autoimmune Thyroiditis via the Toll-like Receptor Pathway.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Zhuo Zhao, Jiayun Li, Donglin Liu, Hao Gao, Zhe Jin, Zhimin Wang, Yiran Chen, Si Chen, Ziyu Liu, Xiao Yang
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引用次数: 0

Abstract

Objective: Autoimmune thyroiditis (AIT) is one of the most common autoimmune diseases and often causes hypothyroidism in patients. As a traditional formulation in my country, Buzhong Yiqi decoction (BZYQD) has significant effects in improving clinical symptoms of AIT and reducing autoantibody titers, but its specific mechanism of action needs to be further explored. The purpose of this study was to explore the effective targets and related mechanisms of Buzhong Yiqi decoction in AIT mice based on transcriptome sequencing technology.

Methods: Forty NOD.H-2h4 mice were selected and 0.05% NaI was drinking ad libitum for 8 weeks to establish AIT mice, and drug intervention was performed according to groups for 8 weeks. The groups were as follows: control group, Model Group, Buzhong Yiqi Decoction group (9.56 g·kg-1) and Positive control group (Se yeast tablets, 3.033×10-5 g·kg-1), of which Buzhong Yiqi Decoction was the clinical equivalent dose. Thyroid tissues of the Model Group, blank group and Buzhong Yiqi Decoction group were subjected to transcriptome sequencing to analyze the expression of differential genes, and enrichment analysis was carried out. Hematoxylin and eosin staining (HE staining) was used to detect the pathological changes in thyroid tissues, and enzymelinked immunosorbent assay (ELISA) was used to detect the content of serum thyroglobulin antibody (TGAb) to determine the intervention effect of Buzhong Yiqi Decoction; Real-time fluorescence quantitative polymerase chain reaction (Real-time PCR) was performed based on the transcriptome sequencing results to detect the expression of TLR8, JUN, TICAM2, TIRAP, and IL-1β mRNA in thyroid tissue.

Results: According to the transcriptome results, compared with the blank group, there were 327 significantly up-regulated genes and 440 significantly down-regulated genes in the Model Group; compared with the Model Group, there were 502 significantly up-regulated genes and 380 significantly down-regulated genes in the Buzhong Yiqi Decoction group, mainly enriched in immune inflammation and other related pathways including Toll-like receptors. Animal experiments showed that compared with the control group, the model group had obvious lymphocyte infiltration in thyroid tissue under light microscope, a significant increase in inflammatory cells, a significant increase in TGAb content in serum, and a significant increase in TLR8, JUN, TICAM2, TIRAP, IL-1β mRNA expression was observed (P<0.05 or P<0.01). Compared with the Model Group, Buzhong Yiqi Decoction could significantly improve the inflammatory damage of thyroid tissue in AIT mice, reduce the content of TGAb in serum, and down-regulate the expression of TLR8, JUN, TICAM2, TIRAP, IL-1β mRNA (P<0.05 or P<0.01).

Conclusion: Buzhong Yiqi Decoction can effectively improve the inflammatory damage of AIT, and inhibiting the abnormal activation of the Toll-like receptor pathway may be one of its intervention mechanisms.

补中益气汤通过toll样受体途径改善自身免疫性甲状腺炎的机制
目的:自身免疫性甲状腺炎(AIT)是最常见的自身免疫性疾病之一,常引起甲状腺功能减退。补中益气汤(BZYQD)作为我国传统方剂,对改善AIT临床症状、降低自身抗体滴度有显著作用,但其具体作用机制有待进一步探讨。本研究旨在基于转录组测序技术,探讨补中益气汤对AIT小鼠的作用靶点及相关机制。方法:选取40只NOD.H-2h4小鼠,给予0.05% NaI随意灌胃8周,建立AIT小鼠,并按组进行药物干预,疗程8周。各组分为:对照组、模型组、补中益气汤组(9.56 g·kg-1)和阳性对照组(酵母硒片,3.033×10-5 g·kg-1),其中补中益气汤为临床等量剂量。对模型组、空白组和补中益气汤组甲状腺组织进行转录组测序,分析差异基因的表达,并进行富集分析。采用苏木精伊红染色(HE)检测大鼠甲状腺组织的病理变化,采用酶联免疫吸附法(ELISA)检测血清甲状腺球蛋白抗体(TGAb)含量,以确定补中益气汤的干预效果;基于转录组测序结果,采用实时荧光定量聚合酶链反应(Real-time PCR)检测甲状腺组织中TLR8、JUN、TICAM2、TIRAP和IL-1β mRNA的表达。结果:转录组结果显示,与空白组比较,模型组有327个基因显著上调,440个基因显著下调;与模型组比较,补中益气汤组有502个基因显著上调,380个基因显著下调,主要富集于免疫炎症及toll样受体等相关通路。动物实验显示,与对照组相比,光镜下模型组大鼠甲状腺组织淋巴细胞明显浸润,炎性细胞明显增多,血清中TGAb含量明显升高,TLR8、JUN、TICAM2、TIRAP、IL-1β mRNA表达明显升高(p)。补中益气汤能有效改善AIT炎症损伤,抑制toll样受体通路异常激活可能是其干预机制之一。
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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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