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加加减凝胶通过调节甲状腺激素和抑制(白细胞介素-6、肿瘤坏死因子-α、白细胞介素-1β)/Janus激酶2/信号转导和转录激活因子3/血管内皮生长因子途径改善甲状腺结节。

Jiajiejian gel ameliorates thyroid nodules through regulation of thyroid hormones and suppression of the (IL-6, TNF-α, IL-1β)/JAK2/STAT3/VEGF pathway.

作者信息

Wang Changlin, Gao Xiangju, Qiao Mingqi, Gao Dongmei, Guo Yinghui, Wang Jieqiong, Song Chunhong

机构信息

Laboratory Animal Center, Central Hospital Affiliated to Shandong First Medical University, Jinan, China.

School of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.

出版信息

Front Pharmacol. 2024 Oct 18;15:1483686. doi: 10.3389/fphar.2024.1483686. eCollection 2024.

Abstract

BACKGROUND

The high incidence of thyroid nodules and their rapid growth in recent years have become an important issue affecting public health. Traditional Chinese medicine (TCM) external treatments have unique advantages in treating this disease, but the currently available external preparations are relatively few and the therapeutic mechanism is unclear. Jiajiejian gel (JJJG) is a TCM external preparation developed by our team for the thyroid nodule treatment, which has been preliminarily proven to be safe and effective in clinical practice.

OBJECTIVE

The current study was aimed to elucidate the therapeutic effects and the underlying mechanisms of JJJG on thyroid nodules in rats.

METHODS

The contents of paeonol and forsythoside A in JJJG were determined by HPLC. The thyroid nodules rat model was established through oral gavage of 0.1% propylthiouracil (PTU) for 6 weeks and meanwhile the rats were treated with external JJJG (0.26, 0.52, 1.04 g/kg). Subsequently, the therapeutic effect of JJJG was observed by means of ultrasonic examination, morphology observation, organ coefficients determination and histopathological analysis. Mechanismlly, the levels of FT3, FT4 and TSH in serum were measured and transcriptomics methods were used to analyse and screen the key targets and pathways of alleviating thyroid nodules by JJJG. Further, gene and protein expression levels of key factors in the pathways were measured and validated using quantitative real-time PCR, ELISA, western blotting and immunofluorescence, so as to clarify the therapeutic mechanism.

RESULTS

The contents of the paeonol and forsythoside A were 1.160 and 0.608 mg/g, respectively. JJJG reduced thyroid swelling, improved nodular lesions, decreased thyroid coefficients, and inhibited abnormal nodular hyperplasia of follicular epithelial cells. In terms of mechanism, JJJG significantly increased the levels of FT3 and FT4 and decreased TSH level in serum ( < 0.05). Transcriptomics suggested that the (IL-6, TNF-α, IL-1β)/JAK2/STAT3/VEGF pathway may be one of the key mechanisms in the treatment of thyroid nodules by JJJG. Further validation experiments demonstrated that JJJG significantly reduced the mRNA expression and protein content of IL-1β, IL-6 and TNF-α in thyroid tissue, as well as the mRNA expression of JAK2, STAT3 and VEGF and the protein expression of p-JAK2/JAK2, p-STAT3/STAT3 and VEGF ( < 0.05).

CONCLUSION

This study indicates that JJJG efficiently ameliorates thyroid nodules by regulating the levels of FT3, FT4 and TSH in serum and suppressing (IL-6, TNF-α, IL-1β)/JAK2/STAT3/VEGF pathway in thyroid tissue, providing a potential therapeutic approach for thyroid nodules.

摘要

背景

近年来甲状腺结节的高发病率及其快速增长已成为影响公众健康的重要问题。中医外治法在治疗该病方面具有独特优势,但目前可用的外用制剂相对较少,且治疗机制尚不清楚。加节软坚凝胶(JJJG)是我们团队研发的用于治疗甲状腺结节的中药外用制剂,已在临床实践中初步证明其安全有效。

目的

本研究旨在阐明JJJG对大鼠甲状腺结节的治疗作用及其潜在机制。

方法

采用高效液相色谱法测定JJJG中丹皮酚和连翘苷A的含量。通过口服灌胃0.1%丙硫氧嘧啶(PTU)6周建立甲状腺结节大鼠模型,同时对大鼠进行JJJG外用治疗(0.26、0.52、1.04 g/kg)。随后,通过超声检查、形态学观察、脏器系数测定和组织病理学分析观察JJJG的治疗效果。机制上,检测血清中FT3、FT4和TSH水平,并采用转录组学方法分析和筛选JJJG缓解甲状腺结节的关键靶点和通路。进一步,使用定量实时PCR、ELISA、蛋白质免疫印迹和免疫荧光法检测并验证通路中关键因子的基因和蛋白表达水平,以阐明其治疗机制。

结果

JJJG中丹皮酚和连翘苷A的含量分别为1.160和0.608 mg/g。JJJG减轻了甲状腺肿胀,改善了结节性病变,降低了甲状腺系数,并抑制了滤泡上皮细胞的异常结节性增生。在机制方面,JJJG显著提高了血清中FT3和FT4的水平,并降低了TSH水平(P<0.05)。转录组学表明,(IL-6、TNF-α、IL-1β)/JAK2/STAT3/VEGF通路可能是JJJG治疗甲状腺结节的关键机制之一。进一步的验证实验表明,JJJG显著降低了甲状腺组织中IL-1β、IL-6和TNF-α的mRNA表达和蛋白含量,以及JAK2、STAT3和VEGF的mRNA表达和p-JAK2/JAK2、p-STAT3/STAT3和VEGF的蛋白表达(P<0.05)。

结论

本研究表明,JJJG通过调节血清中FT3、FT4和TSH水平以及抑制甲状腺组织中(IL-6、TNF-α、IL-1β)/JAK2/STAT3/VEGF通路有效改善甲状腺结节,为甲状腺结节提供了一种潜在的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f31/11527726/fe24dbf31895/fphar-15-1483686-g001.jpg

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