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转录组学和蛋白质组学研究通过来自……的极性环烯醚萜鉴定出大鼠甲状腺功能亢进管理的PI3K-akt通路靶点。

Transcriptomic and proteomic investigations identify PI3K-akt pathway targets for hyperthyroidism management in rats via polar iridoids from .

作者信息

Zhang Ning, Liu Shumin, Lu Xu, Li Zihui, Li Ling, Ye Tao

机构信息

The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang, Guizhou, China.

Institute of Traditional Medicine, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.

出版信息

Heliyon. 2024 Jun 14;10(12):e33072. doi: 10.1016/j.heliyon.2024.e33072. eCollection 2024 Jun 30.

Abstract

High-polarity iridoids from () offer a range of benefits, including anti-inflammatory, antioxidant, antitumour, antibacterial, antiviral, and antiallergic effects. Although previous studies have indicated the potential of for hyperthyroidism prevention and treatment, the specific active compounds involved and their mechanisms of action are not fully understood. This study explored the effects of high-polarity iridoid glycosides from on hyperthyroidism induced in rats by levothyroxine sodium. The experimental design included a control group, a hyperthyroidism model group, and a group treated with iridoid glycosides. Serum triiodothyronine (T3) and thyroxine (T4) levels were quantified using an enzyme-linked immunosorbent assay (ELISA). Transcriptomic and proteomic analyses were applied to liver samples to identify differentially expressed genes and proteins. These analyses were complemented by trend analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. The effectiveness of key factors was further examined through molecular biology techniques. ELISA results indicated a notable increase in T3 and T4 in the hyperthyroid rats, which was significantly mitigated by treatment with iridoid glycosides. Transcriptomic analysis revealed 6 upregulated and 6 downregulated genes in the model group, showing marked improvement following treatment. Proteomic analysis revealed changes in 30 upregulated and 50 downregulated proteins, with improvements observed upon treatment. The PI3K-Akt signalling pathway was investigated through KEGG enrichment analysis. Molecular biology methods verified the upregulation of Spp1, Thbs1, PI3K, and Akt in the model group, which was reversed in the treatment group. This study revealed that highly polar iridoids from can modulate the Spp1 gene and Thbs1 protein via the PI3K-Akt signalling pathway, suggesting a therapeutic benefit for hyperthyroidism and providing a basis for drug development targeting this condition.

摘要

来自()的高极性环烯醚萜具有一系列益处,包括抗炎、抗氧化、抗肿瘤、抗菌、抗病毒和抗过敏作用。尽管先前的研究表明()在预防和治疗甲状腺功能亢进方面具有潜力,但具体涉及的活性化合物及其作用机制尚未完全明确。本研究探讨了来自()的高极性环烯醚萜苷对左甲状腺素钠诱导的大鼠甲状腺功能亢进的影响。实验设计包括对照组、甲状腺功能亢进模型组和环烯醚萜苷治疗组。使用酶联免疫吸附测定(ELISA)定量血清三碘甲状腺原氨酸(T3)和甲状腺素(T4)水平。对肝脏样本进行转录组学和蛋白质组学分析,以鉴定差异表达的基因和蛋白质。这些分析通过趋势分析和京都基因与基因组百科全书(KEGG)富集分析进行补充。通过分子生物学技术进一步检测关键因子的有效性。ELISA结果表明,甲状腺功能亢进大鼠的T3和T4显著升高,而环烯醚萜苷治疗可显著缓解。转录组分析显示模型组中有6个基因上调和6个基因下调,治疗后有明显改善。蛋白质组分析显示30种上调蛋白和50种下调蛋白发生变化,治疗后有所改善。通过KEGG富集分析研究了PI3K-Akt信号通路。分子生物学方法证实模型组中Spp1、Thbs1、PI3K和Akt上调,而治疗组则相反。本研究表明,来自()的高极性环烯醚萜可通过PI3K-Akt信号通路调节Spp1基因和Thbs1蛋白,提示其对甲状腺功能亢进具有治疗作用,并为针对该病症的药物开发提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ed1/11238048/a225ba356b5b/gr1.jpg

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