研究1,8-桉树脑在HFSD/STZ 2型糖尿病模型中减轻铁下垂的作用:GEO数据分析方法。

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Hong Yang, Yongxin Chen, Guoping Wu, Pengyan Ren, Tingting Chen, Jia Liu, Bao Zhang, Xiao Ma, Feng Jiang, Yue Li, Ling Tao, Xiangchun Shen
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引用次数: 0

摘要

山茱萸(FAZ)是中国贵州苗族使用的一种民间草药,富含1,8-桉树脑——一种具有抗氧化和神经保护作用的生物活性单萜氧化物。然而,其治疗胰腺β细胞功能障碍(2型糖尿病(T2DM)的标志)的潜力仍未被探索。本研究探讨了1,8-桉树脑减轻高血糖诱导的β细胞铁下垂的分子机制。采用高脂高糖饮食/链脲佐菌素(HFSD/STZ)诱导2型糖尿病模型(DM)和高糖(HG)处理β细胞模型。我们证明1,8-桉树脑改善了糖尿病小鼠胰岛结构紊乱和病理性糖原沉积。在机制上,1,8-桉树脑抑制脂质过氧化和铁超载,同时恢复铁下垂标志物(GPX4和COX2)的表达。它同时解决了自噬缺陷,表现为LC3II/I比值上调,Beclin-1表达增强,p62稳定。糖尿病胰腺转录组(GEO数据集GSE25724)的生物信息学分析将铁下垂和PI3K/AKT/mTOR信号与β细胞功能障碍联系起来。细胞热移实验(CETSA)和分子对接证实了1,8-桉树脑与PI3K的直接结合,在催化位点具有良好的结合能。利用740-YP (PI3K激动剂YP)和LY294002 (PI3K抑制剂LY)进行药理学验证,发现1,8-桉树脑通过激活PI3K/AKT/mTOR通路发挥其抗铁致死作用。与740-YP共处理可协同增强β细胞的保护作用,而LY294002则会削弱1,8-桉树脑的作用。总的来说,这些发现揭示了1,8-桉树脑作为一种新的PI3K/AKT/mTOR激活剂,通过协调调节自噬和铁凋亡来拯救β细胞的功能,从而为其治疗糖尿病的应用提供了机制基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating the role of 1,8-Cineole in mitigating ferroptosis in a HFSD/STZ diabetes mellitus type 2-induced model: A GEO data analysis approach.

Fructus Alpiniae Zerumbet (FAZ), a folk medicinal herb used by the Miao people in Guizhou, China, is rich in 1,8-Cineole - a bioactive monoterpene oxide with antioxidant and neuroprotective properties. However, its therapeutic potential against pancreatic β cells dysfunction, a hallmark of type 2 diabetes mellitus (T2DM), remains unexplored. This study investigated the molecular mechanism by which 1,8-Cineole mitigates hyperglycemia induced β cells ferroptosis. Using high-fat and high-sugar diet / streptozotocin (HFSD/STZ) diabetes mellitus type 2-induced model (DM) and high glucose (HG)-treated β cells model. We demonstrated that 1,8-Cineole ameliorated pancreatic islet structural disorganization and pathological glycogen deposition in diabetic mice. Mechanistically, 1,8-Cineole suppressed lipid peroxidation and iron overload while restoring the expression of ferroptosis markers (GPX4 and COX2). It concurrently resolved autophagy deficiency, evidenced by upregulated LC3II/I ratio, enhanced Beclin-1 expression, and stabilized p62. Bioinformatic analysis of diabetic pancreatic transcriptomes (GEO dataset GSE25724) linked ferroptosis and PI3K/AKT/mTOR signaling to β cells dysfunction. Cellular thermal shift assay (CETSA) and molecular docking confirmed direct binding of 1,8-Cineole to PI3K with favorable binding energy at the catalytic site. Pharmacological validation using 740-YP (YP, a PI3K agonist) and LY294002 (LY, a PI3K inhibitor) revealed that 1,8-Cineole exerted its anti-ferroptotic effects via PI3K/AKT/mTOR pathway activation. Co-treatment with 740-YP synergistically enhanced β cells protection, whereas LY294002 abrogated 1,8-Cineole's efficacy. Collectively, these findings unveil 1,8-Cineole as a novel PI3K/AKT/mTOR activator that rescues β cells function via coordinated regulation of autophagy and ferroptosis, thereby providing a mechanistic foundation for its therapeutic application in DM.

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来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
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