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白杨素通过改善氧化应激和内质网应激拮抗胰岛β细胞的脂毒性。

Acacetin antagonized lipotoxicity in pancreatic β-cells via ameliorating oxidative stress and endoplasmic reticulum stress.

机构信息

Department of Biotechnology, School of Food and Biological Engineering, Jiangsu University, Zhenjiang, 212013, Jiangsu, China.

Department of Biochemistry, School of Medicine, Jiangsu University, Zhenjiang, 212013, Jiangsu, China.

出版信息

Mol Biol Rep. 2022 Sep;49(9):8727-8740. doi: 10.1007/s11033-022-07717-2. Epub 2022 Jul 3.

Abstract

PURPOSE

During the pathogenesis and progression of diabetes, lipotoxicity is a major threat to the function and survival of pancreatic β-cells. To battle against the lipotoxicity induced cellular damages, the present study investigated the beneficial effects of acacetin, a natural antioxidant, on free fatty acid (FFA) stressed RINm5F cells and the potential mechanism involved.

MATERIALS AND METHODS

RINm5F cells with or without 1 h pretreatment of acacetin were treated with 0.35 mM sodium palmitate for 24 h. Cell viability, intracellular reactive oxygen species (ROS) level, antioxidant capacity, cellular apoptosis, and endoplasmic reticulum (ER) stress biomarker expression were investigated.

RESULTS

Our experiments demonstrated that acacetin treatment significantly scavenged the intracellular ROS, upregulated the endogenous antioxidant enzymes, and diminished the sub-G DNA fraction in the cells exposed to FFA, suggesting its efficacy against oxidative stress. Meanwhile, acacetin treatment significantly mitigated the overload of intracellular Ca and reduced the pro-apoptotic protein expression in the FFA stimulated cells, and thereby attenuated the ER stress-mediated cell apoptosis. Furthermore, siRNA interference results confirmed that the suppressing of C/EBP-homologous protein (CHOP) was critical to improve FFA-induced reduction in cell viability and ameliorated the ER stress caused by FFA stimulation.

CONCLUSIONS

Acacetin may antagonize lipotoxicity in pancreatic cells by attenuating the oxidative stress and ER stress.

摘要

目的

在糖尿病的发病机制和进展过程中,脂毒性是胰腺β细胞功能和存活的主要威胁。为了对抗脂毒性诱导的细胞损伤,本研究探讨了天然抗氧化剂芹菜素对游离脂肪酸(FFA)应激的 RINm5F 细胞的有益作用及其潜在机制。

材料和方法

用或不用 1 h 芹菜素预处理的 RINm5F 细胞用 0.35 mM 棕榈酸钠处理 24 h。检测细胞活力、细胞内活性氧(ROS)水平、抗氧化能力、细胞凋亡和内质网(ER)应激生物标志物的表达。

结果

我们的实验表明,芹菜素处理可显著清除细胞内 ROS,上调内源性抗氧化酶,并减少 FFA 暴露细胞中的亚 G1 DNA 片段,表明其对氧化应激的疗效。同时,芹菜素处理可显著减轻细胞内 Ca 过载,并降低 FFA 刺激细胞中的促凋亡蛋白表达,从而减轻 ER 应激介导的细胞凋亡。此外,siRNA 干扰结果证实,抑制 C/EBP 同源蛋白(CHOP)对改善 FFA 诱导的细胞活力降低和改善 FFA 刺激引起的 ER 应激至关重要。

结论

芹菜素可能通过减轻氧化应激和内质网应激来拮抗胰腺细胞的脂毒性。

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