百合多糖通过减少ROS的产生来防止四氧嘧啶诱导的HIT-T15细胞损伤

Yuping Li, J. Chang, Cheng-mei Liu, X. Xiong, Y. Gong, Zi-ling Li
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摘要

本课题组等前期研究表明,从百合球茎水提物中提取的两种多糖(LP-1、LP-2)可降低糖尿病模型动物体内空腹血糖浓度。在本研究中,我们研究了LP-1或LP-2对经过氧化损伤的胰腺d细胞肿瘤来源细胞系HIT-T15的影响。分别观察LP-、四氧嘧啶-或两者处理后HIT-T15细胞的细胞活力、胰岛素分泌和细胞内活性氧(ROS)水平。MTT法检测d细胞代谢活性,ELISA法检测胰岛素分泌。采用DCFH-DA荧光分光光度法检测细胞内ROS。LP-1 (>;0.5 mg/ml)或LP-2 (>;与未处理的正常细胞(p为1 mg/ml)相比,0.1 mg/ml可显著提高细胞活力。重要的是,用10 mg/ml LP-2处理的细胞活力几乎恢复到四氧嘧啶未处理的细胞水平,并完全阻止了葡萄糖刺激的胰岛素释放的降低。我们的研究表明,LP-1或LP-2通过清除细胞内ROS水平来减轻四氧嘧啶诱导的HIT-T15细胞的损伤。这些数据也为LP-1或LP-2作为生物活性成分开发新的抗糖尿病药物提供了一些信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lily Polysaccharide Prevents Alloxan-induced HIT-T15 Cell Damage by Reducing ROS Generation
The previous studies of our team and other researchers have shown that two polysaccharides derived from bulbs of lily aqueous extracts (LP-1, LP-2) can decrease fasting blood glucose concentration in diabetic model animal (in vivo). In the present study, we investigated the effects of LP-1 or LP-2 on cultured pancreatic d-cell tumor-derived cell line HIT-T15 that had undergone oxidative damage. The cell viability, insulin secretion, and intracellular reactive oxygen species (ROS) level were investigated in HIT-T15 cells after LP-, alloxan-, or both-treatment, respectively. The metabolic activity of d-cells was determined by MTT assay while the insulin secretion was detected by ELISA technique. Intracellular ROS was detected by fluorescent spectrophotometry using DCFH-DA. The treatment with LP-1 (>; 0.5 mg/ml) or LP-2 (>; 0.1 mg/ml) could significantly elevated the cell viability compared to untreated normal cells (p 1 mg/ml). Importantly, the viability of cells treated with 10 mg/ml LP-2 were almost restored to the levels of alloxan-untreated cells and completely prevented the lowering of glucose-stimulated insulin release. Our investigation suggested that LP-1 or LP-2 reduced the damage of alloxan-induced HIT-T15 cells through scavenging intracellular ROS level. And these data also provide some information when LP-1 or LP-2 is used as a bioactive component for developing a new anti-diabetic agent.
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