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牡荆素-2”-O-鼠李糖苷和牡荆素-4”-O-葡萄糖苷对人脂肪来源干细胞生长及氧化应激诱导细胞凋亡的影响

Effects of vitexin-2"-O-rhamnoside and vitexin-4"-O-glucoside on growth and oxidative stress-induced cell apoptosis of human adipose-derived stem cells.

作者信息

Wei Wenjuan, Ying Xixiang, Zhang Wenjie, Chen Yinghui, Leng Aijing, Jiang Chen, Liu Jing

机构信息

Regenerative Medicine Center, The First Affiliated Hospital of Dalian Medical University, Dalian, China; Institute of Integrative Medicine, Dalian Medical University, Dalian, China.

出版信息

J Pharm Pharmacol. 2014 Jul;66(7):988-97. doi: 10.1111/jphp.12225. Epub 2014 Feb 17.

DOI:10.1111/jphp.12225
PMID:24533889
Abstract

OBJECTIVES

Vitexin-2"-O-rhamnoside (VOR) and vitexin-4"-O-glucoside (VOG) are the two main flavonoid glycosides of the leaves of Cratagus pinnatifida Bge. var. major N. E. Br. that has been widely used for the treatment of cardiovascular system diseases. In this study, we simultaneously investigated the influence of VOR and VOG on human adipose-derived stem cells (hADSCs) injury induced by hydrogen peroxide (H2 O2 ) to further characterize their anti-oxidative and anti-apoptotic activity.

METHODS

hADSCs were isolated, cultured in vitro and pretreated with 62.5 μm VOR or 120 μm VOG for 24 h and then exposed to 500 μm H2 O2 for an additional 4 h.

KEY FINDINGS

Pretreatment of hADSCs with VOR and VOG was demonstrated to significantly ameliorate the toxicity and apoptosis effects, such as morphological distortion, nuclear condensation, decreased intracellular caspase-3 activity and percentage of cells in apoptosis/necrosis by using morphological assay, immunocytochemistry and flow cytometric evaluation. In addition, VOR and VOG caused no cytotoxic effect on hADSCs at concentrations up to 250 and 480 μm, respectively.

CONCLUSIONS

Our results indicated that both VOR and VOG contribute to the protection against H2 O2 -mediated oxidative stress damage and could be safely used for a wide range of concentrations.

摘要

目的

牡荆素-2″-O-鼠李糖苷(VOR)和牡荆素-4″-O-葡萄糖苷(VOG)是山里红叶片中的两种主要黄酮苷,山里红已被广泛用于治疗心血管系统疾病。在本研究中,我们同时研究了VOR和VOG对过氧化氢(H2O2)诱导的人脂肪来源干细胞(hADSCs)损伤的影响,以进一步表征它们的抗氧化和抗凋亡活性。

方法

分离hADSCs,体外培养,并用62.5μm的VOR或120μm的VOG预处理24小时,然后再用500μm的H2O2处理4小时。

主要发现

通过形态学分析、免疫细胞化学和流式细胞术评估,证明用VOR和VOG预处理hADSCs可显著改善毒性和凋亡效应,如形态扭曲、核浓缩、细胞内caspase-3活性降低以及凋亡/坏死细胞百分比降低。此外,VOR和VOG在分别高达250μm和480μm的浓度下对hADSCs没有细胞毒性作用。

结论

我们的结果表明,VOR和VOG都有助于保护细胞免受H2O2介导的氧化应激损伤,并且在很宽的浓度范围内都可以安全使用。

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