二十二碳六烯酸抑制葡萄糖变异性诱导的血管平滑肌细胞增殖。

The Open Biochemistry Journal Pub Date : 2017-06-30 eCollection Date: 2017-01-01 DOI:10.2174/1874091X01711010056
Kaliyaperumal Rani, Nway Y Aung
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引用次数: 11

摘要

背景:血管平滑肌细胞(VSMC)在早期血管形成和维持血管完整性中起着至关重要的作用。然而,VSMC的异常增殖并迁移到血管壁导致血管病变的形成,导致血管基底膜的变性和重塑。在糖尿病中,高血糖加速VSMC增殖,并有助于动脉粥样硬化病变的发生和进展。近年来,急性血糖波动与VSMC异常增殖和糖尿病动脉粥样硬化并发症有关。二十二碳六烯酸(DHA)是一种ω-3多不饱和脂肪酸(PUFA),已被证明可以抑制几种细胞类型的增殖,涉及几种不同的机制。在本研究中,我们研究了DHA对稳定和间歇性高糖诱导的VSMC增殖的影响。方法:用DHA处理大鼠主动脉VSMCs融合培养24 h,然后稳定高糖(25 mmol/L, SHG)或间歇性高糖(5 mmol/L和25 mmol/L每12 h交替,IHG) 72 h。MTT法检测细胞增殖,Hoechst染色法、流式细胞术和caspase-3活性法检测细胞凋亡过程。结果:我们的数据表明,DHA预处理显著抑制了稳定和间歇性高糖诱导的超增殖。DHA显著增加caspase-3活性,导致DNA断裂和细胞凋亡增加。结论:DHA可降低高糖诱导的VSMC增殖,诱导细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Docosahexaenoic Acid Inhibits Vascular Smooth Muscle Cell Proliferation Induced by Glucose Variability.

Docosahexaenoic Acid Inhibits Vascular Smooth Muscle Cell Proliferation Induced by Glucose Variability.

Docosahexaenoic Acid Inhibits Vascular Smooth Muscle Cell Proliferation Induced by Glucose Variability.

Docosahexaenoic Acid Inhibits Vascular Smooth Muscle Cell Proliferation Induced by Glucose Variability.

Background: Vascular Smooth Muscle cells (VSMC) enact crucial roles in early vasculogenesis and sustenance of vascular integrity. However, aberrant proliferation of VSMC followed by migration into the blood vessel wall leads to the formation of vascular lesions accounting for the degeneration and remodelling of vascular basement membrane. In diabetes, hyperglycaemia accelerates VSMC proliferation and contributes to the initiation and progression of atherosclerotic lesions. Recently, acute glucose fluctuations have been implicated in the abnormal VSMC proliferation and complications of diabetic atherosclerosis. Docosahexaenoic acid (DHA), a ω-3 polyunsaturated fatty acid (PUFA) has been shown to inhibit proliferation of several cell types implicating several different mechanisms. In the present study, we have investigated the effects of DHA on VSMC proliferation induced by stable and intermittent high glucose levels.

Method: Confluent cultures of rat aortic VSMCs were treated with DHA for 24 hrs and then exposed to stable high glucose (25 mmol/L, SHG) or intermittent high glucose (5 mmol/L and 25 mmol/L alternating every 12 hrs, IHG) for 72 hrs. Cell proliferation was examined by the MTT viability assay, while apoptosis process was evaluated by the Hoechst staining, flow cytometry and caspase-3 activity assays.

Results: Our data demonstrated that the hyper proliferation induced by stable and intermittent high glucose levels was significantly inhibited by the DHA pre-treatment. DHA significantly increased caspase-3 activity, resulting in enhanced DNA fragmentation and apoptosis.

Conclusion: Our results suggest that DHA reduced the high glucose-induced proliferation of VSMC and induced cell apoptosis.

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