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汉黄芩素通过减少内源性半胱天冬酶途径的激活,减轻了双酚A缩水甘油醚在巨噬细胞中诱导的细胞毒性和基因毒性。

BisGMA-induced cytotoxicity and genotoxicity in macrophages are attenuated by wogonin via reduction of intrinsic caspase pathway activation.

作者信息

Huang Fu-Mei, Chang Yu-Chao, Lee Shiuan-Shinn, Yeh Chung-Hsin, Lee Kevin Gee, Huang Yi-Chun, Chen Chun-Jung, Chen Wen-Ying, Pan Pin-Ho, Kuan Yu-Hsiang

机构信息

School of Dentistry, Chung Shan Medical University, Taichung, Taiwan.

School of Public Health, Chung Shan Medical University, Taichung, Taiwan.

出版信息

Environ Toxicol. 2016 Feb;31(2):176-84. doi: 10.1002/tox.22032. Epub 2014 Aug 1.

Abstract

Bisphenol-A-glycidyldimethacrylate (BisGMA) is a frequently used monomer in dental restorative resins. However, BisGMA could leach from dental restorative resins after polymerization leading to inflammation in the peripheral environment. Wogonin, a natural flavone derivative, has several benefits, such as antioxidative, anti-inflammatory and neuroprotective properties. Pretreatment of macrophage RAW264.7 cells with wogonin inhibited cytotoxicity which is induced by BisGMA in a concentration-dependent manner. BisGMA induced apoptotic responses, such as redistribution of phosphatidylserine from the internal to the external membrane and DNA fragmentation, were decreased by wogonin in a concentration-dependent manner. In addition, BisGMA-induced genotoxicity, which detected by cytokinesis-blocked micronucleus and single-cell gel electrophoresis assays, were inhibited by wogonin in a concentration-dependent manner. Furthermore, wogonin suppressed BisGMA-induced activation of intrinsic caspase pathways, such as caspases-3 and -8. Parallel trends were observed in inhibition of caspase-3 and -8 activities, apoptosis, and genotoxicity. These results indicate wogonin suppressed the BisGMA-induced apoptosis and genotoxicity mainly via intrinsic caspase pathway in macrophages.

摘要

双酚A-缩水甘油二甲基丙烯酸酯(BisGMA)是牙科修复树脂中常用的单体。然而,BisGMA在聚合后可能会从牙科修复树脂中渗出,导致周围环境发生炎症。汉黄芩素是一种天然黄酮衍生物,具有多种益处,如抗氧化、抗炎和神经保护特性。用汉黄芩素预处理巨噬细胞RAW264.7细胞可抑制由BisGMA诱导的细胞毒性,且呈浓度依赖性。BisGMA诱导的凋亡反应,如磷脂酰丝氨酸从内膜重新分布到外膜以及DNA片段化,均被汉黄芩素以浓度依赖性方式降低。此外,通过胞质分裂阻滞微核试验和单细胞凝胶电泳试验检测到的BisGMA诱导的遗传毒性,也被汉黄芩素以浓度依赖性方式抑制。此外,汉黄芩素抑制了BisGMA诱导的内源性半胱天冬酶途径的激活,如半胱天冬酶-3和-8。在抑制半胱天冬酶-3和-8活性、凋亡和遗传毒性方面观察到了平行趋势。这些结果表明,汉黄芩素主要通过巨噬细胞中的内源性半胱天冬酶途径抑制了BisGMA诱导的凋亡和遗传毒性。

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