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硬脂酸接枝壳寡糖纳米胶束的遗传毒性评价。

Genotoxicity evaluation of stearic acid grafted chitosan oligosaccharide nanomicelles.

机构信息

Department of Toxicology, Zhejiang University School of Public Health, Hangzhou, Zhejiang, China.

出版信息

Mutat Res. 2013 Mar 18;751(2):116-26. doi: 10.1016/j.mrgentox.2012.12.004. Epub 2012 Dec 27.

Abstract

Stearic acid grafted chitosan oligosaccharide (CSO-SA) nanomicelles could be promptly internalized into cancer cells; therefore, it is regarded as a promising drug carrier for cancer therapy. However, the toxicity of CSO-SA is not clear. In the present study, the genotoxic effects of CSO-SA nanomicelles (with high substitution degree of SA, 42.6±3.8%) were evaluated with a battery of genotoxicity assays. Mutagenicity was not found in Ames Salmonella/microsome mutagenicity assay (Ames test), while mild but definite positive results were observed in mouse bone marrow micronucleus assay and single cell gel electrophoresis (SCGE or comet assay) in A549 cells. CSO-SA was also found to induce apoptosis and oxidative stress through the induction of reactive oxygen species (ROS) in a dose-dependent manner in A549 cells. Preincubation with the free radical scavenger N-acetyl-l-cysteine (NAC) decreased the intracellular ROS level and alleviated the DNA damage in A549 cells. Expression levels of cleaved poly ADP-ribose polymerase (PARP), caspase-9 and caspase-3, markers of apoptosis, were significantly higher in CSO-SA treated cells. In conclusion, these results suggested significant genotoxicity of high doses of CSO-SA nanomicelles in vivo and in vitro. Oxidative stress was, at least partially, the possible mechanism underlying the genotoxicity induced by CSO-SA.

摘要

硬脂酸接枝壳聚糖寡糖(CSO-SA)纳米胶束可以迅速被癌细胞内化;因此,它被认为是一种很有前途的癌症治疗药物载体。然而,CSO-SA 的毒性尚不清楚。在本研究中,采用一系列遗传毒性试验评价了 CSO-SA 纳米胶束(SA 高取代度,42.6±3.8%)的遗传毒性。在 Ames 沙门氏菌/微粒体致突变试验(Ames 试验)中未发现致突变性,而在小鼠骨髓微核试验和 A549 细胞单细胞凝胶电泳(SCGE 或彗星试验)中观察到轻度但明确的阳性结果。CSO-SA 还通过诱导 A549 细胞中活性氧(ROS)的产生,以剂量依赖的方式诱导细胞凋亡和氧化应激。在 A549 细胞中,用自由基清除剂 N-乙酰-L-半胱氨酸(NAC)预处理可降低细胞内 ROS 水平并减轻 DNA 损伤。CSO-SA 处理的细胞中,细胞凋亡标志物 cleaved poly ADP-ribose polymerase(PARP)、caspase-9 和 caspase-3 的表达水平显著升高。总之,这些结果表明 CSO-SA 纳米胶束在体内和体外具有显著的遗传毒性。氧化应激至少部分是 CSO-SA 诱导遗传毒性的可能机制。

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