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多壁碳纳米管在小鼠体内的肝毒性。

The hepatotoxicity of multi-walled carbon nanotubes in mice.

机构信息

Department of Gastroenterology, Zhongshan Hospital, Shanghai Medical College, Fudan University, Shanghai 200032, People's Republic of China.

出版信息

Nanotechnology. 2009 Nov 4;20(44):445101. doi: 10.1088/0957-4484/20/44/445101. Epub 2009 Oct 5.

DOI:10.1088/0957-4484/20/44/445101
PMID:19801780
Abstract

The hepatotoxicity of two types of multi-walled carbon nanotubes (MWCNTs), acid-oxidized MWCNTs (O-MWCNTs) and Tween-80-dispersed MWCNTs (T-MWCNTs), were investigated with Kunming mice exposed to 10 and 60 mg kg(-1) by intravenous injection for 15 and 60 d. Compared with the PBS group, the body-weight gain of the mice decreased and the level of total bilirubin and aspartate aminotransferase increased in the MWCNT-exposed group with a significant dose-effect relationship, while tumor necrosis factor alpha level did not show significant statistical change within 60 d. Spotty necrosis, inflammatory cell infiltration in portal region, hepatocyte mitochondria swelling and lysis were observed with a significant dose-effect relationship in the MWCNT groups. Liver damage of the T-MWCNT group was more severe than that of the O-MWCNT group according to the Roenigk classification system. Furthermore, T-MWCNTs induce slight liver oxidative damage in mice at 15 d, which was recovered at 60 d. Part of the gene expressions of mouse liver in the MWCNT groups changed compared to the PBS group, including GPCRs (G protein-coupled receptors), cholesterol biosynthesis, metabolism by cytochrome P450, natural-killer-cell-mediated cytotoxicity, TNF- alpha, NF-kappaB signaling pathway, etc. In the P450 pathway, the gene expressions of Gsta2 (down-regulated), Cyp2B19 (up-regulated) and Cyp2C50 (down-regulated) had significant changes in the MWCNT groups. These results show that a high dose of T-MWCNTs can induce hepatic toxicity in mice while O-MWCNTs seem to have less toxicity.

摘要

两种类型的多壁碳纳米管(MWCNTs),酸氧化 MWCNTs(O-MWCNTs)和 Tween-80 分散的 MWCNTs(T-MWCNTs)的肝毒性,用昆明小鼠进行了研究,通过静脉注射暴露于 10 和 60 mg kg(-1) 15 和 60 d。与 PBS 组相比,MWCNT 暴露组的体重增加减少,总胆红素和天冬氨酸转氨酶水平升高,呈明显的剂量-效应关系,而肿瘤坏死因子-α水平在 60 d 内无显著统计学变化。MWCNT 组出现点状坏死、门脉区炎性细胞浸润、肝细胞线粒体肿胀和溶解,呈明显的剂量-效应关系。根据 Roenigk 分类系统,T-MWCNT 组的肝损伤比 O-MWCNT 组更严重。此外,T-MWCNTs 在 15 d 时引起小鼠轻微的肝氧化损伤,在 60 d 时恢复。与 PBS 组相比,MWCNT 组小鼠肝脏的部分基因表达发生了变化,包括 GPCRs(G 蛋白偶联受体)、胆固醇生物合成、细胞色素 P450 代谢、自然杀伤细胞介导的细胞毒性、TNF-α、NF-κB 信号通路等。在 P450 通路中,Gsta2(下调)、Cyp2B19(上调)和 Cyp2C50(下调)的基因表达在 MWCNT 组中发生了显著变化。这些结果表明,高剂量的 T-MWCNTs 可诱导小鼠肝毒性,而 O-MWCNTs 似乎毒性较小。

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