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CYP450 介导线粒体 ROS 产生参与了槟榔碱 N-氧化物诱导的肝细胞系氧化损伤。

CYP450-mediated mitochondrial ROS production involved in arecoline N-oxide-induced oxidative damage in liver cell lines.

机构信息

Department of Biomedical Sciences, Chung Shan Medical University, Taichung, Taiwan.

Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.

出版信息

Environ Toxicol. 2018 Oct;33(10):1029-1038. doi: 10.1002/tox.22588. Epub 2018 Jul 2.

Abstract

BACKGROUND

IARC has classified the betel nut as a human environmental carcinogen. Previous studies have found that arecoline (AR) is the major alkaloid present in the saliva of betel quid chewers. Saliva contains a large content of AR which has been further shown to cause mutation of oral mucosa cells, resulting in oral cancer. Whereas, to date, there are only few studies reported the hepatotoxicity associated with arecoline and betel nut chewing. Therefore, the main purpose of this study was to determine the toxic effects of AR and its oxidative metabolite, arecoline N-oxide (ARNO), in normal liver cell lines.

METHODS

The cytotoxic, genotoxic, and mutagenic effects were detected by crystal violet staining, alkaline comet assay, and Salmonella mutagenicity test, respectively. Measurement of intracellular reactive oxygen species (ROS) generation was determined using the H2-DCFDA assay.

RESULTS

Our results demonstrated that ARNO exerted higher cytotoxicity, DNA damage, and mutagenicity than its parent compound arecoline in liver cells. Antioxidants, such as N-acetylcysteine, Trolox, and penicillamine, strongly protected liver cells from ARNO-induced DNA damage and ROS production. Furthermore, co-treatment with Mito-TEMPO also effectively blocked ARNO-induced ROS production in liver cells. Besides antioxidants, co-treatment with 1-aminobenzotriazole and methimazole nearly completely suppressed ARNO-induced ROS production in liver cells.

CONCLUSIONS

Our data suggest that arecoline ingested from the habit of chewing betel quid can be primarily oxidized to ARNO, thereby enhancing its toxicity through increased ROS production. Considering the excellent protective effects of both mitochondria-targeted antioxidant and CYP450 inhibitor on ARNO-induced ROS production in liver cells, mitochondria CYP450-mediated metabolism of ARNO may be a key mechanism. Collectively, our results provide novel cellular evidence for the positive connection between habitual betel quid chewing and the risk for liver damage.

摘要

背景

国际癌症研究机构已将槟榔果列为人类环境致癌物。先前的研究发现,槟榔碱(AR)是咀嚼槟榔者唾液中的主要生物碱。唾液中含有大量的 AR,进一步研究表明,它会导致口腔黏膜细胞发生突变,从而引发口腔癌。然而,迄今为止,仅有少数研究报道了与食用槟榔和咀嚼槟榔相关的肝毒性。因此,本研究的主要目的是确定 AR 及其氧化代谢物槟榔碱 N-氧化物(ARNO)在正常肝细胞系中的毒性作用。

方法

通过结晶紫染色、碱性彗星试验和沙门氏菌致突变试验分别检测细胞毒性、遗传毒性和致突变性。通过 H2-DCFDA 测定法测定细胞内活性氧(ROS)的产生。

结果

我们的结果表明,ARNO 在肝细胞中的细胞毒性、DNA 损伤和致突变性均高于其母体化合物槟榔碱。抗氧化剂,如 N-乙酰半胱氨酸、Trolox 和青霉胺,可强烈保护肝细胞免受 ARNO 诱导的 DNA 损伤和 ROS 产生。此外,Mito-TEMPO 共处理也能有效地阻断 ARNO 诱导的肝细胞内 ROS 产生。除了抗氧化剂外,1-氨基苯并三唑和甲巯咪唑的共处理几乎完全抑制了 ARNO 诱导的肝细胞内 ROS 产生。

结论

我们的数据表明,咀嚼槟榔习惯摄入的槟榔碱可主要被氧化为 ARNO,从而通过增加 ROS 产生增强其毒性。考虑到线粒体靶向抗氧化剂和 CYP450 抑制剂对 ARNO 诱导的肝细胞内 ROS 产生的优异保护作用,ARNO 的 CYP450 介导的代谢可能是一个关键机制。总之,我们的研究结果为习惯性咀嚼槟榔与肝损伤风险之间的正相关关系提供了新的细胞证据。

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