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本文引用的文献

1
Nostocyclopeptide-M1: a potent, nontoxic inhibitor of the hepatocyte drug transporters OATP1B3 and OATP1B1.Nostocyclopeptide-M1:一种强效、低毒的肝细胞药物转运体 OATP1B3 和 OATP1B1 的抑制剂。
Mol Pharm. 2011 Apr 4;8(2):360-7. doi: 10.1021/mp1002224. Epub 2011 Jan 24.
2
Activation of Nrf2 by microcystin-LR provides advantages for liver cancer cell growth.微囊藻毒素-LR 通过激活 Nrf2 为肝癌细胞生长提供优势。
Chem Res Toxicol. 2010 Sep 20;23(9):1477-84. doi: 10.1021/tx1001628.
3
Sulforaphane protects Microcystin-LR-induced toxicity through activation of the Nrf2-mediated defensive response.萝卜硫素通过激活 Nrf2 介导的防御反应来保护微囊藻毒素-LR 诱导的毒性。
Toxicol Appl Pharmacol. 2010 Sep 1;247(2):129-37. doi: 10.1016/j.taap.2010.06.005. Epub 2010 Jun 21.
4
Molecular targets of dietary phenethyl isothiocyanate and sulforaphane for cancer chemoprevention.膳食苯乙基异硫氰酸酯和萝卜硫素的癌症化学预防的分子靶点。
AAPS J. 2010 Mar;12(1):87-97. doi: 10.1208/s12248-009-9162-8. Epub 2009 Dec 15.
5
Detection of microcystins in environmental samples using surface plasmon resonance biosensor.利用表面等离子体共振生物传感器检测环境样品中的微囊藻毒素。
Talanta. 2009 Nov 15;80(1):407-10. doi: 10.1016/j.talanta.2009.06.044. Epub 2009 Jun 27.
6
Nrf2 enhances cell proliferation and resistance to anticancer drugs in human lung cancer.Nrf2增强人肺癌细胞的增殖及对抗癌药物的抗性。
Clin Cancer Res. 2009 May 15;15(10):3423-32. doi: 10.1158/1078-0432.CCR-08-2822. Epub 2009 May 5.
7
Time-dependent protective efficacy of Trolox (vitamin E analog) against microcystin-induced toxicity in tilapia (Oreochromis niloticus).Trolox(维生素 E 类似物)对微囊藻毒素诱导的罗非鱼(Oreochromis niloticus)毒性的时间依赖性保护作用。
Environ Toxicol. 2009 Dec;24(6):563-79. doi: 10.1002/tox.20458.
8
Sulforaphane suppressed LPS-induced inflammation in mouse peritoneal macrophages through Nrf2 dependent pathway.萝卜硫素通过Nrf2依赖途径抑制脂多糖诱导的小鼠腹腔巨噬细胞炎症。
Biochem Pharmacol. 2008 Oct 15;76(8):967-73. doi: 10.1016/j.bcp.2008.07.036. Epub 2008 Aug 7.
9
Nrf2 signaling: an adaptive response pathway for protection against environmental toxic insults.Nrf2信号传导:一种针对环境毒性损伤的适应性保护反应途径。
Mutat Res. 2008 Jul-Aug;659(1-2):31-9. doi: 10.1016/j.mrrev.2007.11.006. Epub 2007 Nov 23.
10
Involvement of reactive oxygen species in Microcystin-LR-induced cytogenotoxicity.活性氧在微囊藻毒素-LR诱导的细胞遗传毒性中的作用。
Free Radic Res. 2007 Dec;41(12):1326-37. doi: 10.1080/10715760701704599.

萝卜硫素可预防微囊藻毒素-LR 诱导的 BALB/c 小鼠氧化损伤和细胞凋亡。

Sulforaphane prevents microcystin-LR-induced oxidative damage and apoptosis in BALB/c mice.

机构信息

State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, CAS, People's Republic of China.

出版信息

Toxicol Appl Pharmacol. 2011 Aug 15;255(1):9-17. doi: 10.1016/j.taap.2011.05.011. Epub 2011 May 27.

DOI:10.1016/j.taap.2011.05.011
PMID:21684301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3577421/
Abstract

Microcystins (MCs), the products of blooming algae Microcystis, are waterborne environmental toxins that have been implicated in the development of liver cancer, necrosis, and even fatal intrahepatic bleeding. Alternative protective approaches in addition to complete removal of MCs in drinking water are urgently needed. In our previous work, we found that sulforaphane (SFN) protects against microcystin-LR (MC-LR)-induced cytotoxicity by activating the NF-E2-related factor 2 (Nrf2)-mediated defensive response in human hepatoma (HepG2) and NIH 3T3 cells. The purpose of this study was to investigate and confirm efficacy the SFN-induced multi-mechanistic defense system against MC-induced hepatotoxicity in an animal model. We report that SFN protected against MC-LR-induced liver damage and animal death at a nontoxic and physiologically relevant dose in BALB/c mice. The protection by SFN included activities of anti-cytochrome P450 induction, anti-oxidation, anti-inflammation, and anti-apoptosis. Our results suggest that SFN may protect mice against MC-induced hepatotoxicity. This raises the possibility of a similar protective effect in human populations, particularly in developing countries where freshwaters are polluted by blooming algae.

摘要

微囊藻毒素(MCs)是藻类水华产生的产物,是一种水生环境毒素,与肝癌的发展、坏死,甚至致命的肝内出血有关。除了在饮用水中完全去除 MCs 之外,还迫切需要其他替代的保护方法。在我们之前的工作中,我们发现萝卜硫素(SFN)通过激活 NF-E2 相关因子 2(Nrf2)介导的防御反应,在人肝癌(HepG2)和 NIH 3T3 细胞中保护免受微囊藻毒素-LR(MC-LR)诱导的细胞毒性。本研究旨在研究和确认 SFN 诱导的多机制防御系统对 MC 诱导的动物模型肝毒性的疗效。我们报告 SFN 在 BALB/c 小鼠中以非毒性和生理相关剂量保护免受 MC-LR 诱导的肝损伤和动物死亡。SFN 的保护作用包括细胞色素 P450 诱导、抗氧化、抗炎和抗凋亡活性。我们的结果表明,SFN 可能保护小鼠免受 MC 诱导的肝毒性。这提出了在人类中可能具有类似保护作用的可能性,特别是在受藻类水华污染的淡水的发展中国家。