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镉通过芳香胺 N-乙酰基转移酶外源性代谢酶改变致癌芳香胺的生物转化:分子、细胞和体内研究。

Cadmium alters the biotransformation of carcinogenic aromatic amines by arylamine N-acetyltransferase xenobiotic-metabolizing enzymes: molecular, cellular, and in vivo studies.

机构信息

Université Paris Diderot-Paris 7, Unité de Biologie Fonctionnelle et Adaptative, Centre National de la Recherche Scientifique, Paris, France.

出版信息

Environ Health Perspect. 2010 Dec;118(12):1685-91. doi: 10.1289/ehp.1002334. Epub 2010 Sep 1.

Abstract

BACKGROUND

Cadmium (Cd) is a carcinogenic heavy metal of environmental concern. Exposure to both Cd and carcinogenic organic compounds, such as polycyclic aromatic hydrocarbons or aromatic amines (AAs), is a common environmental problem. Human arylamine N-acetyltransferases (NATs) are xenobiotic-metabolizing enzymes that play a key role in the biotransformation of AA carcinogens. Changes in NAT activity have long been associated with variations in susceptibility to different cancers in relation with exposure to certain AAs.

OBJECTIVE

We explored the possible interactions between Cd and the NAT-dependent biotransformation of carcinogenic AAs.

METHODS

We exposed purified enzymes, lung epithelial cells, and mouse models to Cd and subsequently analyzed NAT-dependent metabolism of AAs.

RESULTS

We found that Cd, at biologically relevant concentrations, impairs the NAT-dependent acetylation of carcinogenic AAs such as 2-aminofluorene (2-AF) in lung epithelial cells. NAT activity was strongly impaired in the tissues of mice exposed to Cd. Accordingly, mice exposed to Cd and 2-AF displayed altered in vivo toxicokinetics with a significant decrease (~ 50%) in acetylated 2-AF in plasma. We found that human NAT1 was rapidly and irreversibly inhibited by Cd [median inhibitory concentration (IC₅₀) ≈ 55 nM; rate inhibition constant (k(inact)) = 5 × 10⁴ M⁻¹ • sec⁻¹], with results of acetyl coenzyme A (acetyl-CoA) protection assays indicating that Cd-mediated inhibition was due to the reaction of metal with the active-site cysteine residue of the enzyme. We found similar results for human NAT2, although this isoform was less sensitive to inactivation (IC₅₀ ≈ 1 μM; k(inact) = 1 × 10⁴ M⁻¹ • sec⁻¹).

CONCLUSIONS

Our data suggest that Cd can alter the metabolism of carcinogenic AAs through the impairment of the NAT-dependent pathway, which may have important toxicological consequences.

摘要

背景

镉(Cd)是一种环境关注的致癌重金属。接触镉和致癌有机化合物,如多环芳烃或芳香胺(AAs),是一个常见的环境问题。人类芳香胺 N-乙酰基转移酶(NATs)是一种外源性代谢酶,在芳香胺致癌物的生物转化中起着关键作用。NAT 活性的变化长期以来与接触某些 AAs 时对不同癌症的易感性变化有关。

目的

我们探讨了 Cd 与致癌芳香胺的 NAT 依赖性生物转化之间可能存在的相互作用。

方法

我们将纯化的酶、肺上皮细胞和小鼠模型暴露于 Cd 下,然后分析 NAT 依赖性芳香胺代谢。

结果

我们发现,在生物学相关浓度下,Cd 会损害肺上皮细胞中致癌芳香胺如 2-氨基芴(2-AF)的 NAT 依赖性乙酰化。暴露于 Cd 的小鼠组织中的 NAT 活性受到强烈抑制。因此,暴露于 Cd 和 2-AF 的小鼠显示出改变的体内毒代动力学,血浆中乙酰化 2-AF 显著减少(约 50%)。我们发现人 NAT1 被 Cd 快速且不可逆地抑制[中值抑制浓度(IC₅₀)≈55 nM;速率抑制常数(k(inact))=5×10⁴ M⁻¹ • sec⁻¹],乙酰辅酶 A(acetyl-CoA)保护实验的结果表明,Cd 介导的抑制是由于金属与酶的活性部位半胱氨酸残基的反应。我们对人 NAT2 也得到了类似的结果,尽管该同工酶对失活的敏感性较低(IC₅₀≈1 μM;k(inact)=1×10⁴ M⁻¹ • sec⁻¹)。

结论

我们的数据表明,Cd 可以通过损害 NAT 依赖性途径来改变致癌芳香胺的代谢,这可能具有重要的毒理学后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf6/3002187/df6508448e5f/ehp-118-1685f1.jpg

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