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香烟焦油提取物的分级分离:含有焦油自由基的级分可导致DNA损伤。

Fractionation of aqueous cigarette tar extracts: fractions that contain the tar radical cause DNA damage.

作者信息

Pryor W A, Stone K, Zang L Y, Bermúdez E

机构信息

Biodynamics Institute, 711 Choppin Hall, Louisiana State University, Baton Rouge, Louisiana 70803-1800, USA.

出版信息

Chem Res Toxicol. 1998 May;11(5):441-8. doi: 10.1021/tx970159y.

Abstract

Previously, we have shown that aqueous cigarette tar (ACT) extracts contain a long-lived tar radical that associates with DNA in isolated rat alveolar macrophages and causes DNA damage in isolated rat thymocytes. These ACT solutions reduce oxygen to produce superoxide and, ultimately, hydrogen peroxide. In this study, we report the fractionation of ACT solutions prepared from the tar from five cigarettes using Sephadex columns. The fractions were analyzed by UV and electron paramagnetic resonance (EPR) spectroscopy and gas chromatography/mass spectrometry (GC/MS). The fractions containing polyphenolic species (principally catechol and hydroquinone, as determined by MS) caused most of the observed DNA damage in rat thymocytes. These DNA-damaging fractions produced superoxide, H2O2, and hydroxyl radicals. Stable free radicals were identified as o- and p-benzosemiquinone radicals by EPR spectroscopy. Hydroxyl radicals were detected by EPR spin-trapping with 5, 5-dimethyl-1-pyrroline N-oxide (DMPO). Catalase inhibited the EPR signal of the DMPO-OH adduct, indicating that H2O2 is the precursor of the hydroxyl radical spin adduct. The Sephadex separation resulted in a 90-fold concentration of the hydrogen peroxide-generating capacity of the fractions that contained polyphenols, relative to the unfractionated ACT solution. Another fraction, which contained nicotine, caused some DNA damage, but this damage was 28-fold less than the damage caused by the most damaging phenolic fraction. These results support our hypothesis that the tar radical system is an equilibrium mixture of semiquinones, hydroquinones, and quinones. The tar radical associates with DNA, causes DNA damage, and very likely is involved in the toxicity associated with cigarette smoking.

摘要

此前,我们已经表明,香烟焦油水溶液(ACT)提取物含有一种长寿命的焦油自由基,该自由基可与分离出的大鼠肺泡巨噬细胞中的DNA结合,并导致分离出的大鼠胸腺细胞中的DNA损伤。这些ACT溶液可将氧气还原以产生超氧化物,并最终生成过氧化氢。在本研究中,我们报告了使用葡聚糖凝胶柱对由五支香烟的焦油制备的ACT溶液进行分级分离的情况。通过紫外光谱、电子顺磁共振(EPR)光谱和气相色谱/质谱联用(GC/MS)对各馏分进行了分析。含有多酚类物质的馏分(通过质谱测定主要为邻苯二酚和对苯二酚)在大鼠胸腺细胞中造成了大部分观察到的DNA损伤。这些具有DNA损伤作用的馏分会产生超氧化物、过氧化氢和羟基自由基。通过EPR光谱鉴定出稳定自由基为邻苯并半醌自由基和对苯并半醌自由基。通过用5,5-二甲基-1-吡咯啉N-氧化物(DMPO)进行EPR自旋捕获检测到了羟基自由基。过氧化氢酶抑制了DMPO-OH加合物的EPR信号,表明过氧化氢是羟基自由基自旋加合物的前体。相对于未分级的ACT溶液,葡聚糖凝胶分离使含有多酚的馏分产生过氧化氢的能力提高了90倍。另一个含有尼古丁的馏分造成了一些DNA损伤,但这种损伤比最具损伤性的酚类馏分造成的损伤小28倍。这些结果支持了我们的假设,即焦油自由基系统是半醌、对苯二酚和醌的平衡混合物。焦油自由基与DNA结合,导致DNA损伤,并且很可能参与了与吸烟相关的毒性作用。

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