Song Erqun, Xia Xiaomin, Su Chuanyang, Dong Wenjing, Xian Yaping, Wang Wei, Song Yang
Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, People's Republic of China.
Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, People's Republic of China.
Food Chem Toxicol. 2014 Sep;71:122-7. doi: 10.1016/j.fct.2014.06.009. Epub 2014 Jun 17.
Patulin (PAT) is a mycotoxin produced by certain species of Penicillium, Aspergillus, and Byssochlamys. Previous studies demonstrated its cytotoxic, genotoxic, and mutagenic effects in different cell lines. However, there is little information available concerning its toxic behavior in vivo. In the present study, we investigated PAT-induced hepatotoxicity and genotoxicity in mice. We also investigated the antioxidant and anti-genotoxicity efficiency of green tea polyphenols (GTP) against PAT-induced toxicity. We found that PAT-treatment induced serum alanine transaminase (ALT) and aspartate transaminase (AST) activities significantly. PAT-induced lipid peroxidation was confirmed with the elevation of thiobarbituric acid-reactive substances (TBARS). Moreover, the increasing of reactive oxygen species (ROS) and decreasing of GSH level implied its oxidative damage mechanism. In bone marrow cell, PAT was found to induce micronucleus and chromosomal aberration formation. In addition, our result suggested that GTP administration has dose-dependent antioxidative and antigenotoxic effect in against PAT-induced hepatotoxicity and genotoxicity.
展青霉素(PAT)是由某些青霉属、曲霉属和丝衣霉属真菌产生的一种霉菌毒素。先前的研究证明了它在不同细胞系中的细胞毒性、遗传毒性和致突变性。然而,关于其体内毒性行为的信息却很少。在本研究中,我们调查了PAT对小鼠的肝毒性和遗传毒性。我们还研究了绿茶多酚(GTP)对PAT诱导的毒性的抗氧化和抗遗传毒性效果。我们发现,PAT处理显著诱导了血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)的活性。通过硫代巴比妥酸反应性物质(TBARS)的升高证实了PAT诱导的脂质过氧化。此外,活性氧(ROS)的增加和谷胱甘肽(GSH)水平的降低暗示了其氧化损伤机制。在骨髓细胞中,发现PAT可诱导微核和染色体畸变的形成。此外,我们的结果表明,给予GTP对PAT诱导的肝毒性和遗传毒性具有剂量依赖性的抗氧化和抗遗传毒性作用。