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4,4'-亚甲基二苯胺诱导的急性肝毒性中的基因表达分析

Analysis of Gene Expression in 4,4'-Methylenedianiline-induced Acute Hepatotoxicity.

作者信息

Oh Jung-Hwa, Yoon Hea-Jin, Lim Jung-Sun, Park Han-Jin, Cho Jae-Woo, Kwon Myung-Sang, Yoon Seokjoo

机构信息

14Toxicogenomics Team, Korea Institute of Toxicology, 19 Shinsung-ro, Yuseoung, Daejeon, 305-343 Korea.

24Clinical Pathology Team, Korea Institute of Toxicology, 19 Shinsung-ro, Yuseoung, Daejeon, 305-343 Korea.

出版信息

Toxicol Res. 2009 Jun;25(2):85-92. doi: 10.5487/TR.2009.25.2.085. Epub 2009 Jun 1.

Abstract

4,4'-Methylenedianiline (MDA) is an aromatic amine that is widely used in the industrial synthetic process. Genotoxic MDA forms DNA adducts in the liver and is known to induce liver damage in human and rats. To elucidate the molecular mechanisms associated with MDA-induced hepatotoxicity, we have identified genes differentially expressed by microarray approach. BALB/c male mice were treated once daily with MDA (20 mg/kg) up to 7 days via intraperitoneal injection (i.p.) and hepatic damages were revealed by histopathological observation and elevation of serum marker enzymes such as AST, ALT, ALP, cholesterol, DBIL, and TBIL. Microarray analysis showed that 952 genes were differentially expressed in the liver of MDA-treated mice and their biological functions and canonical pathways were further analyzed using Ingenuity Pathways Analysis (IPA). Toxicological functional analysis showed that genes related to hepatotoxicity such hyperplasia/hyperproliferation (), necrosis/cell death (, and ), hemorrhaging (), cholestasis (, and ), and inflammation ( and ) were differentially expressed in MDA-treated group. This gene expression profiling should be useful for elucidating the genetic events associated with aromatic amine-induced hepatotoxicity and for discovering the potential biomarkers for hepatotoxicity.

摘要

4,4'-亚甲基二苯胺(MDA)是一种芳香胺,在工业合成过程中被广泛使用。具有基因毒性的MDA在肝脏中形成DNA加合物,已知会在人和大鼠中诱发肝损伤。为了阐明与MDA诱导的肝毒性相关的分子机制,我们通过微阵列方法鉴定了差异表达的基因。通过腹腔注射(i.p.),每天给BALB/c雄性小鼠注射一次MDA(20 mg/kg),持续7天,通过组织病理学观察以及血清标志物酶如AST、ALT、ALP、胆固醇、直接胆红素和总胆红素的升高来揭示肝损伤。微阵列分析表明,952个基因在MDA处理的小鼠肝脏中差异表达,并使用Ingenuity Pathways Analysis(IPA)进一步分析了它们的生物学功能和典型通路。毒理学功能分析表明,与肝毒性相关的基因,如增生/过度增殖()、坏死/细胞死亡(和)、出血()、胆汁淤积(和)以及炎症(和)在MDA处理组中差异表达。这种基因表达谱分析对于阐明与芳香胺诱导的肝毒性相关的遗传事件以及发现肝毒性的潜在生物标志物应该是有用的。

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