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口服呋喃对小鼠肝脏的毒性和遗传毒性作用。

Toxic and genotoxic effects of oral administration of furan in mouse liver.

机构信息

Section of Toxicology and Biomedical Sciences, ENEA CR Casaccia, Research Center Casaccia, Via Anguillarese 301, 00123-Rome, Italy.

出版信息

Mutagenesis. 2010 May;25(3):305-14. doi: 10.1093/mutage/geq007. Epub 2010 Mar 1.

Abstract

In this study, the effects induced in mouse liver by repeated oral exposure to furan were investigated. To this aim, the compound was given for 28 days by daily gavage to male B6C3F1 mice at 2, 4, 8 and 15 mg/kg body weight (b.w.)/day. Twenty-four hours after last administration, animals were sacrificed, liver was excised and the following parameters were evaluated: histological alterations, apoptosis, cell proliferation, polyploidy, overall DNA methylation, gene expression and DNA damage by the immunofluorescence detection of foci of phosphorylated histone H2AX (gamma-H2AX) and by alkaline comet assays, using both standard and modified protocols for the detection of DNA cross links. Liver DNA damage by comet assays was also evaluated in mice receiving furan as a single acute oral dose (15, 100 or 250 mg/kg b.w.). Microscopic analysis of liver sections indicated that repeated oral administration of furan was moderately toxic, producing mild histological alterations with necrotic figures, apoptosis and limited regenerative cell proliferation. The flow cytometric analysis of DNA content in single-cell suspensions of liver cells showed a statistically significant increase in polyploid (8N) cells at the highest dose. No treatment-related changes in overall DNA methylation, gamma-H2AX foci, DNA strand breaks and cross links were observed at the end of the 4-week exposure period. However, several genes involved in DNA damage response, beyond stress and liver toxicity, were over-expressed in mice treated with the highest furan dose (15 mg/kg b.w./day). Acute administration of furan induced evident liver toxicity at the highest dose (250 mg/kg b.w.), which was associated with a significant increase of DNA damage in the alkaline comet assay and with a distinct decrease in gamma-ray-induced DNA migration. Overall, the results obtained suggest that the contribution of genotoxicity to the mechanism of furan carcinogenicity in mouse liver should not be dismissed.

摘要

本研究旨在探讨反复经口给予呋喃对小鼠肝脏的影响。为此,雄性 B6C3F1 小鼠每日经口灌胃给予呋喃 28 天,剂量分别为 2、4、8 和 15mg/kg 体重/天。末次给药 24 小时后处死动物,取肝脏,评估以下参数:组织学改变、细胞凋亡、细胞增殖、多倍体形成、总体 DNA 甲基化、基因表达和 DNA 损伤,通过免疫荧光检测磷酸化组蛋白 H2AX(γ-H2AX)焦点和碱性彗星试验进行检测,分别使用标准和改良的检测 DNA 交联的方案。还通过彗星试验评估了单次急性经口给予呋喃(15、100 或 250mg/kg 体重)后小鼠肝脏的 DNA 损伤。肝脏切片的显微镜分析表明,反复经口给予呋喃具有中度毒性,导致轻微的组织学改变,伴有坏死、凋亡和有限的再生细胞增殖。单细胞悬液中肝细胞核 DNA 含量的流式细胞分析显示,在最高剂量下多倍体(8N)细胞的数量有统计学意义的增加。在 4 周暴露期结束时,未观察到总 DNA 甲基化、γ-H2AX 焦点、DNA 链断裂和交联与处理相关的变化。然而,在最高呋喃剂量(15mg/kg 体重/天)处理的小鼠中,多个参与 DNA 损伤反应的基因(除应激和肝毒性外)表达过度。急性给予呋喃在最高剂量(250mg/kg 体重)下引起明显的肝毒性,与碱性彗星试验中 DNA 损伤的显著增加以及 γ 射线诱导的 DNA 迁移明显减少相关。总体而言,研究结果表明,遗传毒性不应被排除在呋喃在小鼠肝脏致癌机制中的作用之外。

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