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自动化分析 TCDF 在 C57BL/6 小鼠中相对肝基因表达效力的剂量反应。

Automated dose-response analysis of the relative hepatic gene expression potency of TCDF in C57BL/6 mice.

机构信息

Department of Biochemistry & Molecular Biology, Michigan State University, 501 Biochemistry Building, Wilson Road, East Lansing, MI 48824-1319, USA.

出版信息

Toxicol Sci. 2009 Nov;112(1):221-8. doi: 10.1093/toxsci/kfp180. Epub 2009 Aug 12.

Abstract

Toxic equivalency factors (TEFs) are assigned to dioxin-like chemicals based on relative potency (REP) values of individual adaptive and toxic responses compared to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Agilent 4x44K oligonucleotide microarrays were used to examine the hepatic gene expression potency of 2,3,7,8-tetrachlorodibenzofuran (TCDF), relative to TCDD with complementary histopathology, TCDD and TCDF tissue level analysis, and ethoxyresorufin-O-deethylase (EROD) assay data. Immature ovariectomized C57BL/6 mice were gavaged with 0.03, 0.1, 0.3, 1, 3, 10, 30, or 100 microg/kg TCDD, the World Health Organization TEF-adjusted doses (10 x TCDD dose) of TCDF (0.3, 1, 3, 10, 30, 100, or 300 microg/kg), or sesame oil vehicle and killed at 72 h. Two thousand two hundred eighty-eight and 1347 genes were differentially expressed (P1(t) > 0.90) at one or more doses by TCDD and TCDF, respectively. Automated dose-response modeling (ToxResponse Modeler) identified a total of 1027 and 837 genes with either a sigmoidal, exponential, linear, Gaussian, or quadratic dose-response relationship 72 h after treatment in TCDD and TCDF, respectively. Two hundred seventy genes exhibited a sigmoidal TCDD-induced dose-response (ED(50s) from 0.08 to 42.2 microg/kg) compared to only 179 sigmoidal responsive genes (ED(50s) from 0.74 to 299.9 microg/kg) elicited by TCDF. Of the 1027 TCDD dose-responsive genes, 654 were not examined further due to the lack of a dose response elicited by TCDF. Of the 373 genes that exhibited a TCDD and TCDF dose response, REPs were calculated for the 83 genes that exhibited comparable sigmoidal curve shapes and slopes. The median REP for these 83 genes was 0.10, with a maximum REP of 0.56 and a minimum of 0.01. REPs of 0.04 were also calculated for EROD and increase in relative liver weight (RLW) at 72 h. Collectively, the lower number of TCDF-induced genes compared to TCDD and the 0.04 REPs for EROD activity and increased RLW are not consistent with the TEF of 0.10 for the hepatotoxicity of TCDF in C57BL/6 mice at 72 h.

摘要

毒效当量因子(TEFs)是根据与 2,3,7,8-四氯二苯并对二恶英(TCDD)相比,个别适应性和毒性反应的相对效力(REP)值分配给类二恶英化学物质的。使用安捷伦 4x44K 寡核苷酸微阵列来检查 2,3,7,8-四氯二苯并呋喃(TCDF)相对于 TCDD 的肝基因表达效力,与互补的组织病理学、TCDD 和 TCDF 组织水平分析以及乙氧基Resorufin-O-脱乙基酶(EROD)测定数据相关。用 0.03、0.1、0.3、1、3、10、30 或 100μg/kg TCDD、世界卫生组织经 TEF 调整剂量(TCDD 剂量的 10 倍)的 TCDF(0.3、1、3、10、30、100 或 300μg/kg)或芝麻油载体对未成熟去卵巢 C57BL/6 小鼠进行灌胃,并在 72 小时后处死。TCDD 和 TCDF 分别在一个或多个剂量下使 2288 个和 1347 个基因发生差异表达(P1(t) > 0.90)。自动剂量反应建模(ToxResponse Modeler)在 TCDD 和 TCDF 处理后 72 小时,共鉴定出 1027 个和 837 个具有正弦、指数、线性、高斯或二次剂量反应关系的基因。与 TCDF 仅诱导 179 个具有正弦曲线形状和斜率的可诱导基因(ED(50s)从 0.74 到 299.9μg/kg)相比,270 个基因表现出 TCDD 诱导的正弦剂量反应(ED(50s)从 0.08 到 42.2μg/kg)。在 1027 个 TCDD 剂量反应基因中,由于缺乏 TCDF 引起的剂量反应,654 个基因未进一步研究。在表现出 TCDD 和 TCDF 剂量反应的 373 个基因中,计算了 83 个表现出可比正弦曲线形状和斜率的基因的 REP。这些 83 个基因的中位 REP 为 0.10,最大 REP 为 0.56,最小 REP 为 0.01。还计算了 72 小时时 EROD 和相对肝重(RLW)增加的 0.04 REP。总的来说,与 TCDD 相比,TCDF 诱导的基因数量较少,EROD 活性和 RLW 增加的 0.04 REP 与 TCDF 在 C57BL/6 小鼠中的 72 小时肝毒性的 0.10 TEF 不一致。

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