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使用DNA微阵列对小鼠肝脏中伯氨喹诱导的差异基因表达进行分析。

Primaquine-induced differential gene expression analysis in mice liver using DNA microarrays.

作者信息

Noel Sanjeev, Sharma Sharad, Shanker Rishi, Rath Srikanta Kumar

机构信息

Division of Toxicology, Central Drug Research Institute, M G Marg, Lucknow, India.

出版信息

Toxicology. 2007 Sep 24;239(1-2):96-107. doi: 10.1016/j.tox.2007.06.098. Epub 2007 Jul 1.

Abstract

Primaquine (PQ), a clinically important derivative of 8-aminoquinoline used against the hepatic stages (hypnozoites) of Plasmodium vivax and Plasmodium ovale, was studied to evaluate and compare between mRNA expression, and biochemical and histological parameters of hepatic stress in adult Swiss mice (Mus musculus). Following single oral dose of PQ (40 mg/kg, bw), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) along with hematoxylin and eosin stained liver sections did not show any signs of hepatic stress at 6, 12 and 24 h except for ALT activity at 6h. However, analysis at RNA transcript level revealed consistent and significant deregulation (p<0.01 and two-fold) of 16 probes corresponding to important cellular processes such as protein transportation, transcription regulation, intracellular signaling, protein synthesis, hematopoiesis, cell adhesion and cell proliferation. Pathway analysis identified large number of affected genes corresponding to 40 Gene Ontology terms having a z score greater than 2. These results indicate that PQ at high doses may affect gene expression in liver and may produce undesirable outcomes if consumed for longer durations.

摘要

伯氨喹(PQ)是一种临床上重要的8-氨基喹啉衍生物,用于对抗间日疟原虫和卵形疟原虫的肝期(休眠子)。本研究旨在评估和比较成年瑞士小鼠(小家鼠)肝脏应激的mRNA表达、生化及组织学参数。单次口服PQ(40 mg/kg,体重)后,在6、12和24小时时,丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)以及苏木精-伊红染色的肝脏切片均未显示出任何肝脏应激迹象,但6小时时ALT活性除外。然而,RNA转录水平分析显示,对应于蛋白质运输、转录调控、细胞内信号传导、蛋白质合成、造血、细胞粘附和细胞增殖等重要细胞过程的16个探针出现了持续且显著的失调(p<0.01且为两倍)。通路分析确定了大量受影响的基因,对应于40个z评分大于2的基因本体术语。这些结果表明,高剂量的PQ可能会影响肝脏中的基因表达,如果长期服用可能会产生不良后果。

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