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Early differential gene expression of rat lung after exposure to paraquat.

机译:暴露于百草枯后大鼠肺的早期差异基因表达。

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Paraquat (PQ), a quaternary nitrogen herbicide, is highly toxic to humans and animals. Acute poisoning and death due to PQ exposure have been reported over the past few decades. Excessive production of oxygen free radicals has been proposed to play an important role in the pulmonary pathology. The aim of the present work was to evaluate the implications for genes that are regulated by oxidative stress at the early stage of PQ exposure in rat lungs. We performed differential display RT-PCR (DD-PCR) on total RNA extracted from rat lungs after injection of 20mg per kg body weight. The experimental DD-PCR conditions, primer length and annealing temperature, were adjusted to improve reproducibility, and 19 differentiated clones were isolated. Sequence analysis followed by conventional RT-PCR and real-time RT-PCR analyses were used to confirm the results. Four clones were finally determined to be significantly affected. These genes were mRNAs for plasma phospholipid transfer protein (PLTP), CL1BA protein, (latrophilin: LPH), and alphaII-spectrin as well as one unknown gene. We demonstrated the distribution of mRNA expression of one gene, LPH, in lung tissues. The present study suggests that 20mg per kg intraperitoneal PQ affects the expression of numerous genes in the lung at 3 h, the onset of pulmonary injury, and that the four genes specified may be major contributors to serious lung injury due to PQ exposure.
机译:百草枯(PQ)是一种季氮除草剂,对人和动物具有剧毒。在过去的几十年中,已经报道了由于暴露于PQ而引起的急性中毒和死亡。已经提出过量产生氧自由基在肺病理中起重要作用。本研究的目的是评估在大鼠肺部PQ暴露早期受氧化应激调节的基因的意义。在注射每公斤体重20mg后,我们对从大鼠肺中提取的总RNA进行了差异显示RT-PCR(DD-PCR)。调节实验DD-PCR条件,引物长度和退火温度以提高可重复性,并分离出19个分化的克隆。序列分析后进行常规RT-PCR和实时RT-PCR分析,以确认结果。最终确定四个克隆受到显着影响。这些基因是血浆磷脂转移蛋白(PLTP),CL1BA蛋白,(latrophilin:LPH)和alphaII-spectrin的mRNA,以及一个未知基因。我们证明了肺组织中一种基因LPH的mRNA表达的分布。本研究表明,腹膜内PQ 20mg / kg会影响3h肺损伤中肺中众多基因的表达,并且指定的四个基因可能是由于PQ暴露导致严重肺损伤的主要因素。

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