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利用DNA微阵列技术对链脲佐菌素处理的小鼠肝脏进行基因表达谱分析。

Gene expression profiling in streptozotocin treated mouse liver using DNA microarray.

作者信息

Kume Eisuke, Aruga Chinami, Ishizuka Yukito, Takahashi Kaori, Miwa Satoko, Itoh Masahito, Fujimura Hisako, Toriumi Wataru, Kitamura Kazuyuki, Doi Kunio

机构信息

Exploratory Toxicology and DMPK Research Laboratory, Tanabe Seiyaku Co Ltd, 2-2-50, Kawagishi, Toda, Saitama 335, Japan.

出版信息

Exp Toxicol Pathol. 2005 Mar;56(4-5):235-44. doi: 10.1016/j.etp.2004.09.002.

Abstract

Streptozotocin (SZ) is known to exert toxic effects not only on pancreatic islet beta cells but also on other organs including liver. For analyzing changes in genes expression associated with SZ toxicity, we performed DNA microarray analyses on the liver obtained from SZ-treated mice. Eight-week-old male ICR mice were treated i.p. with 200 mg/kg of SZ, and the blood and liver were taken at 6, 24 and 48 h after the treatment. Labeled cRNA prepared from total RNA of the liver was hybridized to the GeneChip Murine Genome U74A V.2 (Affymetrix). The number of the probe sets, which were clearly up-regulated or down-regulated, were over 100 at 6 and 24h after the SZ-treatment, and it decreased at 48 h after the treatment. Many of the up-regulated genes were categorized into cell cycle/apoptosis related genes, immune/allergy related genes and stress response/xenobiotic metabolism related genes. On the other hand, genes related to glucose, lipid and protein metabolisms were down-regulated. These changes started prior to the elevation of the serum glucose levels, indicating the direct action of SZ on the liver rather than the secondary effect of diabetes. This may be related with the previously reported hepatic changes such as lipid peroxidation, mitochondrial swelling and inhibition of hepatocyte proliferation observed before the development of hyperglycemia.

摘要

链脲佐菌素(SZ)不仅对胰岛β细胞有毒性作用,对包括肝脏在内的其他器官也有毒性作用。为了分析与SZ毒性相关的基因表达变化,我们对经SZ处理的小鼠的肝脏进行了DNA微阵列分析。8周龄雄性ICR小鼠腹腔注射200mg/kg的SZ,并在处理后6、24和48小时采集血液和肝脏。从肝脏总RNA制备的标记cRNA与基因芯片小鼠基因组U74A V.2(Affymetrix)杂交。在SZ处理后6小时和24小时,明显上调或下调的探针集数量超过100个,在处理后48小时减少。许多上调基因被归类为细胞周期/凋亡相关基因、免疫/过敏相关基因和应激反应/异生物质代谢相关基因。另一方面,与葡萄糖、脂质和蛋白质代谢相关的基因被下调。这些变化在血清葡萄糖水平升高之前就开始了,表明SZ对肝脏有直接作用,而不是糖尿病的继发效应。这可能与先前报道的在高血糖发生之前观察到的肝脏变化有关,如脂质过氧化、线粒体肿胀和肝细胞增殖抑制。

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