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有机硫化合物对大鼠微粒体环氧化物水解酶基因表达的增强作用。

Enhanced expression of rat microsomal epoxide hydrolase gene by organosulfur compounds.

作者信息

Kim N D, Kim S G, Kwak M K

机构信息

College of Pharmacy, Seoul National University, Korea.

出版信息

Biochem Pharmacol. 1994 Feb 9;47(3):541-7. doi: 10.1016/0006-2952(94)90186-4.

Abstract

The effects of organosulfur compounds including allylsulfide (AS), allylmercaptan (AM) and allylmethylsulfide (AMS) on the expression of microsomal epoxide hydrolase (mEH) protein and its mRNA were examined in rats. The levels of mEH induction were examined with or without concomitant treatment of animals with pyrazine, a strong inducer of mEH, in order to establish whether a common molecular basis exists for mEH induction between these structurally different xenobiotics. Immunoblot analyses using anti-rat mEH antibody showed that treatment with AS caused an approximately 4-fold increase in hepatic mEH protein levels relative to controls whereas treatment with both AS and pyrazine resulted in only minimal additive increases in the elevation of mEH. Administration of AM to rats resulted in a comparable increase in mEH levels to that caused by AS, whereas an approximately 2-fold increase was noted after AMS treatment, as compared to control. mEH levels in the hepatic microsomes isolated from animals treated with both AMS and pyrazine were, however, approximately 50% less than those from pyrazine-treated rats. Thus, AS and AM appeared to be more effective than AMS in elevating mEH, as evidenced by immunoblot analyses. The levels of mEH mRNA were increased 10-16-fold following treatment with either AS or AM, while AMS caused a 3-7-fold increase relative to control, as assessed by slot blot analysis probed with a 1.3 kb mEH cDNA. Time-dependent increases in mRNA levels by each of these organosulfur compounds were consistent with those in mEH protein levels at 3 days. A marginal additive increase in mEH mRNA levels was noted following co-administration of either AS or AM with pyrazine, whereas treatment with both AMS and pyrazine decreased mEH mRNA levels by 55%. Significant mEH mRNA increases in poly(A)+ RNA fractions were confirmed by northern blot analysis. The results demonstrate that these organosulfur compounds are inducers of mEH and that the induction involves increases in its mRNA.

摘要

在大鼠中研究了包括烯丙基硫醚(AS)、烯丙基硫醇(AM)和烯丙基甲基硫醚(AMS)在内的有机硫化合物对微粒体环氧化物水解酶(mEH)蛋白及其mRNA表达的影响。为了确定这些结构不同的外源化合物之间mEH诱导是否存在共同的分子基础,在动物同时或不同时用吡嗪(一种mEH的强诱导剂)处理的情况下,检测mEH的诱导水平。使用抗大鼠mEH抗体的免疫印迹分析表明,与对照组相比,AS处理使肝脏mEH蛋白水平增加了约4倍,而AS和吡嗪共同处理仅导致mEH升高的最小累加增加。给大鼠施用AM导致mEH水平的增加与AS引起的增加相当,而与对照组相比,AMS处理后mEH水平增加了约2倍。然而,从同时用AMS和吡嗪处理的动物分离的肝微粒体中的mEH水平比吡嗪处理的大鼠低约50%。因此,免疫印迹分析表明,AS和AM在升高mEH方面似乎比AMS更有效。用1.3 kb mEH cDNA探针进行斑点印迹分析评估,AS或AM处理后mEH mRNA水平增加了10 - 16倍,而AMS相对于对照组引起了3 - 7倍的增加。这些有机硫化合物各自导致的mRNA水平随时间的增加与3天时mEH蛋白水平的增加一致。AS或AM与吡嗪共同给药后,mEH mRNA水平有轻微的累加增加,而AMS和吡嗪共同处理使mEH mRNA水平降低了55%。通过Northern印迹分析证实了多聚腺苷酸(poly(A)+)RNA组分中mEH mRNA的显著增加。结果表明,这些有机硫化合物是mEH的诱导剂,并且诱导涉及mRNA的增加。

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