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吸入间二甲苯对大鼠异生物质代谢的剂量相关效应。

Dose-related effects of m-xylene inhalation on the xenobiotic metabolism of the rat.

作者信息

Elovaara E

出版信息

Xenobiotica. 1982 Jun;12(6):345-52. doi: 10.3109/00498258209052474.

Abstract
  1. Male Wistar rats were exposed for two weeks (6 h/d, 5 d/week) to 0, 50, 400 or 750 p.p.m. of m-xylene vapour in the air. 2. Microsomal enzyme activities were significantly increased in the liver as follows: NADPH-cytochrome c reductase (less than or equal to 1.2-fold), O-deethylation reactions (less than or equal to 1.8-fold) and UDP-glucuronosyltransferase activity (less than or equal to 2.9-fold). Cytochrome P-450 concentrations also increased with dose. 3. Microsomal affinity to m-xylene increased with dose of m-xylene in vivo, similar to the increased affinity seen in type I spectra390-420nm formation with cytochrome P-450 in vitro. 4. Reduced glutathione concn. in liver declined significantly, while in the kidneys the glutathione remained unchanged. 5. In the kidneys, the concn. of cytochrome P-450 (less than or equal to 1.3-fold), O-deethylation activity (less than or equal to 5.3-fold) and the rate of glucuronidation (less than or equal to 1.8-fold) increased with the dose of xylene. 6. Microsomal protein contents in liver and kidneys increased with the two highest doses of xylene. 7. The hepatic and renal effects were dose-dependent and closely related to the accumulation of m-xylene in perirenal fat. 8. Despite stimulation of xenobiotic metabolism by m-xylene, inhalation did not alter the serum transaminase activity or cause morphological changes in the liver.
摘要
  1. 将雄性Wistar大鼠暴露于空气中0、50、400或750 ppm的间二甲苯蒸气中两周(每天6小时,每周5天)。2. 肝脏中的微粒体酶活性显著增加如下:NADPH - 细胞色素c还原酶(≤1.2倍)、O - 脱乙基反应(≤1.8倍)和UDP - 葡萄糖醛酸基转移酶活性(≤2.9倍)。细胞色素P - 450浓度也随剂量增加。3. 微粒体对间二甲苯的亲和力在体内随间二甲苯剂量增加,类似于体外细胞色素P - 450在390 - 420nm形成I型光谱时所见的亲和力增加。4. 肝脏中还原型谷胱甘肽浓度显著下降,而肾脏中的谷胱甘肽保持不变。5. 在肾脏中,细胞色素P - 450浓度(≤1.3倍)、O - 脱乙基活性(≤5.3倍)和葡萄糖醛酸化速率(≤1.8倍)随二甲苯剂量增加。6. 肝脏和肾脏中的微粒体蛋白含量随二甲苯的两个最高剂量增加。7. 肝脏和肾脏的效应呈剂量依赖性,且与间二甲苯在肾周脂肪中的蓄积密切相关。8. 尽管间二甲苯刺激了异源物质代谢,但吸入并未改变血清转氨酶活性或引起肝脏形态学变化。

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