用多氯联苯126和多氯联苯153混合物处理后大鼠肝脏中CYP1A1的区域诱导作用

Regional induction of CYP1A1 in rat liver following treatment with mixtures of PCB 126 and PCB 153.

作者信息

Chubb Laura S, Andersen Melvin E, Broccardo Carolyn J, Legare Marie E, Billings Ruth E, Dean Charles E, Hanneman William H

机构信息

Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado 80523-1680, USA.

出版信息

Toxicol Pathol. 2004 Jul-Aug;32(4):467-73. doi: 10.1080/01926230490483306.

Abstract

Liver enzyme induction has been shown previously to be regional with clear borders between induced and uninduced regions in vivo, and cells either fully induced or not induced in vitro. The current study examined this phenomenon in vivo by evaluating enzyme induction after exposure to PCB 126 and PCB 153 in female Fisher 344 (F344) and male Sprague-Dawley (SD) rats. IHC revealed a regional induction of CYP1A1 after exposure to PCB 126, apparent in the centrilobular region at lower doses and progressing to panlobular with higher doses. PCB 153 exposure induced CYP2B1/2 in the centrilobular region, which spread to the midzonal region as the dose increased, but never became panlobular even at the highest dosage tested. In rats treated with PCB 126 in combination with high doses of PCB 153, induction of CYP1A1 occurred preferentially in the periportal region, a reversal from the pattern seen with PCB 126 alone. This CYP1A1 induction pattern reversal is a unique example of complex biological interactions between coplanar (PCB 126) and noncoplanar (PCB 153) halogenated aromatic hydrocarbons.

摘要

先前已表明,肝脏酶诱导在体内具有区域性,诱导区域和未诱导区域之间有清晰的边界,并且细胞在体外要么完全被诱导,要么未被诱导。当前研究通过评估雌性费希尔344(F344)大鼠和雄性斯普拉格-道利(SD)大鼠暴露于多氯联苯126(PCB 126)和多氯联苯153(PCB 153)后的酶诱导情况,在体内研究了这一现象。免疫组化显示,暴露于PCB 126后,CYP1A1呈区域性诱导,低剂量时在小叶中心区域明显,高剂量时发展为全小叶诱导。暴露于PCB 153会在小叶中心区域诱导CYP2B1/2,随着剂量增加,其会扩散到中区区域,但即使在测试的最高剂量下也从未发展为全小叶诱导。在用PCB 126与高剂量PCB 153联合处理的大鼠中,CYP1A1的诱导优先发生在门静脉周围区域,这与单独使用PCB 126时的模式相反。这种CYP1A1诱导模式的逆转是共面(PCB 126)和非共面(PCB 153)卤代芳烃之间复杂生物相互作用的一个独特例子。

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