Dent J G
Environ Health Perspect. 1978 Apr;23:301-7. doi: 10.1289/ehp.7823301.
The mixture of PBBs in FireMaster BP-6 has been demonstrated to constitute potent inducers of hepatic and extrahepatic mixed function oxidase (MFO) enzymes. Chronic dietary administration of PBBs to mature female rats results in a "mixed" pattern of induction, with increases in both cytochrome P-450 and P1-450 associated enzymes. Acute administration of PBBs (150 mg/kg IP) to mature female rats resulted in a time-dependent induction of MFO activities; the P-450-dependent enzymes were simulated early (24-48 hr after administration) while the P1-450 dependent enzymes reached maximal activities at later time points. However, studies of the kinetics and patterns of inhibition of the induced enzymes along with gel electrophoresis studies of the microsomal proteins indicate that PBBs may induce different proteins from those induced by the classical P-450 and P1-450 inducers, phenobarbital and 3-methylcholanthrene. In addition, the pattern of enzyme induction caused by PBBs in developing rats differs from that in adults, in that the P1-450-associated enzymes are stimulated prior to the P-450-associated enzymes. The overall pattern of enzyme induction in extrahepatic tissue differs from that seen in the liver and sex differences in enzyme induction have also been demonstrated. As modifications of MFO activity may alter the toxicity of chemicals, these findings suggest that the toxicity of chemicals may be altered in animals exposed to PBBs and that these toxicities may exhibit age, sex, and organ specificities different from those seen in control animals.
已证明FireMaster BP - 6中的多溴联苯混合物是肝脏和肝外混合功能氧化酶(MFO)的强效诱导剂。对成年雌性大鼠长期进行多溴联苯的饮食给药会导致一种“混合”诱导模式,细胞色素P - 450和P1 - 450相关酶均增加。对成年雌性大鼠急性给予多溴联苯(150 mg/kg腹腔注射)会导致MFO活性随时间依赖性诱导;P - 450依赖性酶在给药后早期(24 - 48小时)被诱导,而P1 - 450依赖性酶在后期时间点达到最大活性。然而,对诱导酶的抑制动力学和模式的研究以及微粒体蛋白的凝胶电泳研究表明,多溴联苯可能诱导出与经典的P - 450和P1 - 450诱导剂(苯巴比妥和3 - 甲基胆蒽)不同的蛋白质。此外,多溴联苯在发育中的大鼠中引起的酶诱导模式与成年大鼠不同,即P1 - 450相关酶在P - 450相关酶之前被刺激。肝外组织中酶诱导的总体模式与肝脏中所见不同,并且也已证明酶诱导存在性别差异。由于MFO活性的改变可能会改变化学物质的毒性,这些发现表明,在接触多溴联苯的动物中,化学物质的毒性可能会改变,并且这些毒性可能表现出与对照动物不同的年龄、性别和器官特异性。