Chinje E, Kentish P, Jarnot B, George M, Gibson G
Molecular Toxicology Group, School of Biological Sciences, University of Surrey, Guildford, UK.
Toxicol Lett. 1994 Mar;71(1):69-75. doi: 10.1016/0378-4274(94)90200-3.
Male Wistar rats and male Duncan Hartley guinea pigs were treated with one i.p. dose of perfluorodecanoic acid (PFDA) resulting in pronounced hepatomegaly in the rat but not the guinea pig. PFDA treatment also resulted in a 4-fold induction of lauric acid 12-hydroxylase activity in the rat but not the guinea pig, indicating induction of the CYP4A subfamily of isoenzymes. Consistent with this latter conclusion, Western blot analysis of rat liver microsomes using an antibody to CYP4A1 and Northern blot analysis of RNA extracts using a CYP4A1 cDNA probe, revealed PFDA-dependent induction of the CYP4A subfamily in the rat but not the guinea pig. Taken collectively, our data has demonstrated that PFDA, like other peroxisome proliferators, is also a CYP4A inducer and conforms to the well-documented species specificity in induction for this class of compound.
雄性Wistar大鼠和雄性Duncan Hartley豚鼠经腹腔注射一剂全氟癸酸(PFDA)进行处理,结果大鼠出现明显的肝肿大,而豚鼠未出现。PFDA处理还导致大鼠月桂酸12-羟化酶活性诱导增加4倍,而豚鼠未出现这种情况,这表明细胞色素P450 4A(CYP4A)同工酶亚家族被诱导。与后一结论一致,使用针对CYP4A1的抗体对大鼠肝微粒体进行蛋白质免疫印迹分析,以及使用CYP4A1 cDNA探针对RNA提取物进行Northern印迹分析,结果显示PFDA可诱导大鼠而非豚鼠的CYP4A亚家族。综合来看,我们的数据表明,PFDA与其他过氧化物酶体增殖剂一样,也是一种CYP4A诱导剂,并且符合这类化合物诱导作用中充分记录的物种特异性。