Espandiari P, Thomas V A, Glauert H P, O'Brien M, Noonan D, Robertson L W
Department of Nutrition and Food Science, University of Kentucky, Lexington 40506-0054, USA.
Fundam Appl Toxicol. 1995 Jun;26(1):85-90. doi: 10.1006/faat.1995.1077.
The widely used broad leaf herbicide, dicamba, or Banvel, is similar in structure to xenobiotics which induce hepatic drug metabolism or proliferation of hepatic peroxisomes in rodents. The ability of xenobiotics to effect these hepatic changes often portends their positive outcomes in chronic bioassays. Dicamba's ability to induce hepatomegaly and peroxisome proliferation was studied in male and female Sprague-Dawley rats. Rats were placed on feed containing 0, 0.001, 0.01, 0.1, or 1% dicamba or 0.01% ciprofibrate for 3 weeks. Dicamba had no effect on relative liver weights or feed efficiency in either female or male rats at all doses tested. Dicamba, however, caused a statistically significant increase in peroxisomal beta-oxidation activity in liver homogenates from rats of both sexes fed 1% dicamba. Fatty acyl CoA-oxidase activity was increased in male rats fed 1% dicamba. A protein of M(r) 80 kDa was visible when liver homogenates of female or male rats fed 1% dicamba were subjected to SDS-PAGE. Lauric acid hydroxylase activity and CYP4A-reactive protein were increased in microsomes from male rats fed the highest level of dicamba. Moreover, dicamba was observed to transcriptionally upregulate the peroxisome proliferator-activated receptor (PPAR), a peroxisome proliferator sensitive receptor previously shown to be linked to the transcriptional regulation of a variety of peroxisome-specific enzymes. These studies show that dicamba is a peroxisome proliferator in rats. Although dicamba was not an efficacious inducer of peroxisomal enzymes in these rats, dicamba's ability to transcriptionally activate the PPAR and induce peroxisomal and related enzymes must be considered in the safety evaluation of this herbicide.
广泛使用的阔叶除草剂麦草畏(又称百草敌),其结构与能诱导啮齿动物肝脏药物代谢或肝脏过氧化物酶体增殖的异生素相似。异生素引发这些肝脏变化的能力往往预示着它们在慢性生物测定中的阳性结果。我们研究了麦草畏在雄性和雌性斯普拉格-道利大鼠中诱导肝肿大和过氧化物酶体增殖的能力。将大鼠置于含有0、0.001%、0.01%、0.1%或1%麦草畏或0.01%环丙贝特的饲料中喂养3周。在所有测试剂量下,麦草畏对雌性或雄性大鼠的相对肝脏重量或饲料效率均无影响。然而,给雌雄大鼠喂食1%麦草畏后,其肝脏匀浆中的过氧化物酶体β-氧化活性出现了统计学上的显著增加。给雄性大鼠喂食1%麦草畏后,脂肪酰基辅酶A氧化酶活性增加。当给雌雄大鼠喂食1%麦草畏后的肝脏匀浆进行SDS-PAGE时,可见一条分子量为80 kDa的蛋白质条带。给雄性大鼠喂食最高剂量麦草畏后,微粒体中的月桂酸羟化酶活性和CYP4A反应性蛋白增加。此外,还观察到麦草畏能转录上调过氧化物酶体增殖物激活受体(PPAR),此前已证明该过氧化物酶体增殖物敏感受体与多种过氧化物酶体特异性酶的转录调控有关。这些研究表明,麦草畏在大鼠中是一种过氧化物酶体增殖剂。尽管在这些大鼠中麦草畏不是过氧化物酶体酶的有效诱导剂,但在对这种除草剂进行安全性评估时,必须考虑麦草畏转录激活PPAR以及诱导过氧化物酶体和相关酶的能力。