Gray Leon Earl, Barlow Norman J, Howdeshell Kembra L, Ostby Joseph S, Furr Johnathan R, Gray Clark L
Endocrinology Branch, RTD, NHEERL, ORD, USEPA, Research Triangle Park, North Carolina 27711, USA.
Toxicol Sci. 2009 Aug;110(2):411-25. doi: 10.1093/toxsci/kfp109. Epub 2009 May 29.
In the rat, some phthalates alter sexual differentiation at relatively low dosage levels by altering fetal Leydig cell development and hormone synthesis, thereby inducing abnormalities of the testis, gubernacular ligaments, epididymis, and other androgen-dependent tissues. In order to define the dose-response relationship between di(2-ethylhexyl) phthalate (DEHP) and the Phthalate Syndrome of reproductive alterations in F1 male rats, Sprague-Dawley (SD) rat dams were dosed by gavage from gestational day 8 to day 17 of lactation with 0, 11, 33, 100, or 300 mg/kg/day DEHP (71-93 males per dose from 12 to 14 litters per dose). Some of the male offspring continued to be exposed to DEHP via gavage from 18 days of age to necropsy at 63-65 days of age (PUB cohort; 16-20/dose). Remaining males were not exposed after postnatal day 17 (in utero-lactational [IUL] cohort) and were necropsied after reaching full maturity. Anogenital distance, sperm counts and reproductive organ weights were reduced in F1 males in the 300 mg/kg/day group and they displayed retained nipples. In the IUL cohort, seminal vesicle weight also was reduced at 100 mg/kg/day. In contrast, serum testosterone and estradiol levels were unaffected in either the PUB or IUL cohorts at necropsy. A significant percentage of F1 males displayed one or more Phthalate Syndrome lesions at 11 mg/kg/day DEHP and above. We were able to detect effects in the lower dose groups only because we examined all the males in each litter rather than only one male per litter. Power calculations demonstrate how using multiple males versus one male/litter enhances the detection of the effects of DEHP. The results at 11 mg/kg/day confirm those reported from a National Toxicology Program multigenerational study which reported no observed adverse effect levels-lowest observed adverse effect levels of 5 and 10 mg/kg/day DEHP, respectively, via the diet.
在大鼠中,一些邻苯二甲酸盐通过改变胎儿睾丸间质细胞的发育和激素合成,在相对较低的剂量水平下改变性别分化,从而导致睾丸、睾丸引带、附睾以及其他雄激素依赖组织出现异常。为了确定邻苯二甲酸二(2-乙基己基)酯(DEHP)与F1雄性大鼠生殖改变的邻苯二甲酸盐综合征之间的剂量反应关系,从妊娠第8天至哺乳期第17天,对斯普拉格-道利(SD)大鼠母鼠进行灌胃给药,剂量分别为0、11、33、100或300mg/kg/天的DEHP(每剂量组来自12至14窝,每组71-93只雄性)。部分雄性后代从18日龄开始继续通过灌胃接触DEHP,直至63-65日龄处死后进行尸检(青春期队列;每组16-20只)。其余雄性在出生后第17天之后不再接触DEHP(宫内-哺乳期[IUL]队列),达到完全成熟后进行尸检。300mg/kg/天组的F1雄性大鼠肛门与生殖器间距离、精子计数和生殖器官重量降低,且出现乳头保留现象。在IUL队列中,100mg/kg/天组的精囊重量也降低。相比之下,在尸检时,青春期队列或IUL队列中的血清睾酮和雌二醇水平均未受影响。在11mg/kg/天及以上剂量的DEHP作用下,相当比例的F1雄性大鼠出现一种或多种邻苯二甲酸盐综合征病变。我们之所以能够在较低剂量组检测到影响,是因为我们检查了每窝中的所有雄性大鼠,而不是每窝仅检查一只雄性大鼠。功效计算表明,与每窝检查一只雄性大鼠相比,检查多只雄性大鼠如何增强了对DEHP影响的检测能力。11mg/kg/天的结果证实了美国国家毒理学计划多代研究报告的结果,该研究报告称,通过饮食摄入DEHP时,未观察到有害作用水平和最低观察到有害作用水平分别为5和10mg/kg/天。