Crofton K M, Ding D, Padich R, Taylor M, Henderson D
Neurotoxicology Division, MD-74B, National Health and Environmental Effects Research Laboratory, US EPA, Research Triangle Park, NC 27711, USA.
Hear Res. 2000 Jun;144(1-2):196-204. doi: 10.1016/s0378-5955(00)00062-9.
Maternal exposure to polyhalogenated hydrocarbons results in early postnatal hypothyroxenemia and a low-frequency hearing loss in adult offspring (Goldey et al., 1995a. Toxicol. Appl. Pharmacol. 135, 67-76; Herr et al., 1996. Fundam. Appl. Toxicol. 33, 120-128). The purpose of the present work was to determine whether the site-of-action of this auditory impairment was within the cochlea. Primiparous Long-Evans rats were given daily oral doses of corn oil (control) or 8 mg/kg of the commercial PCB mixture Aroclor 1254 (A1254) from gestation day (GD) 6 through postnatal day (PND) 21. Auditory thresholds for 1-, 4-, 16-, and 40-kHz tones were assessed using reflex modification audiometry in young adult offspring on postnatal days (PND) 92-110. Approximately 6 weeks after auditory assessments, a subset of animals (n=4 per group) were killed for histological assessment of the cochlea. Surface preparations of the organ of Corti were prepared from one cochlea per animal and modiolar sections were prepared from the opposite cochlea. Consistent with previous findings, auditory thresholds for 1-kHz tones were elevated by approximately 25 dB in the A1254-exposed animals. Thresholds for all higher frequencies were not different compared to controls. Surface preparations of the organ of Corti revealed a mild to moderate loss of outer hair cells in the upper-middle and apical turns. Inner hair cells were not affected. Modiolar sections failed to reveal alterations in any other cochlear structures. There was also no apparent loss of ganglion cells. These data clearly link the loss of low-frequency hearing caused by exposure during development to A1254 to a loss of outer hair cells in the organ of Corti. The mechanism that underlies this developmental ototoxicity remains to be determined. These data provide the first evidence of a structural deficit in the nervous system of adult animals exposed to PCBs during development.
母体接触多卤代烃会导致产后早期甲状腺素血症以及成年后代出现低频听力损失(戈尔迪等人,1995年a。《毒理学与应用药理学》135卷,67 - 76页;赫尔等人,1996年。《基础与应用毒理学》33卷,120 - 128页)。本研究的目的是确定这种听觉损伤的作用部位是否在耳蜗内。初产的长 - 伊文斯大鼠从妊娠第6天(GD)到出生后第21天(PND)每天经口给予玉米油(对照)或8毫克/千克的商业多氯联苯混合物氯丹1254(A1254)。在出生后第92 - 110天,使用反射修正听力测定法评估年轻成年后代对1、4、16和40千赫音调的听觉阈值。在听觉评估大约6周后,处死一部分动物(每组n = 4)用于耳蜗的组织学评估。从每只动物的一个耳蜗制备柯蒂氏器的表面标本,从相对的耳蜗制备蜗轴切片。与先前的研究结果一致,暴露于A1254的动物对1千赫音调的听觉阈值升高了约25分贝。与对照组相比,所有更高频率的阈值没有差异。柯蒂氏器的表面标本显示,中上部和顶部螺旋的外毛细胞有轻度至中度损失。内毛细胞未受影响。蜗轴切片未显示耳蜗其他结构有改变。神经节细胞也没有明显损失。这些数据清楚地将发育过程中暴露于A1254所导致的低频听力损失与柯蒂氏器中外毛细胞的损失联系起来。这种发育性耳毒性的潜在机制仍有待确定。这些数据首次证明了发育过程中接触多氯联苯的成年动物神经系统存在结构缺陷。