The ototoxicity of trichloroethylene: Extrapolation and relevance of high-concentration, short-duration animal exposure data

被引:29
作者
Crofton, KM [1 ]
Zhao, X [1 ]
机构
[1] MANTECH SCI INC,RES TRIANGLE PK,NC 27709
来源
FUNDAMENTAL AND APPLIED TOXICOLOGY | 1997年 / 38卷 / 01期
关键词
D O I
10.1006/faat.1997.2327
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Inhalation exposure to high concentrations of 1,1,2-trichloroethylene (TCE) has been shown to damage hearing in the mid-frequency range in the rat. The present study directly evaluated the adequacy of high-concentration, short-term exposures to TCE for predicting the neurotoxicity produced by longer duration exposures. Adult male Long-Evans rats (n = 10-12 per group) were exposed to TCE via inhalation (whole body) in 1-m(3) stainless steel how-through chambers for 6 hr/day, 5 days/week. The following exposures were used: 1 day (4000-8000 ppm), 1 week (1000-4000 ppm), 4 weeks (800-3200 ppm), and 13 weeks (800-3200 ppm). Ah-only exposed animals served as controls. Auditory thresholds were determined for a 16-kHz tone 3-5 weeks after exposure using reflex modification audiometry. Results replicated previous findings of a hearing loss at 16 kHz for all exposure durations. The dB15 concentrations (concentration that increases thresholds by 15 dB) for 16-kHz thresholds were 6218, 2992, 2592, and 2160 ppm for the 1-day, 1-week, 4-week and 13-week exposures, respectively. These data demonstrate that the ototoxicity of TCE was less than that predicted by a strict concentration x time relationship, These data also demonstrate that simple models of extrapolation (i.e., C x t = k, Haber's Law) overestimate the potency of TCE when extrapolating from short-duration to longer-duration exposures. Furthermore, these data suggest that, relative to ambient or occupational exposures, the ototoxicity of TCE in the rat is a high-concentration effect. (C) 1997 Society of Toxicology.
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页码:101 / 106
页数:6
相关论文
共 28 条
[1]  
ALBEE RR, 1994, TOXICOLOGIST, V14, P351
[2]  
American Conference of Governmental Industrial Hygienists [ACGIH, 1992, THRESH LIM VAL BIOL
[3]  
ARLIENSOBORG P, 1992, SOLVENT NEUROTOXICIT
[4]  
ATSDR [Agency for Toxic Substances and Disease Registry], 1993, TOX PROF TRICHL
[5]   REFERENCE DOSE (RFD) - DESCRIPTION AND USE IN HEALTH RISK ASSESSMENTS [J].
BARNES, DG ;
DOURSON, M .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1988, 8 (04) :471-486
[6]   TRIMETHYLTIN EFFECTS ON AUDITORY FUNCTION AND COCHLEAR MORPHOLOGY [J].
CROFTON, KM ;
DEAN, KF ;
MENACHE, MG ;
JANSSEN, R .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 105 (01) :123-132
[7]   MID-FREQUENCY HEARING-LOSS IN RATS FOLLOWING INHALATION EXPOSURE TO TRICHLOROETHYLENE - EVIDENCE FROM REFLEX MODIFICATION AUDIOMETRY [J].
CROFTON, KM ;
ZHAO, X .
NEUROTOXICOLOGY AND TERATOLOGY, 1993, 15 (06) :413-423
[8]   SOLVENT-INDUCED OTOTOXICITY IN RATS - AN ATYPICAL SELECTIVE MID-FREQUENCY HEARING DEFICIT [J].
CROFTON, KM ;
LASSITER, TL ;
REBERT, CS .
HEARING RESEARCH, 1994, 80 (01) :25-30
[9]   The impact of dose rate on the neurotoxicity of acrylamide: The interaction of administered dose, target tissue concentrations, tissue damage, and functional effects [J].
Crofton, KM ;
Padilla, S ;
Tilson, HA ;
Anthony, DC ;
Raymer, JH ;
MacPhail, RC .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 139 (01) :163-176
[10]  
CROFTON KM, 1993, P MIDW M ASS RES OT