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Developmental Exposure to Aroclor 1254 Produces Low-Frequency Alterations in Adult Rat Brainstem Auditory Evoked Responses
Authors:HERR, DAVID W.   GOLDEY, ELLEN S.   CROFTON, KEVIN M.
Affiliation:National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency Research Triangle Park, North Carolina 27711

Received January 17, 1996; accepted May 10, 1996

Abstract:
Developmental exposure of Long—Evans rats to 0, 1, 4,or 8 mg/kg/day Aroclor 1254 (A1254) from Gestational Day 6 throughPostnatal Day 21 produces an elevated behavioral threshold fora 1-kHz tone. Brahistem auditory evoked responses (BAERs) wereassessed in a subset of these animals (about 1 year old) usingfiltered clicks at 1 (65 and 80 dB SPL), 4 (60 and 80 dB SPL),16 (40 and 80 dB SPL), and 32 (40 and 80 dB SPL) kHz. Aroclor1254 decreased BAER amplitudes at 1 and 4 kHz, but not at 16or 32 kHz. A dose-related decrease in the baseline-to-peak P1Aamplitude was observed for the 1-kHz (80-dB) stimulus. Dosesof 1, 4, or 8 mg/kg/day A1254 decreased the peak-to-peak amplitudeof both P1AN1 and P1BN1 for a 1-kHz (80-dB) stimulus. Dosesof 4 and 8 mg/kg/day A1254 decreased the peak-to-peak amplitudeof N1P2 and P2N2 for a 4-kHz (60-dB) or 1-kHz (80-dB) stimulus.At 8 mg/kg/day, A1254 also increased the latency of peak P4at 1 kHz (65 dB). The decreases in peak P1A amplitudes are consistentwith a dysfunction of the cochlea and/or auditory nerve. Together,the data confirm that developmental exposure of rats to A1254produces a permanent low- to mid-frequency auditory dysfunctionand suggest a cochlear and/or auditory nerve site of action.
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