丁基羟基甲苯对大鼠的发育性神经行为毒性

C.V. Vorhees , R.E. Butcher , R.L. Brunner , T.J. Sobotka
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引用次数: 27

摘要

将丁基羟基甲苯(BHT)按0、0·125、0·25%或0·5% (w/w)的水平饲喂于大鼠的整个发育过程(从受孕前到出生后第90天)。阳性对照组在妊娠第12天注射抗有丝分裂/胚胎毒性药物羟基脲550 mg/kg作为对照。所有组的后代均由其天然母坝饲养,并在出生后第3天至第90天进行一系列行为测试。饲粮中添加0.5%的BHT可降低母鼠和后代在早期发育期间的体重,并增加30日龄前的后代死亡率(高达39%)。该剂量延迟了男性的眼睑打开、表面矫正发育和游泳时的肢体协调,并减少了女性的野外活动;然而,断奶后没有发现明显的影响。低剂量BHT对母鼠体重有一定影响(增加0.25%,减少0.125%),但对后代体重没有影响。0.25%的BHT增加了断奶前和围断奶期的死亡率(23%),但该剂量和0.125%的BHT对身体或行为发育以及断奶后的行为表现都没有任何影响。经羟基脲治疗的阳性对照组断奶前生长发育减慢,成人脑重量减轻,断奶前和围断奶期死亡率略有但不显著增加(10%)。这一组在游泳时也表现出眼睑打开延迟,向前运动发育和肢体协调延迟,但对断奶后的行为表现没有影响。BHT的研究结果与现有的毒理学文献一致,即BHT对生长中的啮齿动物在剂量为饮食的0.25%或0.5%时具有毒性,在剂量为饮食的0.125%时具有边际效应。行为数据扩展了BHT毒性的图像,但没有表明BHT对中枢神经系统有任何不成比例的或特殊的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental neurobehavioural toxicity of butylated hydroxytoluene in rats

Butylated hydroxytoluene (BHT) was fed to rats throughout development (from before conception through to day 90 of postnatal life) at levels of 0, 0·125, 0·25 or 0·5% (w/w) in the diet. A similarly treated positive control group was injected on day 12 of gestation with 550 mg/kg of the antimitotic/embryotoxic drug hydroxyurea for reference. Offspring from all groups were reared by their natural dams and were evaluated in a battery of behavioural tests from day 3 to day 90 after birth. BHT at 0·5% in the diet reduced the body weights of dams and of offspring during early development and increased offspring mortality (to 39%) up to 30 days of age. This dose delayed eyelid opening, surface-righting development and limb co-ordination in swimming in males, and reduced female open-field ambulation; however, no significant effects were found after weaning. The lower doses of BHT produced some irregularities in maternal weight (0·25% an increase and 0·125% a decrease) but had no effect on the body weights of offspring. BHT at 0·25% of the diet increased pre- and periweaning mortality (23%), but neither this dose nor the 0·125% dose had any effect on physical or behavioural development or on post-weaning behavioural performance. The positive control group treated with hydroxyurea showed reduced growth prior to weaning, reduced adult brain weight and a slight but nonsignificant increase in pre- and periweaning mortality (10%). This group also exhibited delayed eyelid opening, delayed forward locomotor development and limb co-ordination during swimming, but showed no effects on postweaning behavioural performance. The BHT findings are consistent with the existing toxicological literature that BHT is toxic to growing rodents at doses of 0·25 or 0·5% of the diet with marginal effects at 0·125% of the diet. The behavioural data expand the picture of BHT's toxicity, but do not suggest any disproportionate or special toxicity of BHT for the central nervous system.

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