Subchronic delayed neurotoxicity evaluation of jet engine lubricants containing phosphorus additives

被引:14
作者
Daughtrey, W
Biles, R
Jortner, B
Ehrlich, M
机构
[1] EXXON CO USA,HOUSTON,TX 77002
[2] VIRGINIA POLYTECH INST & STATE UNIV,VIRGINIA MARYLAND REG COLL VET MED,BLACKSBURG,VA 24061
来源
FUNDAMENTAL AND APPLIED TOXICOLOGY | 1996年 / 32卷 / 02期
关键词
D O I
10.1006/faat.1996.0127
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Synthetic polyol-based lubricating oils containing 3% of either commercial tricresyl phosphate (TCP), triphenylphosphorotihionate (TPPT), or butylated triphenyl phosphate (BTP) additive were evaluated for neurotoxicity in the adult hen using clinical, biochemical, and neuropathological endpoints. Groups of 17-20 hens were administered the oils by oral gavage at a ''limit dose'' of a g/kg, 5 days a week for 13 weeks. A group of positive control hens was included which received 7.5 mg/kg of one isomer of TCP (tri-ortho-cresyl phosphate, TOCP) on the same regimen, with an additional oral dose of 580 mg/kg given 12 clays before the end of the experiment. A negative control group received saline. Neurotoxic esterase (NTE) activity in brain and spinal cord. of hens dosed with the lubricating oils was not significantly different from saline controls after 6 weeks of treatment. After 13 weeks of dosing, NTE was inhibited 23 to 34% in brains of lubricant-treated hens. Clinical assessments of walking ability did not indicate any differences between the negative control group and lubricant-treated hens. Moreover, neuropathological examination revealed no alterations indicative of organophosphorus-induced delayed neuropathy (OPIDN). In hens treated with the positive control, significant inhibition of NTE was observed in brain and spinal cord at both 6 and 13 weeks of dosing; this group also demonstrated clinical impairment and pathological lesions indicative of OPIDN, In conclusion, the results of the present study indicated that synthetic polyol-based lubricating oils containing up to 3% TCP, TPPT, or BTP had low neural oxic potential and should not pose a hazard under realistic conditions of exposure. (C) 1996 Society of Toxicology
引用
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页码:244 / 249
页数:6
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