Gagnaire F, Ensminger A, Marignac B, De Ceaurriz J
Institut National de Recherche et de Sécurité, Vandoeuvre, France.
J Appl Toxicol. 1991 Aug;11(4):261-8. doi: 10.1002/jat.2550110406.
The role of 1,2-diacetylbenzene (1,2-DAB) in the peripheral nerve toxicity of 1,2-diethylbenzene (1,2-DEB) was investigated in rats. Gas chromatography-mass spectrometry identified 1,2-DAB in the urine samples of rats given 165 mg kg-1 1,2-DEB orally on four consecutive days. 1,2-DAB shared not only the ability of 1,2-DEB to cause bluish discoloration of skin, internal organs and urine, but unlike 1,2-DEB it turned hair blue at the site of intraperitoneal injection. Intraperitoneal administration of 10 mg kg-1 and 20 mg kg-1 1,2-DAB to groups of 12 rats, 4 days a week for 11 and 6 weeks, caused a dose- and time-dependent decrease in mean sensory and motor conduction velocities. Recovery in a 5-week post-exposure period was gradual but consistent. The effect of 1,2-DAB on the amplitude of the sensory action potential was ambiguous. The findings support the hypothesis that the formation of 1,2-diacetylbenzene derivatives contributes to the neurotoxicity of 1,2-DEB.
研究了1,2 - 二乙酰苯(1,2 - DAB)在1,2 - 二乙苯(1,2 - DEB)对大鼠周围神经毒性中的作用。气相色谱 - 质谱法在连续四天口服给予165 mg kg-1 1,2 - DEB的大鼠尿液样本中鉴定出1,2 - DAB。1,2 - DAB不仅具有1,2 - DEB使皮肤、内脏器官和尿液变蓝的能力,但与1,2 - DEB不同的是,它会使腹腔注射部位的毛发变蓝。对12只大鼠组成的几组进行腹腔注射10 mg kg-1和20 mg kg-1的1,2 - DAB,每周4天,持续11周和6周,导致平均感觉和运动传导速度呈剂量和时间依赖性下降。暴露后5周的恢复期是渐进但持续的。1,2 - DAB对感觉动作电位幅度的影响不明确。这些发现支持了1,2 - 二乙酰苯衍生物的形成导致1,2 - DEB神经毒性的假设。