Kim J S, Crichlow E C, Blakley B R, Rousseaux C G
Department of Veterinary Physiological Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Canada.
Vet Hum Toxicol. 1990 Apr;32(2):101-5.
The neurophysiological and histopathological alterations were evaluated in Sprague-Dawley rats exposed to 1,000 ppm lead in drinking water and treated with thiamin (25 mg/kg or 50 mg/kg bw), calcium ethylenediamine tetraacetic acid (CaEDTA) (50 mg/kg bw) or their combination for 8 weeks. Alterations in the brain-stem auditory evoked responses (BAERs) were observed during the treatment period. Latency periods associated with the BAERs were increased after 4 weeks of lead exposure. The neurophysiological alterations induced by lead exposure were prevented by thiamin or CaEDTA treatment. The latency periods in the lead exposed rats treated with thiamin, CaEDTA or the combined treatment did not increase in a similar fashion, but resembled more closely the latency periods observed in the rats which were not exposed to lead. The higher dose of thiamin (50 mg/kg) was more effective than the lower dose (25 mg/kg) in the comparable treatment groups. Histopathological examination of the animals did not reveal any pathological changes in the brain, although lesions often associated with lead toxicity were observed in the kidney. The severity of the lesions was not influenced by thiamin or CaEDta treatment. The absence of morphological damage in the CNS in the presence of neurophysiological alterations, indicates that functional deficits may be observed prior to histological evidence of pathological damage.
对饮用含1000 ppm铅的水并分别用硫胺素(25 mg/kg或50 mg/kg体重)、乙二胺四乙酸钙(CaEDTA)(50 mg/kg体重)或它们的组合进行处理8周的Sprague-Dawley大鼠的神经生理学和组织病理学改变进行了评估。在治疗期间观察到脑干听觉诱发电位(BAERs)的改变。铅暴露4周后,与BAERs相关的潜伏期延长。硫胺素或CaEDTA处理可预防铅暴露引起的神经生理学改变。用硫胺素、CaEDTA或联合处理的铅暴露大鼠的潜伏期没有以类似方式增加,而是更接近未暴露于铅的大鼠中观察到的潜伏期。在可比的治疗组中,较高剂量的硫胺素(50 mg/kg)比较低剂量(25 mg/kg)更有效。对动物的组织病理学检查未发现大脑有任何病理变化,尽管在肾脏中观察到了通常与铅毒性相关的病变。病变的严重程度不受硫胺素或CaEDta处理的影响。在存在神经生理学改变的情况下中枢神经系统没有形态学损伤,这表明在病理损伤的组织学证据出现之前可能观察到功能缺陷。