Veldre I A, Jänes H J
Environ Health Perspect. 1979 Jun;30:141-6. doi: 10.1289/ehp.7930141.
Estonian shale oil contains about 25--30% phenols, and their action determines the toxicity of shale oils. The clinical symptoms of intoxication are rather similar, regardless of route of administration. Due to neurotropic action, the coordination of movements is impaired, and clonic and tetanic convulsions, paresis and paralysis of extremities, and narcosis are observed. In subacute and chronic toxicity tests, dysfunction of the central nervous system was found. In long-term (4--6 month) experiments, changes in liver and kidney function were found. Shale oil has gonadotropic activity and causes changes in the sexual cycle as well as diminution of the number of primordial folicles in the ovaries or a decrease in the quantity of normal spermatogonia in testicular germinal epithelium. Shale oils produce local irritation of skin and mucous membranes. Shale oil can induce sensitization of the organism after repeated administration. The results of acute intoxication tests have proved that volatile and nonvolatile phenol fractions, isomeric dimethylphenols, and 5-methylresorcinol, must be characterized as moderately toxic substances; the LD50 ranges from 501 to 1500 mg/kg. The clinical symptoms of acute toxication are similar for all studied phenols (restlessness, unsteadiness, clonic tremor, paresis and paralysis of extremities, and death). In spite of the moderate toxicity of phenols in acute experiments, repeated administration of small doses can cause different changes in the nervous system and internal organs of experimental animals. For all the phenols studied, the maximum allowable concentration in water was limited by their effect on the organoleptic properties of water. The nonactive dose for warm-blooded animals is from 100 to 3000 times the threshold limit value of phenols on the basis of their organoleptic properties. The effect of commercial products of oil shale industry is generally determined by the toxicity of the main components: water-soluble oil shale phenols.
爱沙尼亚页岩油含有约25%至30%的酚类物质,其作用决定了页岩油的毒性。无论给药途径如何,中毒的临床症状都相当相似。由于其对神经的作用,运动协调性受损,会出现阵挛性和强直性惊厥、肢体轻瘫和麻痹以及麻醉状态。在亚急性和慢性毒性试验中,发现中枢神经系统功能障碍。在长期(4至6个月)实验中,发现肝脏和肾脏功能发生变化。页岩油具有促性腺活性,会导致性周期改变,以及卵巢中原始卵泡数量减少或睾丸生精上皮中正常精原细胞数量减少。页岩油会对皮肤和黏膜产生局部刺激。反复给药后,页岩油可使机体致敏。急性中毒试验结果证明,挥发性和非挥发性酚类馏分、异构二甲基酚和5 - 甲基间苯二酚必须被归类为中等毒性物质;半数致死剂量范围为501至1500毫克/千克。所有研究的酚类物质急性中毒的临床症状相似(烦躁不安、不稳、阵挛性震颤、肢体轻瘫和麻痹以及死亡)。尽管在急性实验中酚类物质毒性中等,但小剂量反复给药会导致实验动物神经系统和内脏出现不同变化。对于所有研究的酚类物质,水中的最大允许浓度受其对水的感官性质的影响限制。基于其感官性质,温血动物的无作用剂量是酚类物质阈限值的100至3000倍。油页岩工业商业产品的影响通常由主要成分——水溶性油页岩酚的毒性决定。