首页> 外文期刊>Kurume Medical Journal >EXPERIMENTAL STUDIES ON THE TOXICITY OF BENZENE HEXACHLORIDE (BHC) AND DICHLORODIPHENYLTRICHLOROETHANE (DDT)I. TOXICITY TESTS OF THE INSECTICIDES FOLLOWING VARIOUS ADMINISTRATIONS TO LABORATORY ANIMALS
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EXPERIMENTAL STUDIES ON THE TOXICITY OF BENZENE HEXACHLORIDE (BHC) AND DICHLORODIPHENYLTRICHLOROETHANE (DDT)I. TOXICITY TESTS OF THE INSECTICIDES FOLLOWING VARIOUS ADMINISTRATIONS TO LABORATORY ANIMALS

机译:苯六甲醚(BHC)和二氯二苯甲酰间苯三酚(DDT)毒性的实验研究I.对实验室动物进行各种管理后,杀虫剂的毒性测试

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The summary of the above-mentioned experiments are as follows: 1) In the acute toxicity test, as shown in Table 13, the lethal doses in various administrations, though considerable differences can be seen according to the kinds of laboratory animals or their degrees of growth, are the lowest in gamma BHC, next the BHC-mixture and the highest DDT. It is shown that DDT is less toxic than BHC. As for gamma BHC, in the case of intraperitoneal injection, the lethal dose is the least; in subcutaneous injection, peroral administration and percutaneous administration, in that order the lethal doses increase. This proves that in the intraperitoneal injection the absorption is the fastest. Subcutaneous injection and peroral administration are next to it and in percutaneous administration, absorption is the slowest. On the contrary, in the case of DDT, the aspects are a little different. In peroral administration the absorption is the fastest, and the absorption decreases in the following order, i. e., intraperitoneal injection, percutaneous administration and subcutaneous injection. These variations in the lethal doses seem to be due to the irregularities of absorption of each oil solution and the differences of the antidotal action of the liver and the other organs. Moreover, the kind of solvents and the methods of administration may be concerned with the velocity of absorption or with the antidotal action. Comparing the time required to express toxic symptoms in each oil solution, as shown in Table 14, BHC is faster than DDT in cases of intraperitoneal and subcutaneous injections, and DDT is faster than BHC in peroral and percutaneous administrations. In addition, comparing the time required to die in each administration, as shown in Table 14, in gamma BHC intraperitoneal injection requires the least time and decreases in the following order : subcutaneous injection, peroral and percutaneous administrations. In DDT, peroral administration requires the least time and decreases in the following order : intraperitoneal, percutaneous and subcutaneous administrations. The amount of time required to die coincides with the strength of toxicity in the lethal dose of acute toxicity in Table 13. Next to summarized the toxic symptoms in each oil solution, less than the lethal dose of BHC resulted in loss of appetite and excitability were seen, but the growth of animals was not prevented. As for the symptoms caused by a greater than lethal dose, respiration is at first hastened then a calmness could be seen. After several minutes or several hours later, excitability rose to madness, hemorrhages could be seen at nasal passages, around eye-lids and from the vaginal opening of female rats. Tremors were barely noticed, though some died after convulsions. Some survived after the convulsions and were growing naturally. In pregnant rats the toxic symptoms were severe and the lethal dose was lower. On these symptoms, Cameron, Slade, Létard & deSacy, Tareeva recognized almost the same results. In DDT, compared with BHC, the symptoms are revealed remarkably well, that is, tremors easily appeared with less than lethal dose there was a sensitiveness to outer stimuli, especially to sounds. There was also a momentary reaction of jumping and more remarkable tremors were observed when these stimuli came. Some recovered gradually from tremors and showed normal growth afterwards. Others could not take food because of tremors gradually becoming violent, laid down laterally . The limbs became paralyzed and most of them died shortly thereafter. The remarkable loss of weight was possibly caused by this impossibility to take food or loss of appetite. Besides the hemorrhages, which could be seen in the case of BHC poisoning, at nasal part, around eye-lids and from the vaginal opening of female rats, were not entirely observed.
机译:上述实验总结如下:1)在急性毒性试验中,如表13所示,尽管根据实验动物的种类或它们的受精程度,可以看到相当大的差异,但各种给药中的致死剂量。增长幅度最小的是γBHC,其次是BHC混合物,而DDT最高。结果表明,滴滴涕的毒性小于六六六。至于γBHC,在腹腔注射的情况下,致死剂量最小;在皮下注射,经口给药和经皮给药中,致死剂量依次增加。这证明在腹膜内注射中吸收最快。其次是皮下注射和经口给药,在经皮给药中吸收最慢。相反,就DDT而言,方面有所不同。在经口给药中,吸收是最快的,并且吸收按以下顺序降低,即。例如,腹膜内注射,经皮给药和皮下注射。致死剂量的这些变化似乎是由于每种油溶液吸收的不规则性以及肝脏和其他器官的解毒作用的差异所致。此外,溶剂的种类和给药方法可能与吸收速度或解毒作用有关。如表14所示,比较在每种油溶液中表达毒性症状所需的时间,在腹膜内和皮下注射的情况下,BHC比DDT快,而在经口和经皮给药中,DDT比BHC快。另外,比较每次给药所需的死亡时间,如表14所示,在γBHC腹膜内注射中所需的时间最少,并且以以下顺序减少:皮下注射,经口和经皮给药。在DDT中,经口给药所需的时间最少,并且按以下顺序减少:腹膜内,经皮和皮下给药。死亡所需的时间与表13所示的急性毒性致死剂量的毒性强度相吻合。接下来总结每种油溶液的毒性症状,少于致死剂量的BHC导致食欲不振和兴奋性降低。看到了,但是动物的生长并没有被阻止。至于由大于致命剂量引起的症状,首先要加快呼吸,然后才能看到平静。几分钟或几小时后,兴奋性上升到疯狂,在鼻道,眼睑周围和雌性大鼠的阴道口可见出血。震颤几乎没有引起注意,尽管有些在抽搐后死亡。惊厥后一些幸存者得以自然生长。在怀孕的大鼠中,毒性症状很严重,致死剂量较低。在这些症状上,Cameron,Slade,Létard和deSacy,Tareeva认识到几乎相同的结果。在DDT中,与BHC相比,症状显着好,也就是说,在少于致死剂量的情况下容易出现震颤,对外部刺激(特别是对声音)敏感。当这些刺激来临时,还会有跳跃的瞬间反应,并观察到更明显的震颤。有些从震颤中逐渐恢复,然后恢复正常。其他人无法吃东西,因为震颤逐渐向侧面蔓延开来。肢体瘫痪,此后大部分人死亡。体重的显着下降可能是由于无法进食或食欲不振造成的。除了出血,在BHC中毒的情况下,在鼻部,眼睑周围和雌性大鼠的阴道开口处均未观察到出血。

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