Luty S, Latuszynska J, Obuchowska-Przebirowska D, Tokarska M, Haratym-Maj A
Department of Pathomorphology, Institute of Agricultural Medicine, P.O.Box 185, 20-950 Lublin, Poland.
Ann Agric Environ Med. 2000;7(1):33-41.
The effect of a synthetic pyrethroid - alpha-cypermethrin administered per os for 28 days to Swiss mice was examined on phagocytic and bactericidal activity of neutrophils, and leukocytic image, IL-12 p70 level in blood plasma, as well as histologic and ultrastructural picture of the liver, heart, kidneys, lung and spleen. A synthetic pyrethroid alpha-cypermethrin, [(R,S)-alpha-cyano-3-phenoxybenzyl (R,S)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate], produced by the Chemical Plant in Jaworzno was used in the study. The preparation for the application per os was used in doses 1/2 LD(50) (25 mg/kg body mass) and 1/5 LD(50) (10 mg/kg body mass). The results were presented as mean (x) +/- standard error (SEM) and subjected to statistical analysis by the parametric t-Student test. Subacute poisoning of mice with alpha-cypermethrin in doses 1/2 LD(50) and 1/5 LD(50) resulted in decreased bactericidal activity of neutrophils. The dose 10 mg/kg body mass had a stronger stimulatory effect on phagocytic activity than 25 mg/kg body mass. Significantly higher numbers of monocytes and lymphocytes were observed in the blood of male mice poisoned with 1/5 LD(50) alpha-cypermethrin. The administration of alpha-cypermethrin resulted for both doses in the decrease in IL-12 p70 serum secretion. The lowest IL-12 p70 level (pg/ml) was noted among female mice administered 1/2 LD(50) of the preparation. The results of the study may indicate that the pyrethroid in the study had a suppressive effect on Il-12 p70 production. In mice administered 1/5 LD(50) or 1/2 LD(50) of the preparation examined, histopathologic and ultrastructural changes were observed in the liver and kidneys.
研究了将合成拟除虫菊酯 - α - 氯氰菊酯经口给予瑞士小鼠28天,对中性粒细胞的吞噬和杀菌活性、白细胞图像、血浆中IL - 12 p70水平以及肝脏、心脏、肾脏、肺和脾脏的组织学和超微结构图像的影响。本研究使用了由 Jaworzno 的化工厂生产的合成拟除虫菊酯α - 氯氰菊酯,即[(R,S)-α - 氰基 - 3 - 苯氧基苄基 (R,S)-顺,反 - 3 - (2,2 - 二氯乙烯基)-2,2 - 二甲基环丙烷羧酸酯]。经口给药制剂的使用剂量为1/2 LD(50)(25毫克/千克体重)和1/5 LD(50)(10毫克/千克体重)。结果以平均值(x)±标准误差(SEM)表示,并通过参数t检验进行统计分析。用1/2 LD(50)和1/5 LD(50)剂量的α - 氯氰菊酯对小鼠进行亚急性中毒,导致中性粒细胞杀菌活性降低。10毫克/千克体重的剂量对吞噬活性的刺激作用比25毫克/千克体重更强。在经1/5 LD(50)α - 氯氰菊酯中毒的雄性小鼠血液中观察到单核细胞和淋巴细胞数量显著增加。两种剂量的α - 氯氰菊酯给药均导致IL - 12 p70血清分泌减少。在给予1/2 LD(50)制剂的雌性小鼠中观察到最低的IL - 12 p70水平(皮克/毫升)。研究结果可能表明,该研究中的拟除虫菊酯对Il - 12 p70的产生有抑制作用。在给予1/5 LD(50)或1/2 LD(50)受试制剂的小鼠中,在肝脏和肾脏中观察到组织病理学和超微结构变化。