Institoris L, Papp A, Siroki O, Banerjee B D
Department of Public Health, Faculty of Medicine, University of Szeged, Dom ter 10, H-6720 Szeged, Hungary.
Ecotoxicol Environ Saf. 2004 Mar;57(3):270-7. doi: 10.1016/S0147-6513(03)00101-5.
The effects of 6 weeks of oral exposure to propoxur (PR; at doses of 0.851 and 8.51 mg/kg body wt.), methylparathion (MP; at doses of 0.218 and 0.872 mg/kg body wt.), and their combinations were investigated in male Wistar rats. Measurement endpoints of the investigation were certain general toxicological parameters (body weight gain, organ weights), plaque-forming cell (PFC) count from the spleen, open field (OF) behavior, auditory startle response (ASR), prepulse inhibition (PPI), rotarod performance, somatosensory and auditory cortical evoked potentials, and peripheral nerve conduction velocity. The treated rats did not show any sign of acute intoxication during the 6 weeks of exposure. The higher dose of PR, but not of MP, significantly decreased the relative liver weight. Both agents produced a significant dose-dependent increase of OF activity, with larger expression after 2 weeks than after 6 weeks. The number of ASR responses and the ASR amplitude increased. The amplitude after PPI was increased by MP but only minimally altered by PR and the combinations. There was a small, but with high-dose PR significant, increase in the latency of the somatosensory evoked potentials. Neither of the two substances alone had any effect on the PFC response. The effect of the combination of high-dose PR and low-dose MP was significantly different from that of high-dose PR alone on the liver weight, on the ASR amplitude, and on the PFC/10(6) cell and PFC/spleen counts. With high-dose MP and low-dose PR, no such interaction was observed. According to the results, the noneffective dose of MP can influence the toxicity of the effective dose of PR in a combined exposure situation.
在雄性Wistar大鼠中研究了口服6周残杀威(PR;剂量为0.851和8.51毫克/千克体重)、甲基对硫磷(MP;剂量为0.218和0.872毫克/千克体重)及其组合的影响。研究的测量终点包括某些一般毒理学参数(体重增加、器官重量)、脾脏的空斑形成细胞(PFC)计数、旷场(OF)行为、听觉惊吓反应(ASR)、前脉冲抑制(PPI)、转棒性能、体感和听觉皮层诱发电位以及外周神经传导速度。在6周的暴露期间,处理过的大鼠未表现出任何急性中毒迹象。较高剂量的PR而非MP显著降低了相对肝脏重量。两种药剂均使OF活动显著剂量依赖性增加,2周后的表达比6周后的更大。ASR反应的数量和ASR幅度增加。MP增加了PPI后的幅度,但PR及其组合仅使其略有改变。体感诱发电位的潜伏期有小幅增加,但高剂量PR使其显著增加。两种物质单独使用均对PFC反应无任何影响。高剂量PR和低剂量MP组合对肝脏重量、ASR幅度以及PFC/10(6)细胞和PFC/脾脏计数的影响与单独高剂量PR的影响显著不同。高剂量MP和低剂量PR组合未观察到此类相互作用。根据结果,在联合暴露情况下,MP无效剂量可影响PR有效剂量的毒性。