目的探讨R,S和R/S型3-氯-1,2-丙二醇(3-MCPD)对ICR小鼠的急性毒性。方法选用健康性成熟ICR小鼠,对R,S及R/S型3-MCPD染毒剂量依次为176.78、198.43、222.73、250、280.61、314.98和353.55、396.84、445.44和499.99mg/kg,89.09,100,112.25,125.99,141.42,158.74和178.18mg/kg及130.25、150、172.75、198.95、229.13、263.88和303.91mg/kg。经口一次灌胃染毒观察14天,以改良寇式法计算LD50,计算脏体比并进行肝肾病理学检查。结果R,S及R/S型3-MCPD的LD50及95%可信区间(95%CI)分别为290.54mg/kg(280.74~300.68),117.57mg/kg(113.82,121.45),190.73mg/kg(177.76~204.59)。R型异构体在250mg/kg及以上剂量组动物肾体比显著增加(P〈0.05),脑体比在353.55mg/kg、445.44mg/kg及最高剂量组亦显著增大(P〈0.05);S型3-MCPD染毒组动物各脏体比与对照组比均无显著差异;R/S型3-MCPD,在198.95mg/kg及以上荆量组动物肾体比明显增加,在229.13mg/kg及以上剂量动物脑体比亦明显增加,与对照组比有差异显著(P〈0.05)。在353.55mg/kg及以上剂量R型异构体引起肝细胞肿胀、肝窦扩张和明显充血,在229.13mg/kg及以上荆量(R/S)型3-MCPD也引起肝细胞肿胀和肝窦充血,S型则未引起。R、S及(R,S)型均未引起肾脏明显的病理改变。结论三种3-MCPD急性毒性大小依次为S型〉R/S型〉R型,R、S型异构体均显示出神经毒性。
Objective To investigate the acute toxicity of R,S and (R,S) -3-monchloropropane-1,2-diol(3-MCPD). Methods 10,7 and 7 groups of sexually mature ICR mice were employed for testing the acute toxicity of R, S and (R, S)-3-MCPD, at the doses of 176.78,198.43,222.73,250,280.61,314.98 and 353.55mg/kg 396.84mg/kg, 445.44mg/ kg,499.99mg/kg for R-3-MCPD, 89.09,100,112.25,125.99,141.42,158.74 and 178.18mg/kg for S-3-MCPD and 130.25,150,172.75,198.95,229.13,263.88 and 303.91 mg/kg for ( R, S)-3- MCPD, respectively. The mice were given three forms of 3-MCPD once by gavage and observed for 14 days, the lethal dose 50s(LD50) were calculated by the modified Karber's method, organ/body weight ratios were measured and morphological changes of liver and kidney were examined. Results The LD50 (95% Cl)of R, S and (R,S)-3-MCPD were 290.54mg/kg(280.74 - 300.68), 117.57mg/ kg ( 113.82 - 121.45 ) and 190.73mg/kg( 177.76,204.59), respectively. The kidney/weight ratios in R-3- MCPD treated groups were higher than controls at the doses of 250 - 353.55mg/kg (P 〈 0.05), and the brain weight ratios also had an significant increase in the 353.55mg/kg,445.44mg/kg and above doses (P 〈 0.05 ). However, no significant change on organ/body weight ratio of any organs in S-3-MCPD treated groups were observed. The kidney/body weight ratio in (R, S)- 3-MCPD treated groups increased significantly at the doses of 198.95 - 303.91mg/kg( P 〈 0.05), and the brain weight ratios also had a significant increase at the doses of 229.13~ 303.91mg/kg. At the doses of 353.55 ~ 499.99mg/kg, R-3- MCPD caused obvious swell of liver cells and the swell and congestion of the liver sinus. At the dose 229.13mg/kg and above, (R, S)-3-MCPD also induced the swell of liver cells and congestion of the liver sinus. No obvious morphological changes of kidney after administration of R, S and (R, S)-3-MCPD were observed. Conclusion The results indicated that the acute toxicity of S-3-MCPD may be much higher