Jodynis-Liebert Jadwiga, Bennasir Hassen A H
Department of Toxicology, Poznań University of Medical Sciences, Poznań, Poland.
Int J Toxicol. 2005 Sep-Oct;24(5):365-76. doi: 10.1080/10915810500210138.
The aim of the study was to investigate the effect of the dietary fat on selected parameters of toluidines toxicity in rats during subchronic exposure. Three isomers of toluidine (ortho, meta, and para) were administered to rats in the diet for 1 and 3 months at levels 40, 80, 160 mg/kg/day in two kinds of diet containing either 4% or 14% fat. All doses of toluidine isomers produced a 1.5- to 9.8-fold increase in methemoglobin (MetHb) level during both treatment periods. A distinct dose-response relationship was observed, especially for o- and m-toluidine; the effect was generally greater in rats fed high-fat diet. Reduced glutathione level in liver was increased in all treated groups, 1.5- to 5.1-fold, irrespective of the kind of diet. An increase in hepatic lipid peroxidation (thiobarbituric acid reactive substances; TBARS), 1.5- to 4.5-fold, was noticed in the majority of the treated groups. Generally, there was no consistent effect of diet except for p-toluidine where the level of hepatic TBARS was lower in rats fed high-fat diet. Blood urea nitrogen (BUN) level in animals treated with all doses of o- and m-toluidine was 1.3- to 5.0-fold higher in comparison with respective controls. No clear relationship between BUN level and the kind of diet was found. No effect of toluidines on the activity of serum aspartate aminotransferase (AST) and sorbitol dehydrogenase (SDH) were observed. In the majority of groups treated for 30 and 90 days the amount of toluidines in 24-h urine was lower in rats fed high-fat diet. Final body weight gain in rats treated with o- and p-toluidine (80 and 160 mg/kg body weight [b.w.]) was lower as compared to controls. In summary the high-fat diet stimulated methemoglobin formation in rats treated with o- and m-toluidine and cause the decrease in the amount of toluidines in 24-h urine. The high content of fat did not affect consistently the other parameters tested.
本研究的目的是调查亚慢性暴露期间饮食脂肪对大鼠甲苯胺毒性选定参数的影响。将三种甲苯胺异构体(邻位、间位和对位)以40、80、160mg/kg/天的剂量添加到两种分别含有4%或14%脂肪的饲料中,喂养大鼠1个月和3个月。在两个治疗期内,所有剂量的甲苯胺异构体均使高铁血红蛋白(MetHb)水平升高了1.5至9.8倍。观察到明显的剂量反应关系,尤其是邻位和间位甲苯胺;在高脂饮食喂养的大鼠中,这种影响通常更大。所有治疗组肝脏中还原型谷胱甘肽水平均升高,为1.5至5.1倍,与饮食种类无关。大多数治疗组肝脏脂质过氧化(硫代巴比妥酸反应性物质;TBARS)增加了1.5至4.5倍。一般来说,除了对位甲苯胺外,饮食没有一致的影响,在高脂饮食喂养的大鼠中,对位甲苯胺的肝脏TBARS水平较低。用所有剂量的邻位和间位甲苯胺处理的动物的血尿素氮(BUN)水平比各自的对照组高1.3至5.0倍。未发现BUN水平与饮食种类之间有明确关系。未观察到甲苯胺对血清天冬氨酸转氨酶(AST)和山梨醇脱氢酶(SDH)活性有影响。在大多数接受30天和90天治疗的组中,高脂饮食喂养的大鼠24小时尿液中的甲苯胺含量较低。用邻位和对位甲苯胺(80和160mg/kg体重[b.w.])处理的大鼠的最终体重增加低于对照组。总之,高脂饮食刺激了用邻位和间位甲苯胺处理的大鼠高铁血红蛋白的形成,并导致24小时尿液中甲苯胺含量降低。高脂肪含量并未始终影响所测试的其他参数。