Evaluation of Potassium Bromate-induced Acute Toxicity by Clinical Pathological Parameters in Rats

  • Hwang, Seok-Youn (Department of Clinical Pathology, Chungbuk National University Hospital) ;
  • Kang, Eun-Kyung (Department of Food and Nutrition, Chungbuk National University Hospital) ;
  • Kyung, Jong-Su (Korea Ginseng and Tobacco Research Institute) ;
  • Kim, Ki-Nam (Department of Food and Nutrition, Chungbuk National University Hospital) ;
  • Lee, Kwang-Joo (Department of Clinical Pathology, Chungbuk National University Hospital) ;
  • Wee, Jae-Joon (Korea Ginseng and Tobacco Research Institute)
  • 발행 : 2001.12.01

초록

This studs was carried out to evaluate KBrO$_3$-induced acute toxicity by clinical pathological parameters in rats. Fourty rats were divided into 4 groups including normal group and three KBrO$_3$-treated groups with doses of 200, 300, and 400 mg/kg, p. o., respectively. Creatinine and BUN were increased remarkably by KBrO$_3$ at 400 mg/kg, respectively (p<0.05, p<0.01). Phosphorus content increased two times the control at 400 mg/kg (p<0.05). Osmolarity was increased, whereas $CO_2$ content showed decrease at 400 mg/kg, respectively (p<0.01, p<0.05). Histopathological findings also showed dose-dependent renal failure. On the other hand, AST was increased three times the control at 400 mg/kg (p<0.01). WBC was increased by KBrO$_3$ depending on the dosage. Platelet was decreased at 200 mg/kg, whereas it was increased at 400 mg/kg (p<0.05). The results above suggest that clinical pathological parameters could be used as indices for the evaluation of KBrO$_3$-induced acute toxic reponse occuring in not only kidney but other organs including liver, when the dosage is as high as 400 mg/kg.

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