A Study on Subchronic Inhalation Toxicity of Isoprene Using Sprague-Dawely Rats

Isoprene 아급성 흡입독성 연구

  • Chung, Yong Hyun (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute) ;
  • Lee, Sung Bae (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute) ;
  • Han, Jeong Hee (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute) ;
  • Kang, Min Gu (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute) ;
  • Kim, Jong Kyu (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute) ;
  • Rim, Kyung Taek (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute) ;
  • Yang, Jung Sun (Chemical Safety and Health Research Center, Occupational Safety & Health Research Institute)
  • 정용현 (산업안전보건연구원 화학물질안전보건센터) ;
  • 이성배 (산업안전보건연구원 화학물질안전보건센터) ;
  • 한정희 (산업안전보건연구원 화학물질안전보건센터) ;
  • 강민구 (산업안전보건연구원 화학물질안전보건센터) ;
  • 김종규 (산업안전보건연구원 화학물질안전보건센터) ;
  • 임경택 (산업안전보건연구원 화학물질안전보건센터) ;
  • 양정선 (산업안전보건연구원 화학물질안전보건센터)
  • Received : 2011.03.28
  • Accepted : 2011.05.30
  • Published : 2011.06.30

Abstract

The purpose of this study was to obtain scientific information regarding classification and health hazards that may result from a 13 weeks inhalation exposure of isoprene in Sprague-Dawley (SD) rats. The testing method was conducted in accordance with OECD guidelines for the testing of chemicals No. 413. The Rats were divided into 4 groups (10 male and 10 female rats in each group) and exposed to 0, 360, 1,620, 7,300 ppm isoprene in each exposure chamber for 6 h/day, 5 days/week, for 13 weeks. As a result, there were no mortality or abnormality during the period of study and did not show any significant changes of body weight. There were no dose response changes in urinalysis, hematological and serum biochemical value examination. Relative organ weight was increased significantly the right kidney in 7,300 ppm group of male rats. In female rats, relative organ weight of the left kidney and the both lungs in 1,620 ppm group and the left lung and the both kidneys in 7,300 ppm group were increased significantly. But the histopathological findings did not reveal any exposure-related changes. According to the above results, the no observable adverse effect level (NOAEL) of isoprene was 7,300 ppm (20.3 mg/L) in both male and female rats. In conclusion, Isoprene was not classified specific target organ toxicity of the 'Standard for Classification and Labeling of Chemical Substance and Material Safety Data Sheet' (Ministry of Employment and Labor, 2009).

Keywords

References

  1. 노동부고시 제2009-68호 "화학물질의 분류.표시 및 물질안전보건자료에 관한 기준" 2009.
  2. Affek HP, Yakir D, Protection by isoprene against singlet oxygen in leaves, Plant Physiol 2002;129:269-277 https://doi.org/10.1104/pp.010909
  3. Karl, T, Prazeller, P, Mayr, D, Jordan, A, Rieder, J, Fall, R, Lindinger, W, Human breath isoprene and its relation to blood cholesterol levels; new measurements and modeling, J Appl Physiol 2001;91:762-770 https://doi.org/10.1152/jappl.2001.91.2.762
  4. Kuzuyama T, Seto H, Diversity of the biosynthesis of the isoprene units, Nat Prod Rep 2003;20:171-183 https://doi.org/10.1039/b109860h
  5. Hurst HE, Toxicology of 1,3-butadiene, Chloroprene, and Isoprene. Reviews of environmental contamination and Toxicology 2007;189:131-179
  6. Melnick RL, Sills RC, Comparative carcinogenicity of 1,3- butadiene, isoprene, and chloroprene in rats and mice. Chem-Biol Interact 2001;135-136:27-42 https://doi.org/10.1016/S0009-2797(01)00213-7
  7. Melnick RL, Sills RC, Roycroft JH, Chou BJ, Ragan HA, Miller RA, Isoprene, and endogenous hydrocarbon and industrial chemical, induces multiple organ neoplasia in rodents after 26 wees of inhalation exposure. Cancer Res 1994;54:5333-5339
  8. NTP, NTP toxicology and carcinogenesis studies of isoprene in F344/N rats (inhalation studies). Natl Toxicol Program Tech Rep Ser 1999;486:1-176
  9. NTP, Isoprene CAS No. 78-79-5. U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program, Research Triangle Park, NC. 2005c.
  10. OECD, OECD guideline for Testing of chemicals: 413 Subchronic Inhalation Toxicity: 90-day study, 2009.
  11. IARC, Isoprene, IARC Monographs on the Evaluation of Carcinogenic Risks to Humans 1999c; vol 71, pt 3, 1015-1025
  12. Placke ME, Griffis L, Bird M, Bus J, Persing RL, Cox LA Jr, Chronic inhalaton oncogenicity study of isoprene in B6C3F mice. Toxicology 1996; 113:253-262 https://doi.org/10.1016/0300-483X(96)03454-3
  13. Sharkey TD, Isoprene synthesis by plants and animals, Endeavour 1996;20:74-78 https://doi.org/10.1016/0160-9327(96)10014-4
  14. Watson WP, Cottrell L, Zhang D, Golding BT, Metabolism and molecular toxicology of isoprene, Chem-Biol Interact 2001;135-136:223-238 https://doi.org/10.1016/S0009-2797(01)00192-2