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British Journal of Industrial Medicine logoLink to British Journal of Industrial Medicine
. 1983 May;40(2):199–203. doi: 10.1136/oem.40.2.199

An experimental study of the combined effects of n-hexane and methyl ethyl ketone.

Y Takeuchi, Y Ono, N Hisanaga, M Iwata, M Aoyama, J Kitoh, Y Sugiura
PMCID: PMC1009172  PMID: 6830718

Abstract

This study was intended to determine whether or not methyl ethyl ketone (MEK) enhances the neurotoxicity of n-hexane at low concentration and after long term exposure. Separate groups of eight rats were exposed to 100 ppm n-hexane, 200 ppm MEK, 100 ppm n-hexane plus 200 ppm MEK, or fresh air in an exposure chamber for 12 hours a day for 24 weeks. The body weight, motor nerve conduction velocity (MCV), distal motor latency (DL), and mixed nerve conduction velocities (MNCVs) were measured before exposure and after four, eight, 12, 16, 20, and 24 weeks' exposure. One rat of each group was histopathologically examined after 24 weeks' exposure. Exposure of 100 ppm n-hexane did not significantly decrease the functions of the peripheral nerve throughout the experiment. Exposure to 200 ppm MEK significantly increased MCV and MNCVs and decreased DL after four weeks' exposure, but at this later stage no significant changes were found throughout the experiment by comparison with the controls. Mixed exposure to 100 ppm n-hexane plus 200 ppm MEK significantly decreased by comparison with the controls. On histopathological examination of the tail nerve, however, no changes were found in any of the exposed groups or the controls. These results suggest that MEK might enhance the neurotoxicity of n-hexane at a low concentration, and mixed exposures to n-hexane and MEK should be avoided.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abdel-Rahman M. S., Hetland L. B., Couri D. Toxicity and metabolism of methyl n-butyl ketone. Am Ind Hyg Assoc J. 1976 Feb;37(2):95–102. doi: 10.1080/0002889768507418. [DOI] [PubMed] [Google Scholar]
  2. Allen N., Mendell J. R., Billmaier D. J., Fontaine R. E., O'Neill J. Toxic polyneuropathy due to methyl n-butyl ketone. An industrial outbreak. Arch Neurol. 1975 Apr;32(4):209–218. doi: 10.1001/archneur.1975.00490460025001. [DOI] [PubMed] [Google Scholar]
  3. Altenkirch H., Mager J. Toxische Polyneuropathien durch Schnüffeln vn Pattex-Verdünner. Dtsch Med Wochenschr. 1976 Feb 6;101(6):195–199. doi: 10.1055/s-0028-1104059. [DOI] [PubMed] [Google Scholar]
  4. Altenkirch H., Stoltenburg G., Wagner H. M. Experimental studies on hydrocarbon neuropathies induced by methyl-ethyl-ketone (MEK). J Neurol. 1978 Dec 7;219(3):159–170. doi: 10.1007/BF00314531. [DOI] [PubMed] [Google Scholar]
  5. Billmaier D., Allen N., Craft B., Williams N., Epstein S., Fontaine R. Peripheral neuropathy in a coated fabrics plant. J Occup Med. 1974 Oct;16(10):665–671. [PubMed] [Google Scholar]
  6. Couri D., Abdel-Rahman M. S., Hetland L. B. Biotransformation of n-hexane and methyl n-butyl ketone in guinea pigs and mice. Am Ind Hyg Assoc J. 1978 Apr;39(4):295–300. doi: 10.1080/0002889778507761. [DOI] [PubMed] [Google Scholar]
  7. Ono Y., Takeuchi Y., Hisanaga N., Iwata M., Kitoh J., Sugiura Y. Neurotoxicity of petroleum benzine compared with n-hexane. Int Arch Occup Environ Health. 1982;50(3):219–229. doi: 10.1007/BF00378084. [DOI] [PubMed] [Google Scholar]
  8. Ono Y., Takeuchi Y., Hisanaga N. [Studies on the method of measuring nerve conduction velocity in rat's tail and on the comparative toxicity of n-hexane, methyl n-butyl ketone and 5,5-hexanedione (author's transl)]. Sangyo Igaku. 1979 Nov;21(6):528–538. doi: 10.1539/joh1959.21.528. [DOI] [PubMed] [Google Scholar]
  9. Saida K., Mendell J. R., Weiss H. S. Peripheral nerve changes induced by methyl n-butyl ketone and potentiation by methyl ethyl ketone. J Neuropathol Exp Neurol. 1976 May;35(3):207–225. doi: 10.1097/00005072-197605000-00001. [DOI] [PubMed] [Google Scholar]
  10. Sanagi S., Seki Y., Sugimoto K., Hirata M. Peripheral nervous system functions of workers exposed to n-hexane at a low level. Int Arch Occup Environ Health. 1980;47(1):69–79. doi: 10.1007/BF00378330. [DOI] [PubMed] [Google Scholar]
  11. Spencer P. S., Schaumburg H. H., Sabri M. I., Veronesi B. The enlarging view of hexacarbon neurotoxicity. Crit Rev Toxicol. 1980 Oct;7(4):279–356. doi: 10.3109/10408448009037489. [DOI] [PubMed] [Google Scholar]
  12. Takeuchi Y., Hisanaga N., Ono Y., Inoue T. [Toxicity and dose-response (effect) relationship of n-hexane (author's transl)]. Sangyo Igaku. 1980 Nov;22(6):470–487. doi: 10.1539/joh1959.22.470. [DOI] [PubMed] [Google Scholar]
  13. Takeuchi Y., Ono Y., Hisanaga N. An experimental study on the combined effects of n-hexane and toluene on the peripheral nerve of the rat. Br J Ind Med. 1981 Feb;38(1):14–19. doi: 10.1136/oem.38.1.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Takeuchi Y., Ono Y., Hisanaga N., Kitoh J., Sugiura Y. A comparative study on the neurotoxicity of n-pentane, n-hexane, and n-heptane in the rat. Br J Ind Med. 1980 Aug;37(3):241–247. doi: 10.1136/oem.37.3.241. [DOI] [PMC free article] [PubMed] [Google Scholar]

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