Effect of Coexposure to Methyl Ethyl Ketone (MEK) onn-Hexane Toxicokinetics in Human Volunteers

• Published in: Toxicology and applied pharmacology 1997-06, Vol.144 (2), p.385-395
• Main Authors: van Engelen, Jacqueline G.M., Rebel-de Haan, Wilhelmina, Opdam, Joannes J.G., Mulder, Gerard J.
• Format: Article
• Language: English
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1006/taap.1997.8149

In order to study the effects of methyl ethyl ketone (MEK) on the toxicokinetics ofn-hexane and, in particular, the formation of 2,5-hexanedione fromn-hexane in humans, volunteers were exposed ton-hexane (approx. 60 ppm, 2.4 μmin the inhaled air) with or without simultaneous inhalatory coexposure to MEK for 15.5 min. The concentration–time course ofn-hexane (in exhaled alveolar air) and its neurotoxic metabolite, 2,5-hexanedione (in serum), were studied. The concentration–time courses obtained after exposure ton-hexane alone were compared with those obtained after coexposure to 200 or 300 ppm MEK in the same volunteer on the same day. No effect of MEK was observed on the concentration–time course of exhaledn-hexane. The concentration–time course of the metabolite, 2,5-hexanedione, revealed a decrease in the rate of formation of 2,5-hexanedione (about threefold) after coexposure to MEK. Furthermore, the time to reach the peak concentration was increased from 18 to 30 min after the start of exposure. These changes in the concentration–time course of 2,5-hexanedione caused by MEK are most likely the result of inhibition of the biotransformation of one of the intermediate steps in the conversion ofn-hexane to 2,5-hexanedione. These results indicate that the interaction ofn-hexane and MEK leads to a decreased concentration of the neurotoxic metabolite 2,5-hexanedione (after short-term, acute exposure).