Conjugation of acetaldehyde with cysteinylglycine, the first metabolite in glutathione breakdown byγ-glutamyltranspeptidase
- Cite this article as:
- Kera, Y., Kiriyama, T. & Komura, S. Agents and Actions (1985) 17: 48. doi:10.1007/BF01966681
- 101 Downloads
Glutathione and its metabolites were examined for reactivity to acetaldehyde. When acetaldehyde was incubated with glutathione alone, there was only a slight decrease of acetaldehyde, while an apparently equimolar reaction between acetaldehyde and free sulfhydryl was observed with the addition of γ-glutamyltranspeptidase. Cysteinylglycine, the first metabolite in the glutathione breakdown by γ-glutamyltranspeptidase, showed a rapid and equimolar reactivity to acetaldehyde and such was comparable to the reaction seen withl-cysteine ord-penicillamine. In light of the chemical structure, cysteinylglycine probably conjugates with acetaldehyde to form thiazolidinecarboxylic acid derivatives, 2-methyl-thiazolidine-4-carbonyl-glycine, and if so, the alteration of glutathione metabolism by acetaldehyde during ethanol intoxication warrants further attention.