The excretion and biotransformation of rac-alpha -lipoic acid (LA), which i
s used for the symptomatic treatment of diabetic polyneuropathy, were inves
tigated following single oral dosing of [C-14]LA to mice (30 mg/kg), rats (
30 mg/kg), dogs (10 mg/kg), and unlabeled LA to humans (600 mg). More than
80% of the radioactivity given was renally excreted, Metabolite profiles ob
tained by radiometric high-performance liquid chromatography revealed that
LA was extensively metabolized irrespective of the species, Based on a new
on-line liquid chromatography/tandem mass spectroscopy assay developed for
negative ions, LA and a total of 12 metabolites were identified. Mitochondr
ial beta -oxidation played the paramount role in the metabolism of LA, Simu
ltaneously, the circulating metabolites were subjected to reduction of the
1,2-dithiolane ring and subsequent S-methylation. In addition, evidence is
given for the first time that the methyl sulfides formed were partly oxidiz
ed to give sulfoxides, predominantly in dogs, The disulfoxide of 2,4-bismet
hylmercapto-butanoic acid, the most polar metabolite identified, was the ma
jor metabolite in dogs, Furthermore, new data are presented that suggest co
njugation with glycine occurred as a separate metabolic pathway in competit
ion with P-oxidation, predominantly in mice.