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General Medical Research Laboratory, Veterans Administration Center, Togus, Maine
The effect of thiamine deficiency on the in vivo oxidation of methylglyoxal-1,3-14C and methylglyoxal-2-14C to 14CO2 was studied in the rat. The rapidity with which the 14C label appeared in the expired CO2 favors the interpretation that methylglyoxal metabolism is not impaired in the thiamine-deficient rat. The appearance of 14C label in liver glycogen and urine keto acids also indicated that it rapidly entered the classical metabolic pathways. The data suggest a rapid transformation of methylglyoxal to pyruvate and entrance into the Krebs cycle.