Abstract

1. 1. Isolated perfused livers from mice infected with Trypanosoma brucei rhodesiense formed substantially more [3- 13C]-lactate from [3- 13C]-alanine than livers from uninfected mice. Quantities formed by infected livers increased as infection progressed. 2. 2. Infected livers produced more 13C-labeled glutamate and glutamine, with label scrambled between C-2 and C-3. Scrambling also produced [2,3- 13C]-aspartate, [2- 13C]-alanine and [2- 13C]-lactate. Delayed appearance of label in C-4 of glutamate/glutamine in infected liver reflects significant endogenous stores of unlabeled acetyl CoA. 3. 3. Although differences do exist in catabolism of [3- 13C]-alanine by perfused livers from infected and control mice, trypanosomiasis does not cause permanent breakdown or blockage of hepatic alanine metabolism.

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