N.Formation of the structure of an organism or part differentition and growth of tissues and organs during development
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[14C]Oxalate was found in the urine of fasted male Wistar rats fed l-[14C3]-serine, dl-[14V2]serine, [14C1]ethanolamine, [14C1]hydroxypyruvate, [14C3]hydroxypyruvate, [14C1]glycolate or [14C2]glyxylate, [14C1]Hydroxypyrusvate and [14C1]ethanolamine were the least effective precursors of [14C]oxalate. 20% of the [14C1]serine and [14C3]serine administered was recovered as 14CO2, while less then 4% was metabolized by pathways known to contribute to oxalate synthesis. Oxalate synthesis from serine involved both the transamination to hydroxypyruvate and the conversion to glycine, but not decarboxylation to ethanolamine. The oxidation of [14C2]glyoxylate to [14C]oxlate inhibited by hydroxypyruvate, but the oxidation of [14C1]glycolate to [14C]oxlate was not significantly altered. [14C]Glycolaldehyde, [14C]glycolate, [14C]glyoxylate and [14C]oxalate were recovered in the urine of rats administratered [14C3]hydroxypyruvate. This is consistent with the oxidation of hydroxypyruvate via glycolaldehyde → glycolate → glyoxylate → oxalate and is identical to the metabolic pathway for the oxidation of ethylene glycol to oxalate. However, the major metabolic intermediate recovered from [14C3]hydroxypyruvate was [14C]glyoxylate rather than [14C]glycolate, suggesting that an laternate pathway is contributing to the oxidation of hydroxypyruvate to oxalate in the rat.
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