INHIBITION OF THE GLYCOLYTIC PATHWAY BY METHYLGLYOXAL IN HUMAN-PLATELETS
INHIBITION OF THE GLYCOLYTIC PATHWAY BY METHYLGLYOXAL IN HUMAN-PLATELETS
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DOI:
10.1002/cbf.290070111
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发表时间:
1989-01-01
影响因子:
3.6
通讯作者:
BUZZI, E
中科院分区:
文献类型:
--
作者:
LEONCINI, G;MARESCA, M;BUZZI, E
The incubation of human platelets with methylglyoxal and glucose produces a rapid transformation of the ketoaldehyde to D-lactate by the glyoxalase system and a partial reduction in GSH. Glucose utilization is affected at the level of the glycoltytic pathway. No effect of the ketoaldehyde on glycogenolysis and glucose oxidation through the hexose monophosphate shunt was demonstrated. Phosphofructokinase, fructose 1,6 diphosphate (F1, 6DP) aldolase, glyceraldehyde 3-phosphate dehydrogenase and 3-phosphoglycerate mutase wree mostly inhibited by methylglyoxal. A decrease in lactate and pyruvate formation and an accumulation of some glycolytic intermediates (fructose 1,6 diphosphate, dihydroxyacetone phosphate, 3-phosphoglycerate) was observed. Moreover methylglyoxal induced a fall in the metabolic ATP concentration. Since methlglyoxal is an intermediate of the glycolytic bypase system form dihydroxyacetone phosphate to D-lactate, it may be assumed that ketoaldehyde exerts a rgulating effect on triose metabolism.