Proportional activities of glycerol kinase and glycerol 3-phosphate dehydrogenase in rat hepatomas

Biochem J. 1975 Jun;148(3):545-50. doi: 10.1042/bj1480545.

Abstract

The activities of glycerol 3-phosphate dehydrogenase (EC 1.1.1.8), glycerol kinase (EC 2.7.1.30), lactate dehydrogenase (EC 1.1.1.27), "malic' enzyme (L-malate-NADP+ oxidoreductase; EC 1.1.1.40) and the beta-oxoacyl-(acyl-carrier protein) reductase component of the fatty acid synthetase complex were measured in nine hepatoma lines (8 in rats, 1 in mouse) and in the livers of host animals. With the single exception of Morris hepatoma 16, which had unusually high glycerol 3-phosphate dehydrogenase activity, the activities of glycerol 3-phosphate dehydrogenase and glycerol kinase were highly correlated in normal livers and hepatomas (r = 0.97; P less than 0.01). The activities of these two enzymes were not strongly correlated with the activities of any of the other three enzymes. The primary function of hepatic glycerol 3-phosphate dehydrogenase appears to be in gluconeogenesis from glycerol.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carcinoma, Hepatocellular / enzymology*
  • Cell Line
  • Fatty Acid Synthases / metabolism
  • Glycerol Kinase / metabolism*
  • Glycerolphosphate Dehydrogenase / metabolism*
  • Kinetics
  • L-Lactate Dehydrogenase / metabolism
  • Liver / enzymology
  • Liver Neoplasms / enzymology*
  • Neoplasms, Experimental / enzymology
  • Phosphotransferases / metabolism*
  • Rats

Substances

  • Glycerolphosphate Dehydrogenase
  • L-Lactate Dehydrogenase
  • Fatty Acid Synthases
  • Phosphotransferases
  • Glycerol Kinase