Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR

J Neurosci Res. 2005 Jan;79(1-2):119-27. doi: 10.1002/jnr.20308.

Abstract

We report a novel ((13)C, (2)H) nuclear magnetic resonance (NMR) procedure to investigate lactate recycling through the monocarboxylate transporter of the plasma membrane of cells in culture. C6 glioma cells were incubated with [3-(13)C]lactate in Krebs-Henseleit Buffer containing 50% (2)H(2)O (vol/vol) for up to 30 hr. (13)C NMR analysis of aliquots progressively taken from the medium, showed: (1) a linearly decreasing singlet at approximately 20.85 parts per million (ppm; -0.119 micromol/mg protein/hr) derived from the methyl carbon of [3-(13)C]lactate; and (2) an exponentially increasing shifted singlet at approximately 20.74 ppm (0.227 micromol/ mg protein/hr) from the methyl carbon of [3-(13)C, 2-(2)H]lactate. The shifted singlet appears because during its transit through the cytosol, [3-(13)C]lactate generates [3-(13)C, 2-(2)H]lactate in the lactate dehydrogenase (LDH) equilibrium, which may return to the incubation medium through the reversible monocarboxylate carrier. The methyl group of [3-(13)C, 2-(2)H]lactate is shifted -0.11 ppm with respect to that of [3-(13)C]lactate, making it possible to distinguish between both molecules by (13)C NMR. During incubations with 2.5 mM [1-(13)C]glucose and 3.98 mM [U-(13)C(3)]lactate or with 2.5 mM [1-(13)C]glucose and 3.93 mM [2-(13)C]pyruvate, C2-deuterated lactate was produced only from [1-(13)C]glucose or [U-(13)C(3)]lactate, revealing that this deuteration process is redox sensitive. When [1-(13)C]glucose and [U-(13)C(3)]lactate were used as substrates, no significant [3-(13)C]lactate production from [1-(13)C]glucose was detected, suggesting that glycolytic lactate production may be stopped under the high lactate concentrations prevailing under mild hypoxic or ischemic episodes or during cerebral activation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon Isotopes / metabolism
  • Cell Line
  • Cell Membrane / metabolism*
  • Citric Acid Cycle / physiology
  • Glioma / metabolism
  • Glucose / metabolism
  • Isotopes / metabolism
  • L-Lactate Dehydrogenase / metabolism
  • Lactic Acid / metabolism*
  • Magnetic Resonance Spectroscopy
  • Mice
  • Pentose Phosphate Pathway / physiology*
  • Pyruvic Acid / metabolism
  • Substrate Cycling
  • Time Factors
  • Tromethamine / metabolism

Substances

  • Carbon Isotopes
  • Isotopes
  • Krebs-Henseleit solution
  • Tromethamine
  • Lactic Acid
  • Pyruvic Acid
  • L-Lactate Dehydrogenase
  • Glucose