• DOI:10.1152/AJPREGU.2000.279.1.R9
• Corpus ID: 5742970

Critical oxygen tension in rat brain: a combined (31)P-NMR and EPR oximetry study.

@article{Rolett2000CriticalOT,
  title={Critical oxygen tension in rat brain: a combined (31)P-NMR and EPR oximetry study.},
  author={Ellis L. Rolett and Ali Azzawi and K. J. Liu and Martin Yongbi and Harold M. Swartz and Jeff F. Dunn},
  journal={American journal of physiology. Regulatory, integrative and comparative physiology},
  year={2000},
  volume={279 1},
  pages={
          R9-R16
        }
}

• E. Rolett, A. Azzawi, +3 authors J. Dunn
• Published 1 July 2000
• Biology
• American journal of physiology. Regulatory, integrative and comparative physiology

The relationship between cerebral interstitial oxygen tension (Pt(O(2))) and cellular energetics was investigated in mechanically ventilated, anesthetized rats during progressive acute hypoxia to determine whether there is a "critical" brain Pt(O(2)) for maintaining steady-state aerobic metabolism. Cerebral Pt(O(2)), measured by electron paramagnetic resonance oximetry, decreased proportionately to inspired oxygen fraction. (31)P-nuclear magnetic resonance measurements revealed no changes in P(i), phosphocreatine (PCr)/P(i) ratio, or intracellular pH when arterial blood oxygen tension (Pa(O(2))) was reduced from 145.1 +/- 11.7 to 56.5 +/- 4.4 mmHg (means +/- SE). Intracellular acidosis, a sharp rise in P(i), and a decline in the PCr/P(i) ratio developed when Pa(O(2)) was reduced further to 40.7 +/- 2.3 mmHg. The corresponding Pt(O(2)) values were 15.1 +/- 1.8, 8.8 +/- 0.4, and 6.8 +/- 0.3 mmHg. We conclude that over a range of decreasing oxygen tensions, cerebral oxidative metabolism is not sensitive to oxygen concentration. Oxygen becomes a regulatory substrate, however, when Pt(O(2)) is decreased to a critical level.