Table 12. Nuclear Magnetic Resonance (31P-NMR)-Derived ATP Levels in Rat and Human Retinas under Normal and Hypoxic Conditions and Restoration of ATP with Two Different Drugsa.
experiments/treatments | ATP
and its phosphorus metabolites (% of control levels) |
||
---|---|---|---|
rat retinas | ATP | PCr | Pi |
normal controls | 98.4 ± 1.15 | 85.7 ± 2.3 | 95.0 ± 2.3 |
after 2.0 h hypoxia | 48.1 ± 2.1*** | nd | nd |
after 1.0 h hypoxia | 69.5 ± 3.46*** | 56.0 ± 4.6*** | 75.0 ± 8.6 |
after 1 h with MK-801 at 50 μM | 97.4 ± 4.6*** | 102.0 ± 4.5*** | 89.3 ± 4.04 |
after 2 h with MK-801 at 50 μM | 72.6 ± 1.4** | nd | nd |
after 1 h with MK-801 at 5 nM | 92.0 ± 1.4*** | 101.0 ± 5.7*** | 76.8 ± 3.57 |
human retinas | % of control ATP |
---|---|
normal controls | 98 ± 12 |
after 2.0 h hypoxia | 52 ± 8** |
after 2 h with MK-801 at 50 μM | 74 ± 6* |
after 2 h with diltiazem at 50 μM | 67 ± 4 |
Effect on tissue ATP and its metabolites after hypoxia/reperfusion of rat and human retinas in the absence and presence of MK-801 (NMDA-receptor-channel blocker) and diltiazem (Ca2+-channel blocker) as determined by 31P NMR spectroscopy. PCr = phosphocreatinin; Pi = inorganic phosphate; nd = not determined; *P < 0.05; **P < 0.02; ***P < 0.01. Data from ref (7).