Table 1. Developmental sensitivity to bilirubin toxicity: the P8/P2 ratio of viability tests.
Hip | Cll | IC | SC | Ctx | |
---|---|---|---|---|---|
LDH | |||||
70 nM | 7.11 | 1.12 | 2.20 | 1.43 | 2.40 |
140 nM | 5.44c | 0.79 | 3.35b | 1.51 | 2.03 |
300 nM | 5.51c | 1.12 | 1.61 | 1.22 | 0.85 |
Hoechst | |||||
70 nM | 8.95b | 0.61 | 0.89 | 0.13 | 0.77 |
140 nM | 12.70c | 0.75 | 1.65 | 1.68 | 2.92 |
300 nM | 4.97c | 0.65 | 4.19c | 0.51 | 0.12 |
MTT | |||||
70 nM | 0.85 | 1.17 | 0.96 | 1.12 | 1.04 |
140 nM | 0.69 | 1.18 | 0.86 | 1.27 | 0.78 |
300 nM | 0.64 | 0.95 | 0.71 | 0.83 | 0.57 |
Lactate dehydrogenase release (LDH - upper), Hoechst staining of apoptotic bodies (middle) and mitochondrial activity (MTT - lower) were expressed as the ratio of P8 results divided by P2 results. A ratio greater than 1 demonstrates an increased sensitivity during the development for LDH and Hoechst data, the opposite for the MTT test. Statistical significance vs. DMSO ap < 0.05; bp < 0.01; cp < 0.001. Hip: hippocampus; Cll: cerebellum; IC: inferior colliculus; SC: superior colliculus; Ctx: cortex.