Table 2. Cytotoxicity and proliferation of cells treated with JO146.
| Koala PBMC LDH Assay - % cytotoxicity (n = 4)α | |
| 100 μM JO146§ | DMSO |
| −3.10 ± (3.41) | 1.77 ± (3.02) |
| Koala PBMC MTS Assay - % proliferation (n = 4)α | |
| 100 μM JO146 | DMSO |
| 19.74 ± (3.041) | 0.29 ± (1.23) |
| Koala Uterine Tissue LDH Assay - % cytotoxicity (n = 2)α | |
| 100 μM JO146§ | DMSO§ |
| −3.96 ± (3.56) | −8.70 ± (6.17) |
| Koala Uterine Tissue MTS Assay - % proliferation (n = 2)α | |
| 100 μM JO146 | DMSO |
| 23.62 ± (0.20) | 10.54 ± (1.52) |
| Koala Conjunctival Tissue LDH Assay - % cytotoxicity (n = 1)α | |
| 100 μM JO146§ | DMSO |
| −10.76 | −18.69 |
| Koala Conjunctival Tissue MTS Assay - % proliferation (n = 1)α | |
| 100 μM JO146 | DMSO |
| 3.86 | 1.03 |
αExperiments were performed in triplicate and the results expressed as percentage cell death compared with untreated control cells by using the formula [1 − (mean absorbance of treated cells/mean absorbance of untreated cells)] * 100. Results are shown with SEM indicated in parenthesis.
§Negative values indicate treated cultures had less cytotoxicity/more proliferation than control.