Table 3.
Redox status of [NADH/[NAD+] in hypoxic nonreplicating Mtb H37Rv
| Drug treatment (μM) | NAD+, μM | NADH, μM | NADH/NAD+ ratio |
|---|---|---|---|
| No drug | 0.95 ± 0.11 | 0.3 ± 0.03 | 0.32 ± 0.01 |
| Thioridazine (40) | 0.72 ± 0.08 | 0.39 ± 0.04 | 0.54 ± 0.11* |
| Thioridazine (80) | 0.66 ± 0.04* | 0.56 ± 0.11* | 0.85 ± 0.22* |
| Rifampicin (1) | 0.90 ± 0.03 | 0.37 ± 0.03 | 0.41 ± 0.05 |
| R207910 (5) | 0.99 ± 0.03 | 0.38 ± 0.04 | 0.38 ± 0.05 |
| R207910 (10) | 1.16 ± 0.02 | 0.37 ± 0.02 | 0.31 ± 0.02 |
Hypoxic nonreplicating Mtb H37Rv was incubated with the ndh-2 inhibitor thioridazine for 3 h under anaerobic conditions before quantification of the [NADH]/[NAD+] ratio. The compounds were used at 2- and 4-fold of the WCC90 concentration for thioridazine and R207910 and at 2-fold the WCC90 concentration for rifampicin. The experiments were carried out three times in triplicate; one of the representative experiments is shown with means and standard deviations.
*Mean values are statistically different (P < 0.05) compared with the mean values of the no-drug-treated Mtb cells.