Table 1.
Tat-mediated increase in neuronal excitability is Tat specific and long lastinga
Cells with multiple APs/N | Em (mV) | Rheobase (pA) | AP threshold (mV) | AP height | |
---|---|---|---|---|---|
Control | 6/19 | −50.6 ± 1.5 | 20 ± 5 | −11.5 ± 2.7 | 77.7 ± 5.8 |
100 nm Tat | 19/20* | −49.2 ± 1.2 | 10 ± 2* | −16.1 ± 1.2* | 87.9 ± 3.8* |
Inactivated 100 nm Tat | 1/5 | −50.2 ± 1.4 | 20 ± 6 | −13.2 ± 1.4 | 71.7 ± 8.7 |
Tat− | 1/10 | −48.9 ± 4.6 | 24 ± 3 | −16.3 ± 1.3 | 51.9 ± 3.7 |
Tat+ | 11/11* | −52.5 ± 1.0 | 10 ± 0* | −21.0 ± 0.8* | 71.8 ± 2.4* |
aWhole-cell patch-clamp experiments in current-clamp mode on neurons pretreated with 100 nm Tat for 17 to 48 h. These neurons fired a statistically significant higher number of multiple action potentials and at lower rheobase and action potential thresholds compared with controls. Neurons treated with heat-inactivated Tat were less excitable compared with Tat pretreated and as excitable as controls (untreated neurons). Neurons isolated from Tat+ mice were also more excitable than Tat− mice neurons.
*p < 0.05 (paired t test).