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. 2009 Feb 18;156(5):740–750. doi: 10.1111/j.1476-5381.2008.00072.x

Table 1.

The effects of NADA and NAGly on the kinetics of CaV3 channels

CaV channel Time to peak (ms)
Deactivation τ (ms)
Control NADA NAGly Control NADA NAGly
3.1 7.2 ± 0.3 6.2 ± 0.3 7.3 ± 0.3 3.2 ± 0.1 3.1 ± 0.1 3.2 ± 0.2
3.2 11.2 ± 0.4 11.5 ± 0.6 11.6 ± 0.4 3.1 ± 0.2 3.1 ± 0.2 3.1 ± 0.2
3.3 43 ± 1 44 ± 2 43 ± 2 2.4 ± 0.1 2.4 ± 0.2 2.3 ± 0.1

Cells expressing recombinant CaV3 channels were voltage clamped at −86 mV and then stepped to −26 mV. For examples of these experiments see Figures 2 and 3. The time to peak was measured directly and the decay of the current following repolarization of the membrane to −86 mV fit with a single exponential function. The concentration of NADA was 300 nmol·L−1 for CaV3.1 and CaV3.3 and 1 µmol·L−1 for CaV3.2. 10 µmol·L−1 NAGly was used for each channel. There were no differences in time to peak or deactivation for any current with either drug (paired t-test vs. predrug values for each cell). n = 6–8 for each condition.

NADA, N-arachidonoyl dopamine; NAGly, N-arachidonoyl glycine.