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. 2018 Oct 31;315(6):H1602–H1613. doi: 10.1152/ajpheart.00291.2018

Table 3.

Effect of DHEA and GDP-β-S on parameters of f-V and f-HP relationships

n V0.5, mV k, mV
Control, f-V 15 −30.3 (0.5) 7.5 (0.4)
30 µM DHEA 15 −36.2 (0.5)* 7.2 (0.5)
Control, f-HP 9~15 −41.8 (0.1) 6.0 (0.1)
10 µM DHEA 9~15 −43.4 (0.5)* 6.4 (0.4)
30 µM DHEA 9~15 −46.3 (0.5)* 6.3 (0.5)
100 µM DHEA 9~15 −52.4 (0.7)* 6.5 (0.9)
Control, f-V 15 −28.9 (0.5) 7.7 (0.4)
GDP-β-S, f-V 7 −23.1 (0.5)* 7.9 (0.4)

Mean (SD) values were obtained by fitting plot with 5 points for holding potential (HP)-dependent steady-state inactivation curves (f-HP) and 13 points for quasi-steady-state inactivation curves (f-V); n, number of cells. V0.5, voltage that causes a 50% reduction in the amplitude of the inactivating component of L-type Ca2+ current; k, slope factor. Statistical comparison in the absence and presence of dehydroepiandrosterone (DHEA) and control versus guanosine 5′-O-(2-thiodiphosphate) (GDP-β-S) was performed using ordinary one-way ANOVA followed by Dunnet’s test.

*

P < 0.001 compared with control.