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. 1997 Sep 2;94(18):9962–9966. doi: 10.1073/pnas.94.18.9962

Table 2.

Summary of the effects of PMA on 8cpt-cAMP-induced responses in EBV-transformed lymphocytes

Basal, nS 8cpt-cAMP, nS 8cpt-cAMP + PMA, nS
Wild-type
 Absence of chelerythrine 0.40 ± 0.14 (12) 1.42 ± 0.59 (12) 0.38 ± 0.16* (9)
 With chelerythrine 0.32 ± 0.20 (4) 1.33 ± 0.41 (4) 1.10 ± 0.44 (4)
Heterozygous (overall, 24) 0.46 ± 0.14 3.03 ± 1.38 1.99 ± 1.65*
 Wild-type-like (5) 0.51 ± 0.18 1.42 ± 0.38 0.54 ± 0.19*
 “Intermediate” (14) 0.44 ± 0.13 2.93 ± 0.78 1.51 ± 0.64*
 Homozygous-like (5) 0.47 ± 0.07 4.92 ± 1.06 4.79 ± 1.04
Homozygous (16) 0.52 ± 0.17 4.71 ± 1.28 4.60 ± 1.27

In the wild-type group, the presence of chelerythrine in the pipet solution significantly reduced the inhibition by PMA (P < 0.001) but had no effect on either the basal conductance or the response to 8cpt-cAMP. The values obtained for PMA are significantly different from the slope conductance values obtained with 8cpt-cyclic AMP alone with the exception of the homozygous-like and homozygous variant: ∗, P < 0.05. 8cpt-cAMP was applied intracellularly via the recording pipet.