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. 2002 Jul;51(1):113–119. doi: 10.1136/gut.51.1.113

Table 2.

Effect of the inhibitors of PKC, PKA, and Ca2+ dependent signalling pathways used in this study on cVA of CLF

Control BAPTA/AM H7 SP KT5720
cVA of CLF (%) 61 (7) 57 (3) 56 (7) 55 (3) 58 (10)

Hepatocyte couplets were incubated for 30 minutes at 37°C with DMSO (control), BAPTA/AM, H7, SP, or KT5720, before adding CLF and assessing cVA of CLF, as described in the methods section.

All values are mean (SD); n= 4–6 separated set of couplet preparations.

Differences between groups were not statistically significant.

CLF, cholyl-lysyl-fluorescein; BAPTA/AM, 1,2-bis-(o-aminophenoxy) -ethene-N,N,N`,N`-tetra-acetate tetra-(acetomethyl)ester; DMSO, dimethyl sulphoxide; cVA, canalicular vacuolar accumulation; PKA, protein kinase A; PKC, protein kinase C; SP, staurosporine.