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. 2005 Jun 24;5:12. doi: 10.1186/1471-2210-5-12

Table 1.

Effects of Diltiazem (50 μg/ml), Actinomycin D (1 μg/ml), EGTA (1 mM), KCl (100 mM), and BABTA/AM (16 μg/ml) on AA Release from HT-29 or C-9 Cells stimulated by TET or THAP.

Some biological effects* Agent tested Action of test agent AA Release
HT-29 C-9
TET Diltiazem Blocks L-type Ca2+ channels NI NI
Ion Channels Actinomycin D Inhibits RNA synthesis NI NI
Apoptosis EGTA Chelates extracellular Ca2+ NI NI
Depolarization 100 mM KCl Depolarizes NI NI
[Ca2+]I BAPTA/AM Chelates [Ca2+]i NI **

THAP Diltiazem Blocks L-type Ca2+ channels NI NI
Ion Channels Actinomycin D Inhibits RNA synthesis
Apoptosis EGTA Chelates extracellular Ca2+
Depolarization 100 mM KCl Depolarizes
[Ca2+]i BAPTA/AM Chelates [Ca2+]I **

* = References in text

NI = No Inhibition (or stimulation)

↓ = Inhibition: statistically significant

** = BAPTA/AM (16 μg/ml) stimulates AA release (6.17 ± 0.088 (4)), MEM/BSA control vs (11.6 ± 0.322 (4)), BAPTA/AM (16 μg/ml). Thus, the effect of BAPTA/AM on C-9 cells is not recorded.