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. 2001 Sep 1;535(Pt 2):519–532. doi: 10.1111/j.1469-7793.2001.00519.x

Table 1.

Effects of Ca2+ channel blockers on glucagon release

Condition 1 mM glucose 1mM glucose + 10 μM forskolin
Control 34.0 ± 2.6 (12) 100.5 ± 6.6 (12) *
1μM ω-conotoxin 18.8 ± 1.9 (10) * 92.1 ± 7.5 (10)
50 μM nifedipine 36.9 ± 4.1 (10) 55.5 ± 4.9 (10)

Glucagon release (pg islet−1 h−1) was measured following 1 h incubations in the presence of 1 mM glucose alone (left column) or following activation of adenylate cyclase with 10 μM forskolin (right column) in the presence of the L- and N-type Ca2+ channel blockers nifedipine and ω-conotoxin. Data are means ± S.E.M. of the indicated number of experiments (in parentheses).

*

P < 0.001vs. Control (1 mM glucose alone)

P < 0.001vs. glucagon release measured in 1 mM glucose + 10 μM forskolin.