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. 2008 Sep 11;4(4):365–375. doi: 10.1007/s11302-008-9122-2

Table 1.

Effect of a P2Y1 receptor antagonist MRS2500, a P2 receptor antagonist suramin, a PKC inhibitor staurosporine, and depletion of extracellular Ca2+ on (a) 2-MeSADP- or (b) UDP-induced transient [Ca2+]i rise in the mouse islet and beta-TC6 cells

  +MRS2500 +Suramin +Staurosporine No extracellular Ca2+
  10 μM 30 μM 100 μM 1 μM
a
% of control (100 μM 2-MeSADP alone)
Mouse islet 49 ± 11 (n = 6)* 23 ± 8 (n = 5)* 15 ± 7 (n = 5)* 80 ± 13 (n = 3) 80 ± 11 (n = 7)
Beta-TC6 cells 35 ± 4 (n = 14)* 24 ± 3 (n = 16)* 49 ± 10 (n = 31)* 113 ± 11 (n = 24) 51 ± 12 (n = 30)*
b
% of control (200 μM UDP alone)
Mouse islet 11 ± 6 (n  = 4)* 120 ± 28 (n = 5) 112 ± 23 (n = 6)
Beta-TC6 cells 51 ± 6 (n = 15)* 82 ± 9 (n = 32) 65 ± 9 (n = 24)*

MRS2500 and suramin were added with the nucleotides simultaneously to the culture of the islet or to beta-TC6 cells in the presence of 5.5 mM glucose. The islet and beta-TC6 cells were preincubated with staurosporine for 20 min (mean ± SE)

*P < 0.05