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. Author manuscript; available in PMC: 2012 Sep 23.
Published in final edited form as: Biochem Pharmacol. 2005 Apr 15;69(8):1215–1223. doi: 10.1016/j.bcp.2005.01.018

Table 1.

Effect of uracil derivatives or P2 receptors antagonists on cardiomyocytes subjected to hypoxia

Treatment LDH release (%)
Normoxia 4.2 ± 0.6
Hyp 40 ± 2.4
Hyp + UTP 10 ± 1.6*
Hyp + uridine 29 ± 2.5
Hyp + UDP 36 ± 2.6
Hyp + 5-HD 37 ± 0.6
Hyp + UTP + 5-HD 12 ± 1.6*
Hyp + UTP + PPADS 32 ± 3.6
Hyp + UTP + suramin 25 ± 3.5
Hyp + UTP + RB-2 11 ± 0.8*

Cardiomyocytes were treated with 50 μM uridine, UDP, or UTP or with P2 receptor antagonist PPADS (10 μM), RB-2 (50 μM), or suramin (300 μM) or with 5-HD, a mitochondrial KATP channel inhibitor (300 μM), for 15 min before hypoxia. The cells were then washed twice and subjected to hypoxia for 2 h in glucose-free PBS, at 37 °C. The amount of LDH released to the medium was determined and compared to the total activity of control homogenate (100%). Data are means of at least three replicates in three separate experiments ± S.D.

*

P < 0.01 compared with hypoxia.