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. Author manuscript; available in PMC: 2009 Aug 15.
Published in final edited form as: Biochem Pharmacol. 2008 May 28;76(4):552–567. doi: 10.1016/j.bcp.2008.05.016

Table 1.

Effect of DCVC and mitochondrial inhibitors on ATP concentrations of hPT cells

Incubation ATP (% Control)
Control 100 ± 5.1
1 mM KCN + 0.1 mM Iodoacetate (KCN/IAA) [0.5 hr] 22.6 ± 7.3
1 μM Antimycin A (AA) 78.7 ± 3.3
1 μM Staurosporine (Sts) 78.7 ± 8.4
50 μM tert-Butyl hydroperoxide (tBH) 18.2 ± 2.1
DCVC:
   10 μM 80.0 ± 2.1
   50 μM 71.7 ± 3.9
   100 μM 60.7 ± 13.4
   200 μM 61.0 ± 8.0
   300 μM 48.3 ± 8.4

Primary cultures of hPT cells were grown to ∼80% confluence and then incubated with the indicated additions for 24 hr, except for KCN/IAA as noted. Cellular contents of ATP were determined by a luminescence assay and are expressed as the percent of control. Control = 8.63 nmol ATP/mg protein. Results are means ± SEM of measurements from 3 separate cell cultures, each derived from a different kidney. All values were significant different (P < 0.05) from those for Control cells.