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. 2011 Nov;28(3):435–450. doi: 10.1159/000335106

Table 1.

Tests of candidate inhibitors of pendrin-mediated 36Cl influx. % inhibition is presented in bold if statistically significant (p<0.05, one-way ANOVA), and in gray in parentheses if p>0.05.

Candidate Inhibitor n Concentration (mM) Mean 36C1 uptake (nmol h−1 ± SE) P-Value Inhibition(%)
Oocyte background (water-injected) 29 0.17 ±0.05
Without drug 24 15.6 ±1.37
DIDS, 20°C 14 0.5 18.70 ±5.49 ns (0)
DIDS, 37°C 8 0.5 14.72 ±10.16 ns (6)
DIDS, 20°C, chloride-free 15 0.5 14.75 ±6.81 ns (5)
DIDS, 37°C, chloride-free 8 0.5 19.65 ±14.53 ns (0)
Tenidap 19 0.1 7.92 ±1.23 <0.001 49
Niflumic acid 10 0.1 8.41 ±1.58 0.020 46
NS 3623 8 0.1 10.1 ±2.37 ns (35)
Hydrochlorothiazide 10 1 10.6 ±1.01 ns (32)
Flufenamic acid 10 0.1 11.9 ±2.05 ns (24)
PMA 10 0.01 12.1 ±2.18 ns (23)
a-Cyano-3-hydroxy-cinnamic acid 10 1 13.5 ±1.61 ns (13)
6-Ethoxy-2-Benzothiazolesulfenamide 10 0.1 14.1 ±1.76 ns (10)
Wortmannin 10 0.1 15.7 ±2.32 ns (0)
UK 5099 9 1 16.9 ±1.65 ns (0)
4-Hydroxy-cinnamic acid 6 1 19.6 ±3.35 ns (0)
Levamisole 9 1 21.0 ±2.08 ns (0)
Trans-cinnamic acid 9 1 22.1 ±1.55 ns (0)