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. 1997 Apr 15;94(8):4086–4091. doi: 10.1073/pnas.94.8.4086

Table 1.

DHR fluorescence in GT1-1 trk cells

Condition 10 min 40 min
+ NGF 8 ± 4 44 ± 5
− NGF 57 ± 5* 181 ± 9*
 + 100 μM Meclofenamate 30 ± 2 125 ± 6
 + 20 μM Rotenone 22 ± 6 94 ± 14
 NGF + 10 μM PD98059 19 ± 4 53 ± 4
 NGF + 50 μM PD98059 54 ± 6* 152 ± 7*
 NGF + 100 μM PD98059 68 ± 5* 179 ± 8*
No calcium
 + NGF 35 ± 4 86 ± 8
 − NGF 30 ± 5 84 ± 7

Free radical production in GT1-1 trk cells detected as increased fluorescence due to oxidation of DHR to rhodamine 123. Values represent the percent change in brightness from basal values obtained just after loading DHR 123. All drugs were added as a 30-min pretreatment by including the drug with the DHR loading solution. Solutions used for most experiments contained 1.8 mM calcium, whereas solutions for the low-calcium condition contained no added calcium but did not include a calcium chelator to drop the calcium concentration to 0. Values represent the mean ± SEM for n = 40–300 for each group. 

*

Versus +NGF condition. P < 0.05 by ANOVA followed by Student–Newman–Keuls. 

Versus −NGF condition. P < 0.05 by ANOVA followed by Student–Newman–Keuls.