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. 2013 Sep 23;8(9):e74344. doi: 10.1371/journal.pone.0074344

Table 2. Effect of huprines pretreatment on NGF differentiated PC12 cells survival after exposure of cells to H2O2 (200 µM).

TREATMENT % PROTECTION 48 H
Huprine X (1 µM) 53±5.0*
Huprine X (0.1 µM) 44±6.0*
Huprine X (1 µM) +MEC (100 µM) 7±3.2b
Huprine X (1 µM) +ATR (0.1 µM) 32±2.7b
Huprine Y (1 µM) 56±5.0*
Huprine Y (0.1 µM) 49±6.1*
Huprine Y (1 µM) +MEC (100 µM) 2.3±0.9b
Huprine Y (1 µM) +ATR (0.1 µM) 16±1.6b
Huprine Z (1 µM) 56±7.0*
Huprine Z (0.1 µM) 47±7.5*
Huprine Z (1 µM) +MEC (100 µM) 17±3.4b
Huprine Z (1 µM) +ATR (0.1 µM) 27±7.1b

Effect of antagonists mecamylamine (MEC) and atropine (ATR) on huprines protective effect on PC12 cells survival after exposure of the cells to H2O2. See Methods for details of cell treatment and conditions. Values are expressed as percentage of protection (mean ± s.e.m.) obtained from at least three independent experiments run in triplicate. *P<0.05 as compared with H2O2–treated group; bP<0.05 as compared with 1 µM concentration of corresponding drug (Dunnett's test).