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. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: Eur J Neurosci. 2010 Aug 16;32(6):894–904. doi: 10.1111/j.1460-9568.2010.07372.x

Table 1. NAD+ levels are reduced by SD and oxidant exposures, and are restored by pyruvate, nicotinamide, and TPEN.

Near-pure cortical neuronal cultures were exposed and total cellular NAD+ was isolated at the times indicated which are prior to neuronal death (n >10).

Condition NAD+ (nmols/mg) FBP (nmols/mg)
Control 2.9 ± 0.2 4.0 ± 0.3
  + Zn2+ preload 2.76 ± 0.2 N.P.
30 µM Ethacrynic acid (2 hr) 1.69 ± 0.15 * 11.3 ± 0.5 *
  + 10 mM pyruvate 2.27 ± 0.13 # 5.1 ± 0.3 #
  + 10 mM nicotinamide 2.35 ± 0.13 # 5.3 ± 0.4 #
  + Zn2+ preload 0.29 ± 0.03 # N.P.
80 µM H2O2 (2 hr) 0.69 ± 0.03 * 14.3 ± 0.6 *
  + 10 mM nicotinamide 2.64 ± 0.18 # 6.4 ± 0.8 #
  + 10 µM TPEN 1.82 ± 0.07 # 7.2 ± 0.7 #
  + Zn2+ preload 0.29 ± 0.03 # N.P.
Serum deprivation (6 hr) 2.01 ± 0.12 * 7.9 ± 0.3 *
  + 10 mM pyruvate 2.45 ± 0.04 # 5.0 ± 0.4 #
  + 10 mM nicotinamide 2.66 ± 0.05 # 5.2 ± 0.5 #
  + 10 µM TPEN 2.62 ± 0.2 # 6.2 ± 0.2 #
  + Zn2+ preload 1.39 ± 0.07 # N.P.
*

indicates a significant difference from control.

#

indicates a significant difference from toxin alone at P < 0.05 by one-way ANOVA followed by a Bonferroni test.