NAD+ and nicotinamide: sex differences in cerebral ischemia

Neuroscience. 2013 May 1:237:223-31. doi: 10.1016/j.neuroscience.2013.01.068. Epub 2013 Feb 9.

Abstract

Background: Previous literature suggests that cell death pathways activated after cerebral ischemia differ between the sexes. While caspase-dependent mechanisms predominate in the female brain, caspase-independent cell death induced by the activation of poly(ADP-ribose) polymerase (PARP) predominates in the male brain. PARP-1 gene deletion decreases infarction volume in the male brain, but paradoxically increases damage in PARP-1 knockout females.

Purpose: This study examined stroke-induced changes in NAD+, a key energy molecule involved in PARP-1 activation in both sexes.

Methods: Mice were subjected to middle cerebral artery occlusion and NAD+ levels were assessed. Caspase-3 activity and nuclear translocation were assessed 6h after ischemia. In additional cohorts, Nicotinamide (500 mg/kg i.p.) a precursor of NAD+ or vehicle was administered and infarction volume was measured 24h after ischemia.

Results: Males have higher baseline NAD+ levels than females. Significant stroke-induced NAD+ depletion occurred in males and ovariectomized females but not in intact females. PARP-1 deletion prevented the stroke-induced loss in NAD+ in males, but worsened NAD+ loss in PARP-1 deficient females. Preventing NAD+ loss with nicotinamide reduced infarct in wild-type males and PARP-1 knockout mice of both sexes, with no effect in WT females. Caspase-3 activity was significantly increased in PARP-1 knockout females compared to males and wild-type females, this was reversed with nicotinamide.

Conclusions: Sex differences exist in baseline and stroke-induced NAD+ levels. Nicotinamide protected males and PARP knockout mice, but had minimal effects in the wild-type female brain. This may be secondary to differences in energy metabolism between the sexes.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Analysis of Variance
  • Animals
  • Brain Ischemia / metabolism*
  • Caspase 3 / metabolism
  • Disease Models, Animal
  • Female
  • Male
  • Mice
  • Mice, Knockout
  • NAD / metabolism*
  • Niacinamide / metabolism*
  • Ovariectomy
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases / deficiency
  • Poly(ADP-ribose) Polymerases / genetics
  • Poly(ADP-ribose) Polymerases / metabolism
  • Sex Characteristics*
  • Spectrin / metabolism
  • Subcellular Fractions / enzymology

Substances

  • NAD
  • Spectrin
  • Niacinamide
  • Parp1 protein, mouse
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases
  • Caspase 3