Blockade of L-type voltage-gated Ca channel inhibits ischemia-induced neurogenesis by down-regulating iNOS expression in adult mouse

J Neurochem. 2005 Aug;94(4):1077-86. doi: 10.1111/j.1471-4159.2005.03262.x. Epub 2005 Jul 5.

Abstract

Neurogenesis in the adult mammalian hippocampus may contribute to repairing the brain after injury. The signals that regulate neurogenesis in the dentate gyrus following ischemic stroke insult are not well known. We have previously reported that inducible nitric oxide synthase (iNOS) expression is necessary for ischemia-stimulated neurogenesis in the adult dentate gyrus. Here, we show that mice subjected to 90 min of middle cerebral artery occlusion (MCAO) significantly increased the number of new neurons and up-regulated iNOS expression in the dentate gyrus. Blockade of the L-type voltage-gated Ca(2+) channel (L-VGCC) prevented neurogenesis in the dentate gyrus and subventricular zone (SVZ), and down-regulated iNOS expression in the dentate gyrus after cerebral ischemia. This study suggests that Ca(2+) influx through L-VGCC is involved in ischemia-induced neurogenesis by up-regulating iNOS expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arterial Occlusive Diseases / complications
  • Brain Ischemia / etiology
  • Brain Ischemia / physiopathology*
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels, L-Type / drug effects
  • Calcium Channels, L-Type / metabolism*
  • Cells, Cultured
  • Dentate Gyrus / physiopathology*
  • Diltiazem / pharmacology
  • Down-Regulation
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Cerebral Artery
  • Nerve Regeneration* / drug effects
  • Nimodipine / pharmacology
  • Nitric Oxide Synthase / metabolism*
  • Nitric Oxide Synthase Type II

Substances

  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Nimodipine
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Diltiazem