The potential role of nitric oxide synthase in survival and regeneration of magnocellular neurons of hypothalamo-neurohypophyseal system

Neurochem Res. 2009 Nov;34(11):1907-13. doi: 10.1007/s11064-009-9965-0. Epub 2009 Apr 21.

Abstract

Previous investigations from this laboratory have demonstrated that hypophysectomy induces up-regulation of neuronal nitric oxide synthase (nNOS) in magnocellular neurons of the mammalian hypothalamo-neurohypophyseal system (HNS). Accompanied by this upregulation of nNOS, both neuronal regeneration and degeneration are also observed in this system following hypophysectomy. The specific aim of this study was to determine the potential role of nNOS upregulation in neuronal survival and regeneration after hypophysectomy in the adult Sprague-Dawley (SD) rat by using a competitive nitric oxide synthase blocker, N(G)-nitrol-L: -arginine methyl ester (L: -NAME). We found that L: -NAME treatment effectively blocked the regeneration of magnocellular neurons of the rodent hypothalamus as observed in the lumen of the third cerebral ventricle following hypophysectomy. However, L: -NAME had no effect on the survival of magnocellular neurons in the supraoptic (SON) and paraventricular (PVN) nuclei after hypophysectomy. These results suggest that the induced increase of nNOS expression enhance the regenerative ability of magnocellular neurons of the HNS following hypophysectomy.

MeSH terms

  • Animals
  • Cell Survival
  • Hypophysectomy
  • Hypothalamo-Hypophyseal System / cytology*
  • Hypothalamo-Hypophyseal System / drug effects
  • Male
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Neuronal Plasticity
  • Neurons / cytology
  • Neurons / physiology*
  • Nitric Oxide Synthase Type I / antagonists & inhibitors
  • Nitric Oxide Synthase Type I / physiology*
  • Paraventricular Hypothalamic Nucleus / cytology
  • Paraventricular Hypothalamic Nucleus / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Regeneration
  • Supraoptic Nucleus / cytology
  • Supraoptic Nucleus / drug effects

Substances

  • Nitric Oxide Synthase Type I
  • NG-Nitroarginine Methyl Ester