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Hydrogen sulfide promotes proliferation and neuronal differentiation of neural stem cells and protects hypoxia-induced decrease in hippocampal neurogenesis.

Abstract
Accumulating evidence has suggested that hydrogen sulfide (H2S) acts as a novel neuro-modulator and neuroprotective agent; however, it remains to be investigated whether H2S has a direct effect on neural stem cells (NSCs). In the present study, we examined the effects of H2S donor, sodium hydrosulfide (NaHS) on mouse NSCs and hippocampal neurogenesis. We report here that NaHS promoted proliferation and neuronal differentiation of NSCs. Further analysis revealed that NaHS-induced proliferation was associated with phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 and neuronal differentiation was linked to altered expression of differentiation-related genes. In addition, C57BL/6 mice (1 day old) subjected to hypoxia were treated with NaHS to explore whether H2S would influence the neurogenesis of hippocampus. BrdU incorporation assay results showed that administration of NaHS could increase the number of proliferating cells in the dentate gyrus of hippocampus in the mice after hypoxia. Moreover, Morris water maze test showed that treatment with NaHS improved cognitive impairment after hypoxia in mice. These findings suggest that H2S may afford a novel therapeutic strategy to intervene in the progression of brain diseases.
AuthorsDexiang Liu, Zhen Wang, Jingmin Zhan, Qun Zhang, Jianmei Wang, Qingrui Zhang, Xiuying Xian, Qinsong Luan, Aijun Hao
JournalPharmacology, biochemistry, and behavior (Pharmacol Biochem Behav) Vol. 116 Pg. 55-63 (Jan 2014) ISSN: 1873-5177 [Electronic] United States
PMID24246910 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Elsevier Inc. All rights reserved.
Chemical References
  • DNA Primers
  • Hydrogen Sulfide
Topics
  • Animals
  • Base Sequence
  • Cell Differentiation (drug effects)
  • Cell Proliferation (drug effects)
  • DNA Primers
  • Hippocampus (drug effects, pathology)
  • Hydrogen Sulfide (pharmacology)
  • Hypoxia (pathology)
  • MAP Kinase Signaling System
  • Mice
  • Mice, Inbred C57BL
  • Neural Stem Cells (cytology, drug effects)
  • Neurogenesis (drug effects)
  • Phosphorylation
  • Polymerase Chain Reaction
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction

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