Effects of salvianolic acid B on survival, self-renewal and neuronal differentiation of bone marrow derived neural stem cells

Eur J Pharmacol. 2012 Dec 15;697(1-3):32-9. doi: 10.1016/j.ejphar.2012.10.008. Epub 2012 Oct 18.

Abstract

Our previous study has demonstrated the therapeutic potential of bone marrow derived-neural stem cells (BM-NSCs) in CNS disorders; however, the beneficial effects are modest due to the poor survival and low neural differentiation frequency. Here, we demonstrate that salvianolic acid B (Sal B), a potent aqueous of a well known Chinese medicine herb, Salvia miltiorrhiza, possesses the ability to promote BM-NSCs proliferation in a dose dependent manner as verified by growth curve and Bromodeoxyuridine (BrdU) incorporation assays; While in differentiation medium, Sal B promoted nestin(+) BM-NSCs differentiated into greater numbers of NF-M(+) neurons and NG2(+) oligodendrocyte precursors, but fewer GFAP(+) astrocytes as verified by triple immunostaining and quantitative analysis; upon exposure to H(2)O(2), Sal B facilitated the cells survival, reduced LDH leakage, and inhibited apoptosis, displaying a dose-dependent neuroprotective effect on BM-NSCs. Sal B induced brain-derived neurotrophic factor (BDNF) production by BM-NSCs, which may be beneficial for the cells survival and differentiation in unfavourable environment. The collective evidence indicates that Sal B may be a potential drug to upgrade the therapeutic efficiency of BM-NSCs in CNS diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Antigens / metabolism
  • Apoptosis / drug effects
  • Benzofurans / pharmacology*
  • Biomarkers / metabolism
  • Bone Marrow Cells / drug effects*
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / pathology
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cell Proliferation / drug effects*
  • Cell Survival / drug effects
  • Cytoprotection
  • Dose-Response Relationship, Drug
  • Glial Fibrillary Acidic Protein
  • Hydrogen Peroxide / toxicity
  • Immunohistochemistry
  • L-Lactate Dehydrogenase / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / metabolism
  • Neural Stem Cells / drug effects*
  • Neural Stem Cells / metabolism
  • Neural Stem Cells / pathology
  • Neurofilament Proteins / metabolism
  • Neurogenesis / drug effects*
  • Neuroprotective Agents / pharmacology*
  • Oxidants / toxicity
  • Phenotype
  • Proteoglycans / metabolism
  • Spheroids, Cellular
  • Time Factors

Substances

  • Antigens
  • Benzofurans
  • Biomarkers
  • Brain-Derived Neurotrophic Factor
  • Glial Fibrillary Acidic Protein
  • Nerve Tissue Proteins
  • Neurofilament Proteins
  • Neuroprotective Agents
  • Oxidants
  • Proteoglycans
  • chondroitin sulfate proteoglycan 4
  • glial fibrillary astrocytic protein, mouse
  • neurofilament protein M
  • Hydrogen Peroxide
  • salvianolic acid B
  • L-Lactate Dehydrogenase