Scorpion venom heat-resistant peptide (SVHRP) enhances neurogenesis and neurite outgrowth of immature neurons in adult mice by up-regulating brain-derived neurotrophic factor (BDNF)

PLoS One. 2014 Oct 9;9(10):e109977. doi: 10.1371/journal.pone.0109977. eCollection 2014.

Abstract

Scorpion venom heat-resistant peptide (SVHRP) is a component purified from Buthus martensii Karsch scorpion venom. Although scorpions and their venom have been used in Traditional Chinese Medicine (TCM) to treat chronic neurological disorders, the underlying mechanisms of these treatments remain unknown. We applied SVHRP in vitro and in vivo to understand its effects on the neurogenesis and maturation of adult immature neurons and explore associated molecular mechanisms. SVHRP administration increased the number of 5-bromo-2'-dexoxyuridine (BrdU)-positive cells, BrdU-positive/neuron-specific nuclear protein (NeuN)-positive neurons, and polysialylated-neural cell adhesion molecule (PSA-NCAM)-positive immature neurons in the subventricular zone (SVZ) and subgranular zone (SGZ) of hippocampus. Furthermore immature neurons incubated with SVHRP-pretreated astrocyte-conditioned medium exhibited significantly increased neurite length compared with those incubated with normal astrocyte-conditioned medium. This neurotrophic effect was further confirmed in vivo by detecting an increased average single area and whole area of immature neurons in the SGZ, SVZ and olfactory bulb (OB) in the adult mouse brain. In contrast to normal astrocyte-conditioned medium, higher concentrations of brain-derived neurotrophic factor (BDNF) but not nerve growth factor (NGF) or glial cell line-derived neurotrophic factor (GDNF) was detected in the conditioned medium of SVHRP-pretreated astrocytes, and blocking BDNF using anti-BDNF antibodies eliminated these SVHRP-dependent neurotrophic effects. In SVHRP treated mouse brain, more glial fibrillary acidic protein (GFAP)-positive cells were detected. Furthermore, immunohistochemistry revealed increased numbers of GFAP/BDNF double-positive cells, which agrees with the observed changes in the culture system. This paper describes novel effects of scorpion venom-originated peptide on the stem cells and suggests the potential therapeutic values of SVHRP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / drug effects
  • Brain-Derived Neurotrophic Factor / antagonists & inhibitors
  • Brain-Derived Neurotrophic Factor / biosynthesis*
  • Cell Proliferation
  • Culture Media, Conditioned / chemistry
  • Gene Expression Regulation, Developmental / drug effects
  • Glial Fibrillary Acidic Protein
  • Humans
  • Mice
  • Nerve Tissue Proteins / antagonists & inhibitors
  • Nerve Tissue Proteins / biosynthesis*
  • Neurites / drug effects
  • Neurogenesis / drug effects*
  • Neurons / drug effects
  • Peptides / administration & dosage*
  • Scorpion Venoms / administration & dosage*

Substances

  • Brain-Derived Neurotrophic Factor
  • Culture Media, Conditioned
  • Glial Fibrillary Acidic Protein
  • Nerve Tissue Proteins
  • Peptides
  • Scorpion Venoms
  • glial fibrillary astrocytic protein, mouse
  • scorpion venom heat-resistant peptide, Buthus martensii

Grants and funding

The work was supported by the National Natural Science Foundation of China (NO 81371223 and 81371437, http://www.nsfc.gov.cn), the Research Fund for the Doctoral Program of Higher Education of China (20122105110010, http://www.cutech.edu.cn/cn/kyjj/gdxxbsdkyjj/A010301index_1.htm) and Liaoning Province Science and Technology Plan Projects (2011226006, http://www.lninfo.gov.cn). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.