An active component of Achyranthes bidentata polypeptides provides neuroprotection through inhibition of mitochondrial-dependent apoptotic pathway in cultured neurons and in animal models of cerebral ischemia

PLoS One. 2014 Oct 15;9(10):e109923. doi: 10.1371/journal.pone.0109923. eCollection 2014.

Abstract

An active component has been isolated by reverse-phase high performance liquid chromatography (HPLC) from Achyranthes bidentata Blume polypeptides that are extracted from Achyranthes bidentata Blume, a Chinese medicinal herb. The active component is called ABPPk based on the order of HPLC elution. In this study, we used in vitro and in vivo experimental models of cerebral ischemia to investigate the possible neuroprotective effect of ABPPk. ABPPk treatment promoted neuronal survival and inhibited neuronal apoptosis in primary cortical neurons exposed to oxygen and glucose deprivation and in rats subjected to transient middle cerebral artery occlusion. The role of ABPPk in protection against ischemia-induced neuronal damage might be mediated by mitochondrial-dependent pathways, including modulation of apoptosis-related gene expression, regulation of mitochondrial dysfunction through restoring mitochondrial membrane potential, reducing release of mitochondrial apoptogenic factors, and inhibiting intracellular ROS production. The neuroprotective effect of ABPPk may suggest the possible use of this agent in the treatment and prevention of cerebral ischemic stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Achyranthes*
  • Animals
  • Apoptosis / drug effects*
  • Brain Ischemia / drug therapy*
  • Brain Ischemia / metabolism
  • Brain Ischemia / pathology
  • Caspase 3 / metabolism
  • Cells, Cultured
  • Disease Models, Animal
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Neuroprotective Agents / pharmacology*
  • Neuroprotective Agents / therapeutic use
  • Plant Extracts / pharmacology*
  • Plant Extracts / therapeutic use
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • Neuroprotective Agents
  • Plant Extracts
  • Reactive Oxygen Species
  • Caspase 3

Grants and funding

This study was supported by National Key Basic Research Program of China (973 program, Grant No. 2014CB542202), Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), Nantong Science and Technology Innovation Project (Grant No. HS2013003), and the natural science research project of Nantong University (Grant No. 11Z035 and 13ZY009). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.