[Neuroprotective effects and mechanism of ethanol extract of Cistanche tubulosa against oxygen-glucose deprivation/reperfusion]

Zhongguo Zhong Yao Za Zhi. 2019 Jul;44(13):2686-2690. doi: 10.19540/j.cnki.cjcmm.20181214.001.
[Article in Chinese]

Abstract

To investigate the inhibitory effects and mechanism of Cistanche tubulosa ethanol extract( CTEE) against oxygen-glucose deprivation/reperfusion( OGD/R)-induced PC12 cells neuronal injury. In this study,OGD/R-induced PC12 cells were used to explore the neuroprotective effects of CTEE( 12. 5,25,50 mg·L-1) by detecting cell viability with MTT assay,apoptosis with AO/EB and Hoechst 33258,mitochondrial membrane potential changes with JC-1 staining,mitochondrial oxidative stress with MitoSOX staining,as well as the apoptosis-related protein expression( PARP,cleaved PARP,caspase-3,cleaved caspase-3,Bax,Bcl-2) with Western blot. RESULTS:: showed that CTEE effectively protected OGD/R-induced neuronal injury and increased the survival rate of PC12 cells.AO/EB and Hoechst 33258 staining showed that CTEE could effectively inhibit apoptosis. Moreover,JC-1 and MitoSOX staining results showed that CTEE decreased mitochondrial stress and mitochondrial membrane potential imbalance in PC12 cells in a concentration-dependent manner. Meanwhile,CTEE could obviously suppress the activation of key proteins in mitochondrial apoptosis pathway such as caspase-3 and PARP,and significantly inhibit the rise of Bax and down-regulation of Bcl-2. In conclusion,CTEE has obvious protective effects on OGD/R-induced PC12 cells neuronal injury,potentially via inhibiting mitochondrial oxidative stress and apoptosis-related signaling pathway.

Keywords: Cistanche tubulosa; ethanol extract; mitochondri al pathway; neuronal injury; oxygen-glucose deprivation/reperfusion(OGD/R).

MeSH terms

  • Animals
  • Apoptosis*
  • Caspase 3 / metabolism
  • Cistanche / chemistry*
  • Ethanol
  • Glucose
  • Neuroprotective Agents / pharmacology*
  • Oxidative Stress
  • Oxygen
  • PC12 Cells
  • Plant Extracts / pharmacology*
  • Poly (ADP-Ribose) Polymerase-1 / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • bcl-2-Associated X Protein / metabolism

Substances

  • Bax protein, rat
  • Bcl2 protein, rat
  • Neuroprotective Agents
  • Plant Extracts
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Ethanol
  • Parp1 protein, rat
  • Poly (ADP-Ribose) Polymerase-1
  • Casp3 protein, rat
  • Caspase 3
  • Glucose
  • Oxygen