The protective effects of ethanolic extract of Clematis terniflora against corticosterone-induced neuronal damage via the AKT and ERK1/2 pathway

BMB Rep. 2018 Aug;51(8):400-405. doi: 10.5483/BMBRep.2018.51.8.099.

Abstract

Chronic stress induces neuronal cell death, which can cause nervous system disorders including Parkinson's disease and Alzheimer's disease. In this study, we evaluated the neuroprotective effects of Clematis terniflora extract (CTE) against corticosterone-induced apoptosis in rat pheochromocytoma (PC12) cells, and also investigated the underlying molecular mechanisms. At concentrations of 300 and 500 μg/ml, CTE significantly decreased apoptotic cell death and mitochondrial damage induced by 200 μM corticosterone. CTE decreased the expression levels of endoplasmic reticulum (ER) stress proteins GRP78, GADD153, and mitochondrial damage-related protein BAD, suggesting that it downregulates ER stress evoked by corticosterone. Furthermore, our results suggested that these protective effects were mediated by the upregulation of p-AKT and p-ERK1/2, which are involved in cell survival signaling. Collectively, our results indicate that CTE can lessen neural damage caused by chronic stress. [BMB Reports 2018; 51(8): 400-405].

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cell Death / drug effects
  • Cell Survival / drug effects
  • Clematis / chemistry*
  • Corticosterone / pharmacology
  • Endoplasmic Reticulum Stress / drug effects
  • MAP Kinase Signaling System / drug effects*
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Neuroprotective Agents / pharmacology*
  • PC12 Cells
  • Plant Extracts / pharmacology*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects

Substances

  • Neuroprotective Agents
  • Plant Extracts
  • Reactive Oxygen Species
  • Proto-Oncogene Proteins c-akt
  • Corticosterone