The neuroprotective effects of an extract of Gastrodia elata

J Ethnopharmacol. 2011 Oct 31;138(1):119-25. doi: 10.1016/j.jep.2011.08.064. Epub 2011 Sep 8.

Abstract

Ethnopharmacological relevance: Gastrodia elata (GE) Blume (family Orchidaceae) is a traditional Chinese herbal medicine for treating headaches, dizziness, tetanus, and epilepsy, indicating neuronal protective functions.

Aim of the study: To evaluate the neuroprotection of GE and its molecular mechanism in preventing serum deprivation-induced PC12 cell apoptosis.

Materials and methods: An MTT assay and Hoechst staining were used to respectively validate serum deprivation-induced cell death and apoptosis. Cyclic (c)AMP formation and protein kinase (PK)A activity were also measured after GE treatment. Western blotting was used to detect the phosphorylation of the cAMP response element-binding (CREB) protein. Transient transfection of a dominant negative CREB was used to validate the importance of CREB.

Results: GE targeted the adenosine A(2A) receptor (A(2A)-R). GE increased cAMP formation, PKA activity, and phosphorylation of the CREB protein. GE-induced CREB protein phosphorylation and protection was blocked by a PKA inhibitor and overexpression of the dominant negative CREB, respectively.

Conclusions: These results support the neuroprotective effects of GE. The protective mechanism might be mediated through an A(2A)-R/cAMP/PKA/CREB-dependent pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine A2 Receptor Agonists / isolation & purification
  • Adenosine A2 Receptor Agonists / pharmacology*
  • Animals
  • Apoptosis / drug effects*
  • Cyclic AMP / biosynthesis
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Gastrodia* / chemistry
  • Neuroprotective Agents / isolation & purification
  • Neuroprotective Agents / pharmacology*
  • PC12 Cells
  • Phosphorylation
  • Plant Extracts / pharmacology*
  • Rats
  • Receptors, Adenosine A2 / metabolism*

Substances

  • Adenosine A2 Receptor Agonists
  • Cyclic AMP Response Element-Binding Protein
  • Neuroprotective Agents
  • Plant Extracts
  • Receptors, Adenosine A2
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases