Reduction of Ischemic Brain Edema by Combined use of Paeoniflorin and Astragaloside IV via Down-Regulating Connexin 43

Phytother Res. 2017 Sep;31(9):1410-1418. doi: 10.1002/ptr.5868. Epub 2017 Jul 28.

Abstract

Paeoniflorin (PF) and astragaloside IV (AS-IV) have protective effects on cerebral ischemia. We aimed to test the effects of combined use of PF and AS-IV on ischemic brain edema and investigate whether the effects were dependent on connexin43 (Cx43). We detected the expression of Cx43 induced by PF and AS-IV after cerebral ischemia. We also examined the effects of combined use of PF and AS-IV on ischemic edema and further investigated the related pathways. We demonstrated PF and AS-IV decreased Cx43 and aquaporin4 (AQP4) associating with reduction of brain edema by dry-wet weight and brain-specific gravity methods after cerebral ischemia. Administration of PF and AS-IV displayed a further attenuation of brain edema with lower Cx43 levels. Meanwhile, Cx43 blockade inhibited AQP4 down-regulation by the two drugs. Moreover, phosphorylation of C-Jun amino-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) were increased by PF and AS-IV, respectively. The effects of PF and AS-IV to down-regulate Cx43 were suppressed by JNK and ERK inhibitors, respectively. Our data indicate that PF and AS-IV alleviate ischemic brain edema, which has close relation to Cx43 down-regulation causing decrease of AQP4 via JNK and ERK pathways activation, respectively. Combined administration elicits synergistic effects on brain edema reduction. Copyright © 2017 John Wiley & Sons, Ltd.

Keywords: aquaporin4; astragaloside IV; brain edema; cerebral ischemia; connexin43; paeoniflorin.

MeSH terms

  • Animals
  • Aquaporin 4 / metabolism
  • Brain Edema / drug therapy*
  • Brain Ischemia / drug therapy
  • Connexin 43 / metabolism*
  • Down-Regulation
  • Drug Synergism
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Glucosides / pharmacology*
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Male
  • Monoterpenes / pharmacology*
  • Rats, Sprague-Dawley
  • Saponins / pharmacology*
  • Signal Transduction / drug effects
  • Triterpenes / pharmacology*

Substances

  • Aqp4 protein, rat
  • Aquaporin 4
  • Connexin 43
  • Gja1 protein, rat
  • Glucosides
  • Monoterpenes
  • Saponins
  • Triterpenes
  • peoniflorin
  • astragaloside A
  • Extracellular Signal-Regulated MAP Kinases
  • JNK Mitogen-Activated Protein Kinases