Use of STAT1 inhibitors in the treatment of brain I/R injury and neurodegenerative diseases

Cent Nerv Syst Agents Med Chem. 2011 Mar 1;11(1):2-7. doi: 10.2174/187152411794961077.

Abstract

In the etiology of brain injury associated to ischemia/reperfusion (I/R) and neurodegenerative diseases, a critical involvement of excessive activation of signal transducer and activator of transcription 1 (STAT1) and successive induction of iNOS expression has widely been evidenced. Any compound capable to down-regulate STAT1 activation seems to represent a new, promising anti-inflammatory drug. Among plant compounds, only a few have shown to possess anti-STAT1 activity. Among them, epigallocatechin-3-gallate (EGCG), the main polyphenol present in green tea leaves, efficiently protects heart from I/R injury and this action is strictly correlated to its anti-STAT1 property. Hyperforin, the non-polyphenolic compound present in St. John's wort, attenuates β-cell death induced by interferon-γ (IFN-γ) by strongly down-regulating STAT1 activation. STAT1, therefore, seems to represent a new molecular target of the protective treatment also against brain injury associated to a number of brain pathologies. Either understanding the molecular mechanism of anti-STAT1 action of these compounds or identification of other anti-STAT1 compounds are urged.

Publication types

  • Review

MeSH terms

  • Animals
  • Brain / pathology*
  • Bridged Bicyclo Compounds / chemistry
  • Bridged Bicyclo Compounds / therapeutic use
  • Catechin / analogs & derivatives
  • Catechin / chemistry
  • Catechin / therapeutic use
  • Humans
  • Janus Kinases / metabolism
  • Molecular Structure
  • Neurodegenerative Diseases / drug therapy*
  • Neurodegenerative Diseases / pathology
  • Neuroprotective Agents / chemistry
  • Neuroprotective Agents / therapeutic use
  • Phloroglucinol / analogs & derivatives
  • Phloroglucinol / chemistry
  • Phloroglucinol / therapeutic use
  • Reperfusion Injury / drug therapy*
  • Reperfusion Injury / pathology
  • STAT1 Transcription Factor / antagonists & inhibitors*
  • STAT1 Transcription Factor / metabolism
  • Signal Transduction
  • Terpenes / chemistry
  • Terpenes / therapeutic use

Substances

  • Bridged Bicyclo Compounds
  • Neuroprotective Agents
  • STAT1 Transcription Factor
  • Terpenes
  • Catechin
  • epigallocatechin gallate
  • Phloroglucinol
  • Janus Kinases
  • hyperforin