4.5 Article

Oxymatrine protects against myocardial injury via inhibition of JAK2/STAT3 signaling in rat septic shock

Journal

MOLECULAR MEDICINE REPORTS
Volume 7, Issue 4, Pages 1293-1299

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/mmr.2013.1315

Keywords

oxymatrine; septic shock; myocardial injury; JAK2/STAT3

Funding

  1. Natural Science Foundation of Ningxia [NZ1194]
  2. National Natural Science Foundation of China [30960108, 31060140, 31260243]
  3. Yinchuan Key Scientific and Technological Project for Minghao Zhang
  4. Key Project of Department of Public Health of Ningxia [2012004]
  5. SRF for ROCS, SEM

Ask authors/readers for more resources

Oxymatrine (OMT), an alkaloid extracted from Sophora japonica (kushen), is used to treat inflammatory diseases and various types of cancer in traditional Chinese medicine. However, the cellular and molecular mechanisms underlying the anti-inflammatory activity of OMT remain poorly understood. The present study explored the protective effect of OMT on myocardial injury in rats with septic shock by inhibiting the activation of the janus kinase-signal transducer and activator of transcription (JAK/STAT) signaling pathway. OMT treatment was found to significantly inhibit the activation of JAK2 and STAT3 in myocardial tissue. It also attenuated the expression of pro-inflammatory cytokines, including interleukin-1 beta and tumor necrosis factor-alpha. In addition, OMT exhibited anti-inflammatory properties as heart function and myocardial contractility was improved and pathological and ultrastructural injury was prevented in myocardial tissue induced by septic shock. The results indicate that OMT exhibits substantial therapeutic potential for the treatment of septic shock-induced myocardial injury through inhibition of the JAK2/STAT3 signaling pathway.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available